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Fe i Oscillator Strengths for Transitions from High-lying Odd-parity Levels

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Published 2017 October 23 © 2017. The American Astronomical Society. All rights reserved.
, , Citation M. T. Belmonte et al 2017 ApJ 848 125 DOI 10.3847/1538-4357/aa8cd3

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0004-637X/848/2/125

Abstract

We report new experimental Fe i oscillator strengths obtained by combining measurements of branching fractions measured with a Fourier Transform spectrometer and time-resolved, laser-induced fluorescence lifetimes. This study covers the spectral region ranging from 213 to 1033 nm. A total of 120 experimental $\mathrm{log}({gf})$-values coming from 15 odd-parity energy levels are provided, 22 of which have not been reported previously and 63 of which have values with lower uncertainty than the existing data. The radiative lifetimes for 60 upper energy levels are presented, 39 of which have no previous measurements.

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1. Introduction

Iron is one of the most-studied elements within the field of astronomy due to its important presence in stellar spectra. With a very complex spectrum, neutral iron presents thousands of transitions across a very wide spectral range, from the ultraviolet to the infrared. A very comprehensive study of its spectrum was undertaken by Nave et al. (1994), which provides an extremely useful guide for the identification of Fe i spectral lines in astronomical spectra. However, of the 6758 lines included in the National Institute of Standards and Technology (NIST) atomic database (Kramida et al. 2011) in the spectral interval ranging from 200 to 1050 nm, only a small percentage possess accurate values of transition probabilities.

Atomic oscillator strengths (transition probabilities, log $({gf})$) are essential to model stellar line intensities and to calculate not only chemical abundances, but also other stellar parameters. In particular, the iron spectrum is of the utmost importance to obtain stellar metallicities, as this property is directly linked to the iron abundance. However, the quantity and quality of the existing data lies far from the current needs of the astronomical community, remaining the Achilles' heel of the field of Galactic archeology (Bigot & Thévenin 2006). Several attempts have been made to assemble comprehensive line lists with reliable atomic data (Heiter et al. 2015b) that can be used as a standard input for the different local thermodynamic equilibrium (LTE) and non-LTE models used to determine chemical abundances.

Several studies regarding the measurement of oscillator strengths of neutral iron have been conducted over the last 50 years. A very detailed review of the situation was carried out 11 years ago by Fuhr & Wiese (2006), who presented the most comprehensive compilation of Fe i transition probabilities to date, which states clearly the need for new studies that complete and improve the quality of thousands of spectral lines in the database of Fe i log $({gf})$ values. Among all the works whose values are included in Fuhr & Wiese (2006), two deserve special attention due to the quality of their results and their coverage: the experiments conducted by Blackwell et al. (1979a, 1979b, 1980, 1982a, 1982b, 1986) and O'Brian et al. (1991).

Very accurate absorption oscillator strengths were obtained by Blackwell et al. from a very stable light source in an absorption experiment, with estimated uncertainties lower than ±4% on an absolute scale. Their values are generally considered as the most reliable ones by Fuhr & Wiese (2006), who rated them as "A" in their compilation. The comprehensive work from O'Brian et al. (1991) provides accurate transition probabilities for 1814 spectral lines of neutral iron obtained in an emission experiment by using two different methods. One method combines radiative lifetimes of 186 energy levels with measurements of branching fractions yielding 1174 absolute transition probabilities. The other method used by O'Brian et al. interpolated the populations of energy levels using those with known lifetimes in an inductively coupled plasma source, producing 640 extra transition probabilities with uncertainties that they estimated to be lower than ±10%. Within the spectral range included in our new study, the majority of the log $({gf})$-values available for comparison belong to O'Brian et al. (1991).

The present work is the third in a series of articles published as a result of the collaboration between the Fourier Transform Spectroscopy laboratory at Imperial College London (IC) and the University of Wisconsin-Madison (UW). It completes the previous works on log $({gf})$ for Fe i lines of interest in the Gaia-ESO survey (Ruffoni et al. 2014) and oscillator strengths for transitions coming from high-lying even-parity Fe i levels (Den Hartog et al. 2014). In this paper, we focus on the log $({gf})$ values for transitions coming from high-lying odd-parity upper energy levels, four of which contain spectral lines of particular interest for the Gaia-ESO survey. We provide new radiative lifetimes for 60 high-lying odd-parity levels obtained at the UW, 39 of which are measured for the first time. Fe i emission spectra were recorded with the Fourier transform spectrometers (FTSs) at IC and at the NIST. Measurements of branching fractions were completed for 15 of the previously mentioned odd-parity levels, and were combined with the new lifetimes to obtain 120 accurate values of oscillator strengths (and transition probabilities). Comparison with previous experiments shows that 22 of the analyzed transitions have no earlier log $({gf})$-values and for 63 transitions the accuracy of the log $({gf}){\rm{s}}$ are improved compared with existing measurements in the literature.

2. Experimental Procedure

Oscillator strengths, or absorption f-values, are obtained experimentally from the measurement of atomic transition probabilities, Aul, where the subscript ul refers to the transition from a given upper energy level, u, to a lower level, l. Transition probabilities and absorption f-values are related by (Thorne et al. 2007)

Equation (1)

where gl and gu are the statistical weights of the lower and upper energy level, respectively, and λ is the wavelength of the line expressed in nm.

The transition probability of a given atomic transition can be obtained spectroscopically, because in the case of an optically thin plasma, it is proportional to the area under the profile of the corresponding spectral line. The integrated area of each intensity calibrated spectral line, Iul, is proportional to its intensity in photons per second (Pickering et al. 2001a).

So-called branching fractions (Huber & Sandeman 1986) are given by

Equation (2)

and for a particular upper energy level, the lifetime ${\tau }_{u}$ is

Equation (3)

As long as the sum of the Aul includes all branches to the lower energy levels, we can combine expressions (2) and (3) to obtain the transition probability of a given transition as

Equation (4)

As can be seen, this method of measuring Aul has the advantage that no assumption needs to be made regarding the thermodynamic equilibrium of the plasma used as a light source.

2.1. Branching Fraction Measurements

Two different sets of spectra were used to obtain the log $({gf})$ values included in this work. Spectrum A was measured on the 2 m FTS at the NIST, and it covers the spectral range between 8000 and 26,000 cm−1. An iron cathode mounted in a water-cooled hollow cathode lamp (HCL) was used to generate the plasma used as light source. The HCL was run in Ne at a pressure of 2.1 mbar and a current 2 A. Detailed descriptions of this measurement can be found in Ruffoni et al. (2014) and Den Hartog et al. (2014). The response function of the spectrometer, shown in Figure 1 for Spectrum A, was obtained by using a calibrated standard tungsten (W) halogen lamp in the spectral range between 250 and 2400 nm. To verify that this spectrometer response was stable over time, spectra of this tungsten lamp (whose radiance is known to ±1.1%) were measured before and after acquiring iron spectra with the HCL.

Figure 1.

Figure 1. Response functions used to intensity calibrate the five different spectra used in this work (see Table 1).

Standard image High-resolution image

Spectra B, C, D, and G were measured on the 0.2 m VUV FTS at Imperial College, and they cover the spectral range between 20,000 and 62,000 cm−1. The resolution, detector, and filter used to record each spectrum, as well as the experimental conditions, are included in Table 1. The Fe i emission spectra were produced in a water-cooled HCL filled with Ne at a pressure ranging from 1.3 to 1.4 mbar and with a 99.8% pure iron cathode operated as the source. Currents of 700 or 1000 mA (see Table 1) were selected depending on the signal-to-noise ratio (S/N) of the spectral lines of interest. These conditions were optimized to obtain the highest S/N for the weaker lines, while avoiding self-absorption effects for the stronger lines.

Table 1.  FTS Spectra Used for the Branching Fraction Measurements

Spectrum Wavenumber Resolution Detector Filter P Gas I Lamp Spectrum
  Range Used (cm−1) (cm−1)     (mbar) (mA) File Namea
A (NIST) 9600–26000 0.02 Si diode None 2.1 2000 Fe0301to0403_Calib
B (IC) 21000–33000 0.037 R11568 PMT Schott BG3 1.3 700 F130610.002.047_Scaled
C (IC) 23000–41000 0.037 R11568 PMT UG5 1.4 700 Fe130624.011.039_Scaled
D (IC) 31000–47000 0.037 R7154 PMT None 1.3 1000 Fe130603.021.059_Calib
G (IC) 20000–35000 0.037 R11568 PMT Schott BG3 1.3 1000 Fe130604A.007.034

Note.

aSeveral spectra were coadded to improve the S/N of the spectral lines.

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Two standard intensity calibrated lamps were used to obtain the response function of the IC VUV spectrometer for these four spectra: a deuterium lamp (D2) in the spectral interval ranging from 200 to 350 nm and a tungsten lamp (W) for longward of 300 nm. Spectra from these two lamps were measured before and after each of the runs recorded with the HCL lamp and using the same measurement conditions. The uncertainties of the relative spectral radiance of the W lamp, calibrated by the UK National Physical Laboratory (NPL), were lower than ±1.4% between 410 and 800 nm, increasing to ±2.8% at 300 nm. The deuterium lamp, calibrated by the Physikalisch-Technische Bundesanstalt in Germany, has a relative spectral radiance with an uncertainty of ±7% between 170 and 410 nm. The response functions of the different spectra, shown in Figure 1, were obtained by combining the response functions found using both lamps, W and D2.

The Fe spectra were fitted by using Voigt profiles with the XGREMLIN package (Nave et al. 1997). Once fitted and intensity calibrated, the spectra were used to obtain the branching fractions of all the transitions coming from the upper energy levels of interest by using the FAST software package (Ruffoni et al. 2013b). The calculated branching fractions of Kurucz (2007) were used to define the transitions to be included, and to estimate the completeness of the set of transitions from each upper level considered, as described in Pickering et al. (2001a, 2001b). Final results for new log $({gf}){\rm{s}}$ were also obtained using the FAST software to combine the branching fractions with the new experimental upper energy lifetime values described in Section 2.2.

All of the fitted spectral lines were checked for possible self absorption by carefully examining the residuals from the line fits. Possible cases of blended lines were also analyzed by checking the Fe i line list of Nave et al. (1994) and Fe ii line list of Nave & Johansson (2013), as well as the theoretical log $({gf}){\rm{s}}$ of Kurucz (2007).

For most of the cases, more than one spectrum from Table 1 was necessary to encompass all the transitions coming from a given upper energy level. In these situations, all of the lines were put on a common relative intensity scale by calculating the ratio in the intensity of several lines from that particular upper energy level which were measured in the overlapping region of the pairs of spectra. A detailed description of this method can be found in Pickering et al. (2001a, 2001b).

We paid special attention to the calculation of the experimental uncertainties introduced in our BF measurements by taking into account all the different sources of error, such as the uncertainty in the S/N of the observed Fe i spectral line and the standard calibration lamp spectra, as well as the spectral radiance uncertainty of these standard light sources. A detailed description can be found in Ruffoni et al. (2013b) and Ruffoni (2013a), but the general expression is included here for completeness. The experimental uncertainty of a given BF can be defined as

Equation (5)

where Iul is the calibrated relative intensity of the emission line associated with the electronic transition from level u to level l, and ${\rm{\Delta }}{I}_{{ul}}$ is the uncertainty in intensity of this line due to its measured S/N and the uncertainty in the intensity of the standard lamp. From Equation (4), it then follows that the uncertainty in Aul is

Equation (6)

where ${\rm{\Delta }}{\tau }_{{ul}}$ is the uncertainty in our measured upper level lifetime. Finally, the uncertainty in $\mathrm{log}({gf})$ of a given line can be calculated as

Equation (7)

2.2. Radiative Lifetime Measurements

Radiative lifetimes provide the absolute scale for the branching fractions. They are measured using time-resolved laser-induced fluorescence (TRLIF) on a slow beam of iron atoms. This beam is produced from a hollow cathode discharge sputter source. A pulsed electrical discharge is operated in ∼50 Pa argon gas at 30 Hz repetition rate. The pulses have ∼10 A peak current and 10 μs duration during which the energetic argon ions sputter atoms from the pure iron foil lining the stainless steel hollow cathode. The discharge is maintained between pulses with a 30 mA DC current. The cathode is closed on the downstream end, except for a 1 mm flared hole, through which the gas phase iron is differentially pumped into the low pressure (∼10−2 Pa) scattering chamber. The beam is weakly collimated and slow (the neutrals have speeds of ∼5 × 104 cm s−1 and the ions are somewhat faster), and contains both neutral and singly ionized iron in their ground and low metastable levels.

The atomic/ionic beam is intersected at 90° angles by a beam from a nitrogen laser-pumped dye laser. This intersection takes place 1 cm below the bottom of the cathode. The laser pulse is delayed relative to the peak of the discharge pulse by ∼20 μs to account for the transit time of the atoms. The duration of the laser is ∼3 ns (FWHM) and the pulse terminates completely within a few nanoseconds. This latter characteristic allows the fluorescence to be recorded free from laser interaction, making it unnecessary to deconvolute the laser pulse and fluorescence signals. The wavelength of the laser is tunable over the range 205–720 nm using a large selection of dyes as well as frequency-doubling crystals. The narrow bandwidth of the laser (0.2 cm−1) ensures selective excitation of the level of interest. Cascade radiation from higher-lying levels, which troubled earlier, non-selective techniques such as beam foil excitation, is not a problem in this experiment.

A transition is chosen for laser excitation which is classified to the level of interest and has some observed intensity in the NIST line list for Fe i (Kramida et al. 2011). The transition must also originate in the ground or in low-lying metastable levels that are populated in the atomic beam. We find that neutral iron metastable levels up to 25,000 cm−1 have sufficient population for use as lower levels for laser excitation. Care must be taken to correctly identify the transition in the experiment, particularly when working in such dense spectra as Fe i, ii. We do not rely on an absolute measurement of the laser wavelength. Rather, the wavelength is course-tuned to within 0.1 nm of the transition by adjusting the grating of the dye laser while monitoring the wavelength with a 0.5 m focal length monochromator. An LIF spectrum is then recorded while the laser wavelength is slowly changed over a range of 0.5–1 nm. This fine control of the laser is accomplished by pressurizing an aluminum box that houses the laser grating up to 1300 kPa of nitrogen and then slowly bleeding the nitrogen away, changing the index of refraction. This low-tech method yields extremely linear and reproducible control of the laser wavelength. The separation between lines on the LIF spectrum can be measured accurately to ±0.002 nm. This spectrum is then pattern-matched to the NIST line list to correctly identify the transition of interest.

Once the laser wavelength is tuned to the transition, fluorescence is collected at right angles to both laser and atomic beams through a pair of fused-silica lenses. These lenses comprise an f/1 optical system. Allowance is made for the insertion of optical filters between the two lenses where the fluorescence is roughly collimated. These filters can be broadband colored-glass filters or narrowband multi-layer dielectric interference filters. Their function is to block scattered laser light, light from the discharge, and cascade radiation. Although cascade from higher levels is not a problem due to the selective nature of the excitation, cascade from lower-lying levels is still a possibility. Fluorescence from the beam interaction region is imaged onto the photocathode of a RCA 1P28A photomultiplier tube (PMT). The PMT signal is then recorded with a Tektronix SCD1000 transient digitizer beginning at least 7 ns after the peak of the laser pulse. This delay allows time for the complete termination of the laser so that deconvolution of the laser temporal profile from the fluorescence signal is not necessary. An average of 640 fluorescence decays is recorded. The laser wavelength is then tuned off the transition and an average of 640 background traces is recorded. These data are downloaded to a computer for analysis. The digitized data is divided into an early-time and a late-time section for analysis, each being ∼1.5 lifetimes in length. A least-squares-fit to a single exponential is performed on the background-subtracted signal to determine a lifetime in each section. Comparison of the early- and late-time lifetimes gives a quick and sensitive method to check for any systematic deviations from a clean exponential. Five such lifetime measurements are averaged together for a given set of experimental conditions. Two measurements of each lifetime are made with typically several months intervening and using a different laser transition whenever possible. This redundancy ensures that the experiment is running reproducibly, that the transitions are identified correctly in the experiment, that they are classified correctly to the upper level, and that they are not masked by a hidden blend or affected by cascade radiation through lower levels.

In addition to cascade radiation, there are several other effects that must be understood and controlled to ensure a clean lifetime measurement. The dynamic range of the experiment extends from ∼2 ns to several microseconds. The bandwidth of the PMT, digitizer, and associated electronics begins to affect the fidelity of the lifetime measurements below ∼4 ns and limits the minimum lifetime to ∼2 ns. We assign a minimum uncertainty of 0.2 ns, such that the fractional uncertainty rises from 5% at 4 ns up to 10% at 2 ns lifetime. The other end of the dynamic range is limited by the flight-out-of-view effect, where the motion of the atoms has taken those radiating later in the decay outside the view of the PMT. This has the effect of artificially shortening the measured lifetime. This effect can be mitigated somewhat by inserting a cylindrical lens in the optical train that serves to defocus the optics in the direction of motion, making them much less sensitive to that motion. This step is taken for neutral lifetimes >300 ns and ion lifetimes >100 ns (ions move somewhat faster than the neutrals). It also has the unfortunate effect of diminishing the signal levels by a factor of five or so. Zeeman quantum beats arise when the atomic dipoles excited by the polarized laser have time to precess in the Earth's magnetic field before they radiate. To avoid this effect, the region where the laser and atomic beams interact is placed at the center of a set of Helmholtz coils which are used to zero the field to within ±2 μT. This tolerance is adequate to avoid Zeeman quantum beats for shorter lifetimes, but for longer lifetimes (>300 ns), some effect can still be observed. In these cases, a high magnetic field (3 mT) is produced with a second set of coils which causes rapid precession and the Zeeman beats are washed out on the longer digitizer time windows employed. A further systematic effect arises from after-pulsing in the PMT. Generally, the characteristics of the 1P28A PMT, i.e., fast rise-time and high sensitivity in the UV and visible, are favorable for lifetime measurements. However, the PMT does produce a weak (0.1%) after-pulse as a result of the prompt electron cascade ionizing residual gas in the tube. This weak and relatively slow signal is picked up on the photocathode and results in a systematic, reproducible lengthening of lifetimes around 100 ns. This effect of a few percent is corrected for in the final lifetimes.

We periodically measure a set of benchmark lifetimes, which helps us ensure that the experiment is running reproducibly and accurately. These benchmarks are lifetimes that are well known from other sources. Some are from theoretical calculations and others from experiments which have smaller, and generally different systematic uncertainties than our own. The benchmarks measured for the current set of lifetimes are ${{\rm{z}}}^{6}{{\rm{F}}}_{11/2}$ and ${{\rm{z}}}^{6}{{\rm{D}}}_{9/2}$ states of Fe+ at 3.19(4) ns and 3.70(6) ns, respectively (laser-fast beam, Biémont et al. 1991), ${2}^{2}{{\rm{P}}}_{3/2}$ state of Be+ at 8.8519(8) ns (variational method calculation,Yan et al. 1998); the ${3}^{2}{{\rm{P}}}_{3/2}$ state of neutral Na at 16.23(1) ns (NIST critical compilation of Kelleher & Podobedova 2008); 4p'[1/2]1 state of Ar at 27.85(7) ns (beam-gas-laser-spectroscopy, Volz & Schmoranzer 1998); 33P, 43P, and 53P states of neutral He at 94.8(1) and 219.3(2) ns (variational method calculation, Kono & Hattori 1984; Drake & Morton 2007). These benchmarks allow us to quantify small corrections due to residual systematic effects, ensuring that our lifetimes are well within the stated uncertainty. A comparison of our lifetimes to laser-fast beam measurements performed by Scholl et al. (2002) in Sm II suggests that the stated uncertainties are conservative (Lawler et al. 2008).

3. Results and Discussion

In Table 2, we report the results of lifetime measurements from this study as well as LIF results from the literature. Lifetimes measured using older, less reliable techniques are not listed. Lifetimes are given for 60 high-lying odd-parity levels of Fe i ranging in energy from 27 166.82 to 57 565.31 cm−1. The fractional uncertainty in our measurements is 5%, except for those lifetimes less than 4 ns, for which the absolute uncertainty is 0.2 ns. Approximately two-thirds of these lifetimes are measured for the first time. The comparison with the earlier work is very favorable. The lifetimes in the O'Brian et al. (1991) work were measured in our (UW) lab with nearly the same apparatus as the current work (in the earlier work, a different digitizer was used). We re-measured some of the original O'Brian et al. (1991) lifetimes to ensure that, even after 25 years, the experiment is giving consistent results. Happily, we see very good agreement with this older work. For eight lifetimes in common, the mean and rms differences between the current study and O'Brian et al. (1991) are −1.5% and 3.1%, respectively, using the current study as reference (in the sense (theirs ours)/ours). The level of agreement with Engelke et al. (1993) is also very good with mean and rms differences of −1.1% and 5.4%, respectively. Our study overlaps with that of Marek et al. (1979) for only two lifetimes that agree within 0.5% for the longer lifetime around 64 ns and within 4.5% for a shorter lifetime around 9 ns. Our study overlaps with that of Langhans et al. (1995) for only two very short lifetimes less than 3 ns. We agree perfectly in one case and differ by only 0.1 ns for the other. The excellent level of agreement with these four earlier studies is typical of modern TRLIF measurements.

Table 2.  Radiative Lifetimes of Fe i Odd-parity Levels Including Many Higher Levels Studied for the First Time in Our Work

Configurationa Terma J Levela Laser Wavelengthsa Lifetime (ns)
      (cm−1) (nm) This Expt. Other Expt.
3d6(5D)4s4p(3Po) z5Fo 4 27166.82 505.1634, 514.2928 63.4 63.6b, 66.6c, 63.7(4.0)d
3d6(5D)4s4p(3Po) z5Po 3 29056.324 344.0605, 349.0573 43.7
3d6(5D)4s4p(3Po) z5Po 2 29469.024 344.0988, 347.5449 43.2
3d6(5D)4s4p(3Po) z5Po 1 29732.736 344.3876, 347.6701 42.6
3d7(4F)4p z5Go 6 34843.957 358.1192 9.2 9.6(0.6)d
3d6(5D)4s4p(1Po) x5Do 3 39969.853 250.1131, 445.9117 2.7 2.6b, 2.8c, 2.7(1)e
3d6(5D)4s4p(1Po) x5Do 1 40404.518 251.8101, 444.7716 2.8 2.6b, 2.9c, 2.7(1)e
3d5(6S)4s24p y7Po 4 40421.938 247.3156 317 309b
3d6(3F2)4s4p(3Po) v5Do 4 44022.525 227.0862, 229.2524 96.5 95.9b
3d6(3F2)4s4p(3Po) v5Do 1 44760.746 226.9098, 228.3303 21.3 21.4b
3d6(3F2)4s4p(3Po) w5Fo 4 44415.074 225.0790, 227.2069 41.6 41.2b
3d7(4P)4p y5So 2 44511.812 226.7084, 273.6963 13.3 13.6b
3d7(4P)4p w5Po 3 46137.097 216.6773, 218.6486 3.2
3d7(4P)4p w5Po 2 46313.537 219.1839, 220.0724 3.2
3d7(4P)4p w5Po 1 46410.381 218.7194, 219.6041 3.5
3d6(3P2)4s4p(3Po) z3So 1 46600.818 218.6892, 219.1204 16.5
3d6(3P2)4s4p(3Po) y3Po 2 46727.074 215.8629, 344.7277 19
3d6(3P2)4s4p(3Po) y3Po 1 46901.832 217.2584, 217.6840 11
3d7(4P)4p u5Do 4 46720.842 213.9697, 215.8919 12.2
3d7(4P)4p u5Do 3 46744.993 215.7794, 217.1296 9.9
3d7(4P)4p u5Do 2 46888.517 216.4548, 217.3213 11.4
3d7(4P)4p u5Do 0 47171.531 215.9923, 341.8507 7.8
3d7(4P)4p u5Do 1 47177.234 216.3862, 341.7840 9.8 9.3c
3d6(3F2)4s4p(3Po) x3Fo 4 46889.142 213.2016, 250.1693 11.1 10.7c
3d6(3F2)4s4p(3Po) x3Fo 3 47092.712 214.1718, 215.5019 18.2 17.4c
3d6(3F2)4s4p(3Po) x3Fo 2 47197.01 215.0184, 215.8734 22.9 21.8c
3d7(4P)4p w3Do 3 47017.188 214.5189, 215.8534 11.6 11.5c
3d7(4P)4p w3Do 2 47136.084 215.3006, 216.1579 11.9 11.7c
3d7(4P)4p w3Do 1 47272.027 214.6720, 215.5243 14.2 15.1c
3d6(3P2)4s4p(3Po) 1Do 2 47419.687 213.9934, 214.8403 33
3d7(2G)4p z1Go 4 47452.717 251.6570, 388.4358 66.2 59.7c
3d6(3G)4s4p(3Po) v5Fo 5 47606.114 245.7596, 386.1343 27.8
3d6(3G)4s4p(3Po) v5Fo 4 47929.997 246.5149, 248.6691 16.8
3d6(3G)4s4p(3Po) v5Fo 3 48122.928 245.3475, 247.4814 12.9
3d6(3G)4s4p(3Po) v5Fo 2 48238.847 209.0383, 248.3533 11.2 11.2c
3d6(3G)4s4p(3Po) v5Fo 1 48350.606 247.6656, 248.7065 11.2
3d5(6S)4s24p v5Po 3 47966.585 208.4121, 210.2353 6.3
3d5(6S)4s24p v5Po 2 48163.446 209.3684, 210.6394 6.4
3d5(6S)4s24p v5Po 1 48289.871 210.0797, 210.8958 5.9
3d7(4P)4p x3Po 2 48304.643 208.7510, 210.8301 12.7
3d7(4P)4p x3Po 1 48516.138 209.8938, 210.2910 10.7 10.6c
3d7(2G)4p z1Ho 5 48382.603 412.0206, 419.9094 16.2
3d7(2G)4p w3Fo 4 49108.896 239.5505, 269.2248 16.7
3d7(2G)4p w3Fo 3 49242.886 366.952 18.7
3d7(2G)4p w3Fo 2 49433.131 367.7627 12.8
3d7(2G)4p z1Fo 3 50586.878 384.3256 18.5
3d6(5D)4s(6D)5p u5Fo 5 51016.66 226.7469 20.6
3d6(5D)4s(6D)5p u5Fo 4 51381.457 224.8860, 227.1782 21.8
3d6(5D)4s(6D)5p t5Do 4 51076.628 226.4389, 228.7631 16.4
3d7(2H)4p u3Go 5 51373.91 253.7458, 337.0783 14.5 15.4c
3d7(2H)4p u3Go 4 51668.186 311.9494, 336.9547 15.2 13.5c
3d7(4F)5p 5Go 6 53069.357 216.6585 55.5
3d7(4F)5p 5Go 4 53852.114 216.7386, 238.7282 30.3
3d7(4F)5p 5Fo 5 53084.789 216.5861 25.5
3d7(4F)5p 5Fo 4 53388.637 215.1695, 217.2670 21.9
3d7(2H)4p 1Io 6 53093.529 373.8304, 411.8544 10.6
3d7(4F)5p 3Fo 3 54289.034 213.0965, 214.7045 19.8
3d6(3D)4s4p(3Po) 5Do 1 53975.744 218.1721, 277.3232 18.2
3d6(3D)4s4p(3Po) 5Do 4 54301.34 211.0235, 272.0196 19
3d6(3P2)4s4p(1Po) 3Do 3 57565.305 219.2823, 255.1093 6.3

Notes. The uncertainty in our measurements is the larger of ±5% or ±0.2 ns.

aConfigurations, terms, level energies, and Ritz wavelengths are from the NIST Atomic Spectra Database (http://www.nist.gov/pml/data/asd.cfm). bO'Brian et al. (1991) TRLIF with uncertainties equal to the larger of ±5% or ±0.2 ns. cLanghans et al. (1995) TRLIF with uncertainties of ±10% for lifetimes <3 ns and ±5% for the remainder. dMarek et al. (1979) delayed coincidence after laser excitation. eLanghans et al. (1995).

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Measurements of branching fractions were attempted for all the transitions coming from the upper energy levels included in Table 2 and completed for 15 of them. These upper energy levels are listed in Table 3 together with their configuration, the lifetime of the level used for the determination of the $\mathrm{log}({gf}){\rm{s}}$ and the completeness of each set of transitions. The remaining energy levels were excluded from our study due to the impossibility of putting the different lines onto a common intensity scale or to the presence of blended or very low S/N lines. Table 4 lists the results for branching fractions, transition probabilities, and $\mathrm{log}({gf}){\rm{s}}$ with their uncertainties for 120 transitions of Fe i, 22 of which are new and 63 have improved uncertainties compared with existing data. The spectral lines are grouped by common upper energy level and each set is sorted in order of descending wavelength. The values of the air wavelengths, as well as the upper and lower energy levels and J were taken from Kramida et al. (2011) based on Nave et al. (1994). In addition, the log $({gf}){\rm{s}}$ measured in this experiment are compared when possible with the value recommended by Fuhr & Wiese (2006), included in the last column along with the reference from the work from which the oscillator strength was taken. The letters L and P are used to indicate the method used in the O'Brian work to obtain these values and stand for "lifetime" and "population method," respectively.

Table 3.  Completeness of the Set of Transitions from each Upper Level Estimated By Using the Calculated Branching Fractions of Kurucz (2007)

Energy Level (cm−1)a Configuration Levela Lifetime Used (ns)b Completeness (%)c
34843.957 3d7(4F)4p z 5Go 9.2 100
39969.853 3d6(5D)4s4p(1Po) x5Do 2.7 99
40404.518 3d6(5D)4s4p(1Po) x5Do 2.8 99
44022.525 3d6(3F2)4s4p(3Po) v5Do 96.5 99
44415.074 3d6(3F2)4s4p(3Po) w5Fo 41.6 99
44760.746 3d6(3F2)4s4p(3Po) v5Do 21.3 98
46720.842 3d7(4P)4p u5Do 12.2 98
46889.142 3d6(3F2)4s4p(3Po) x3Fo 11.1 91
47092.712 3d6(3F2)4s4p(3Po) x3Fo 18.2 96
47197.010 3d6(3F2)4s4p(3Po) x3Fo 22.9 82
48350.606 3d6(3G)4s4p(3Po) v5Fo 11.2 94
48382.603 3d7(2G)4p z1Ho 16.2 99
50586.878 3d7(2G)4p z1Fo 18.5 94
51373.910 3d7(2H)4p u3Go 14.5 94
53093.529 3d7(2H)4p 1Io 10.6 98

Notes.

aThe energy and configuration levels are taken from Kramida et al. (2011). bExperimental lifetimes measured in this work. The uncertainty of these values is the larger of ±5% or ±0.2 ns. cCompleteness of the set of transitions from each upper energy level estimated as described in Pickering et al. (2001a, 2001b) by using the calculated branching fractions of Kurucz (2007).

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Table 4.  Experimental BFs, Transition Probabilities, and log $({gf})$ Values for 16 Odd-parity Energy Levels of Fe i

Wavelengtha Upper Levela Lower Levela BFb UBFb Aulc This Experimentd Publishede
(nm) E (cm−1) J E (cm−1) J   (%) (106 s−1) $\mathrm{log}({gf})$ $\mathrm{log}({gf})$ References
358.1193 34843.957 6 6928.268 5 1.0000 0.00 108.70 (5) 0.43 ± 0.02 0.406 ± 0.005 BL79
463.0120 39969.853 3 18378.185 2 0.0003 11.9 0.12 (13) −2.58 ± 0.05 −2.59 ± 0.12 OB91 L
449.4563 39969.853 3 17726.987 2 0.0090 3.4 3.44 (6) −1.14 ± 0.03 −1.14 ± 0.01 BL82a
445.9117 39969.853 3 17550.180 3 0.0065 3.2 2.49 (6) −1.29 ± 0.03 −1.28 ± 0.01 BL82a
312.5651 39969.853 3 7985.784 2 0.0049 7.5 1.90 (9) −1.71 ± 0.04 −1.66 ± 0.08 OB91 L
310.0665 39969.853 3 7728.059 3 0.0362 5.9 13.94 (8) −0.85 ± 0.03 −0.87 ± 0.08 OB91 L
306.7244 39969.853 3 7376.764 4 0.0999 5.6 38.42 (8) −0.42 ± 0.03 −0.51 ± 0.07 OB91 L
254.5978 39969.853 3 704.007 2 0.1858 5.1 71.44 (7) −0.31 ± 0.03 −0.31 ± 0.05 OB91 L
252.7435 39969.853 3 415.933 3 0.4774 3.1 183.63 (6) 0.090 ± 0.03 0.11 ± 0.04 OB91 L
250.1132 39969.853 3 0.000 4 0.1794 5.2 69.00 (7) −0.34 ± 0.03 −0.35 ± 0.05 OB91 L
444.7717 40404.518 1 17927.381 1 0.0138 4.0 4.94 (6) −1.36 ± 0.03 −1.34 ± 0.01 BL82a
440.8414 40404.518 1 17726.987 2 0.0058 5.5 2.08 (8) −1.74 ± 0.03 −1.78 ± 0.12 OB91 L
309.9895 40404.518 1 8154.713 1 0.0417 6.0 14.91 (8) −1.19 ± 0.03 −1.08 ± 0.05 OB91 L
308.3741 40404.518 1 7985.784 2 0.0655 5.9 23.41 (8) −1.00 ± 0.03 −0.88 ± 0.05 OB91 L
253.5607 40404.518 1 978.074 0 0.2678 4.7 95.63 (7) −0.56 ± 0.03 −0.56 ± 0.04 OB91 L
252.9835 40404.518 1 888.132 1 0.0881 6.9 31.48 (9) −1.04 ± 0.04 −0.96 ± 0.04 OB91 L
251.8102 40404.518 1 704.007 2 0.5167 2.9 184.54 (6) −0.28 ± 0.02 −0.26 ± 0.03 OB91 L
377.6455 44022.525 4 17550.180 3 0.1061 3.8 1.10 (6) −1.68 ± 0.03 −1.49 ± 0.05 OB91 L
275.4427 44022.525 4 7728.059 3 0.1559 4.8 1.62 (7) −1.78 ± 0.03 −1.78 ± 0.03 OB91 L
272.8021 44022.525 4 7376.764 4 0.3310 3.8 3.43 (6) −1.46 ± 0.03 −1.46 ± 0.03 OB91 L
269.5036 44022.525 4 6928.268 5 0.0438 5.5 0.45 (8) −2.35 ± 0.03 −2.33 ± 0.03 OB91 L
229.2525 44022.525 4 415.933 3 0.3122 4.0 3.24 (6) −1.64 ± 0.03 −1.68 ± 0.03 OB91 L
227.0863 44022.525 4 0.000 4 0.0484 6.0 0.50 (8) −2.46 ± 0.03
372.1272 44415.074 4 17550.180 3 0.0339 15.3 0.81 (16) −1.82 ± 0.07 −1.79 ± 0.05 OB91 L
272.4953 44415.074 4 7728.059 3 0.1987 4.6 4.78 (7) −1.32 ± 0.03 −1.32 ± 0.03 OB91 L
269.9107 44415.074 4 7376.764 4 0.2315 4.4 5.57 (7) −1.26 ± 0.03 −1.26 ± 0.02 OB91 L
266.6812 44415.074 4 6928.268 5 0.3765 3.6 9.05 (6) −1.061 ± 0.03 −1.07 ± 0.02 OB91 L
227.2070 44415.074 4 415.933 3 0.1170 5.1 2.81 (7) −1.71 ± 0.03 −1.69 ± 0.02 OB91 L
225.0790 44415.074 4 0.000 4 0.0419 6.3 1.01 (8) −2.16 ± 0.03 −2.08 ± 0.05 OB91 L
273.0982 44760.746 1 8154.713 1 0.1185 6.0 5.56 (8) −1.73 ± 0.03 −1.68 ± 0.02 OB91 L
271.8436 44760.746 1 7985.784 2 0.7738 1.4 36.33 (5) −0.92 ± 0.02 −0.90 ± 0.02 OB91 L
228.3304 44760.746 1 978.074 0 0.0510 8.3 2.39 (10) −2.25 ± 0.04 −2.22 ± 0.02 OB91 L
226.9099 44760.746 1 704.007 2 0.0383 10.5 1.80 (12) −2.38 ± 0.05
1033.3185 46720.842 4 37045.932 4 0.0010 12.8 0.09 (14) −1.91 ± 0.06
721.9682 46720.842 4 32873.630 4 0.0065 6.9 0.53 (9) −1.43 ± 0.04
451.4184 46720.842 4 24574.653 4 0.0049 11.2 0.40 (12) −1.96 ± 0.05 −1.92 ± 0.18 MA74
435.8501 46720.842 4 23783.617 5 0.0129 5.4 1.06 (7) −1.57 ± 0.03 −1.68 ± 0.05 OB91 P
399.8052 46720.842 4 21715.731 5 0.0875 4.7 7.17 (7) −0.81 ± 0.03 −0.91 ± 0.04 OB91 P
383.3308 46720.842 4 20641.109 4 0.0647 5.1 5.30 (7) −0.98 ± 0.03 −1.032 ± 0.004 BL82b
342.7120 46720.842 4 17550.180 3 0.6593 1.9 54.04 (5) −0.067 ± 0.02 −0.10 ± 0.04 OB91 P
287.7301 46720.842 4 11976.238 4 0.0544 7.2 4.46 (9) −1.30 ± 0.04 −1.29 ± 0.04 OB91 P
254.0916 46720.842 4 7376.764 4 0.0067 14.0 0.55 (15) −2.32 ± 0.06
251.2275 46720.842 4 6928.268 5 0.0352 7.2 2.89 (9) −1.61 ± 0.04 −1.73 ± 0.06 OB91 P
215.8920 46720.842 4 415.933 3 0.0128 13.4 1.05 (14) −2.18 ± 0.06
213.9698 46720.842 4 0.000 4 0.0369 8.7 3.02 (10) −1.73 ± 0.04
553.2747 46889.142 4 28819.952 5 0.0035 14.5 0.31 (15) −1.89 ± 0.06 −2.10 ± 0.30 MA74
493.4084 46889.142 4 26627.607 4 0.0014 17.9 0.13 (19) −2.39 ± 0.07
448.0137 46889.142 4 24574.653 4 0.0048 11.7 0.43 (13) −1.93 ± 0.05 −1.93 ± 0.09 OB91 P
432.6753 46889.142 4 23783.617 5 0.0068 9.8 0.62 (11) −1.81 ± 0.05 −1.93 ± 0.09 OB91 P
397.1322 46889.142 4 21715.731 5 0.0583 8.6 5.25 (10) −0.95 ± 0.04 −0.98 ± 0.04 OB91 P
380.8729 46889.142 4 20641.109 4 0.0387 8.9 3.48 (10) −1.17 ± 0.04 −1.159 ± 0.004 BL82b
340.7460 46889.142 4 17550.180 3 0.6629 2.8 59.72 (6) −0.029 ± 0.02 −0.02 ± 0.04 OB91 P
286.3430 46889.142 4 11976.238 4 0.0462 7.3 4.16 (9) −1.34 ± 0.04 −1.34 ± 0.04 OB91 P
250.1694 46889.142 4 6928.268 5 0.0524 7.4 4.72 (9) −1.40 ± 0.04 −1.51 ± 0.05 OB91 P
213.2017 46889.142 4 0.000 4 0.0386 9.3 3.48 (11) −1.67 ± 0.04 −1.33 ± 0.06
730.7931 47092.712 3 33412.715 3 0.0228 5.7 1.26 (8) −1.15 ± 0.03 −1.53 ± 0.06 OB91 P
435.1544 47092.712 3 24118.817 4 0.0210 4.7 1.15 (7) −1.64 ± 0.03 −1.73 ± 0.04 OB91 P
412.1802 47092.712 3 22838.321 2 0.0539 3.9 2.96 (6) −1.28 ± 0.03 −1.45 ± 0.04 OB91 P
398.3956 47092.712 3 21999.129 4 0.1291 3.5 7.09 (6) −0.93 ± 0.03 −1.02 ± 0.04 OB91 P
383.7135 47092.712 3 21038.986 2 0.0177 5.4 0.97 (7) −1.82 ± 0.03 −1.78 ± 0.09 OB91 P
381.3058 47092.712 3 20874.481 3 0.1163 2.9 6.39 (6) −1.01 ± 0.02 −1.07 ± 0.04 OB91 P
377.9416 47092.712 3 20641.109 4 0.0112 10.8 0.61 (12) −2.036 ± 0.05 −1.99 ± 0.05 OB91 P
340.4354 47092.712 3 17726.987 2 0.2180 4.3 11.98 (7) −0.84 ± 0.03 −0.88 ± 0.04 OB91 P
338.3979 47092.712 3 17550.180 3 0.1494 4.8 8.21 (7) −1.006 ± 0.03 −1.11 ± 0.04 OB91 P
292.9618 47092.712 3 12968.553 2 0.0135 11.2 0.74 (12) −2.18 ± 0.05 −2.22 ± 0.05 OB91 P
289.5035 47092.712 3 12560.933 3 0.1089 6.5 5.98 (8) −1.28 ± 0.03 −1.43 ± 0.04 OB91 P
284.6830 47092.712 3 11976.238 4 0.0164 9.0 0.90 (10) −2.12 ± 0.04 −2.13 ± 0.04 OB91 P
253.9587 47092.712 3 7728.059 3 0.0072 16.6 0.40 (17) −2.57 ± 0.07
251.7123 47092.712 3 7376.764 4 0.0321 7.3 1.77 (9) −1.93 ± 0.04
215.5020 47092.712 3 704.007 2 0.0157 25.2 0.86 (26) −2.38 ± 0.10
214.1718 47092.712 3 415.933 3 0.0212 15.3 1.16 (16) −2.25 ± 0.07
744.3022 47197.010 2 33765.304 2 0.0125 13.0 0.55 (14) −1.64 ± 0.06
437.3561 47197.010 2 24338.765 3 0.0230 6.7 1.01 (8) −1.84 ± 0.04 −1.83 ± 0.09 OB91 P
437.2987 47197.010 2 24335.764 2 0.0064 22.6 0.28 (23) −2.40 ± 0.09 −2.58 ± 0.18 MA74
412.2516 47197.010 2 22946.814 1 0.0710 5.7 3.10 (8) −1.40 ± 0.03 −1.39 ± 0.04 OB91 P
410.4154 47197.010 2 22838.321 2 0.0073 8.8 0.32 (10) −2.40 ± 0.04
382.1835 47197.010 2 21038.986 2 0.1889 4.7 8.25 (7) −1.044 ± 0.03 −1.10 ± 0.04 OB91 P
341.5531 47197.010 2 17927.381 1 0.0839 6.6 3.67 (8) −1.49 ± 0.04 −1.39 ± 0.05 OB91 P
339.2305 47197.010 2 17726.987 2 0.1783 5.8 7.79 (8) −1.17 ± 0.03 −1.07 ± 0.05 OB91 P
292.0691 47197.010 2 12968.553 2 0.1060 7.2 4.63 (9) −1.53 ± 0.04 −1.39 ± 0.04 OB91 P
288.6317 47197.010 2 12560.933 3 0.0335 10.8 1.47 (12) −2.039 ± 0.05 −2.09 ± 0.04 OB91 P
256.0557 47197.010 2 8154.713 1 0.0405 7.7 1.77 (9) −2.061 ± 0.04 −2.11 ± 0.04 OB91 P
254.9525 47197.010 2 7985.784 2 0.0081 21.3 0.35 (22) −2.77 ± 0.09 −2.49 ± 0.05 OB91 P
253.2876 47197.010 2 7728.059 3 0.0328 8.0 1.43 (10) −2.16 ± 0.04 −2.16 ± 0.04 OB91 P
215.0185 47197.010 2 704.007 2 0.0311 18.2 1.36 (19) −2.33 ± 0.08
393.5307 48350.606 1 22946.814 1 0.0102 16.0 0.91 (17) −2.199 ± 0.07 −1.82 ± 0.18 MA74
328.6016 48350.606 1 17927.381 1 0.0106 20.6 0.94 (21) −2.34 ± 0.08
326.4513 48350.606 1 17726.987 2 0.0261 15.2 2.33 (16) −1.95 ± 0.06 −1.32 ± 0.05 OB91 P
248.7066 48350.606 1 8154.713 1 0.6014 2.6 53.70 (6) −0.83 ± 0.02 −0.75 ± 0.05 OB91 P
247.6657 48350.606 1 7985.784 2 0.2956 4.9 26.39 (7) −1.14 ± 0.03 −1.08 ± 0.04 OB91 P
537.9574 48382.603 5 29798.934 4 0.0128 3.9 0.79 (6) −1.42 ± 0.03 −1.51 ± 0.04 OB91 P
524.2491 48382.603 5 29313.006 6 0.0526 2.7 3.25 (6) −0.83 ± 0.02 −0.97 ± 0.04 OB91 P
511.0358 48382.603 5 28819.952 5 0.0148 4.0 0.91 (6) −1.41 ± 0.03 −1.37 ± 0.04 OB91 P
459.5358 48382.603 5 26627.607 4 0.0087 5.0 0.54 (7) −1.73 ± 0.03 −1.76 ± 0.04 OB91 P
419.9095 48382.603 5 24574.653 4 0.8193 0.6 50.57 (5) 0.17 ± 0.02 0.16 ± 0.04 OB91 P
412.0206 48382.603 5 24118.817 4 0.0345 3.1 2.13 (6) −1.23 ± 0.03 −1.27 ± 0.04 OB91 P
378.9176 48382.603 5 21999.129 4 0.0317 4.1 1.96 (7) −1.33 ± 0.03 −1.29 ± 0.04 OB91 P
360.3681 48382.603 5 20641.109 4 0.0060 11.7 0.37 (13) −2.10 ± 0.05 −2.01 ± 0.08 OB91 P
347.5863 48382.603 5 19621.005 5 0.0115 18.4 0.71 (19) −1.85 ± 0.08
470.8969 50586.878 3 29356.742 2 0.0068 28.4 0.37 (29) −2.07 ± 0.11 −2.03 ± 0.09 OB91 P
454.7847 50586.878 3 28604.611 2 0.1279 2.1 6.91 (6) −0.82 ± 0.02 −1.01 ± 0.12 OB91 P
417.1900 50586.878 3 26623.733 2 0.0221 6.1 1.20 (8) −1.66 ± 0.03 −1.70 ± 0.05 OB91 P
410.3611 50586.878 3 26224.967 3 0.0022 18.8 0.12 (20) −2.67 ± 0.08
384.3257 50586.878 3 24574.653 4 0.7374 0.8 39.86 (5) −0.21 ± 0.02 −0.24 ± 0.04 OB91 P
380.8282 50586.878 3 24335.764 2 0.0177 16.3 0.95 (17) −1.84 ± 0.07 −1.94 ± 0.06 OB91 P
352.7891 50586.878 3 22249.428 3 0.0148 21.3 0.80 (22) −1.98 ± 0.09
302.6056 50586.878 3 17550.180 3 0.0161 26.2 0.87 (27) −2.077 ± 0.10
697.7429 51373.910 5 37045.932 4 0.0068 10.7 0.47 (12) −1.42 ± 0.05
540.3822 51373.910 5 32873.630 4 0.0319 3.1 2.20 (6) −0.98 ± 0.03 −1.03 ± 0.05 OB91 P
453.1636 51373.910 5 29313.006 6 0.0048 12.1 0.33 (13) −1.95 ± 0.05
443.2568 51373.910 5 28819.952 5 0.0117 12.0 0.80 (13) −1.58 ± 0.05 −1.56 ± 0.18 MA74
395.6455 51373.910 5 26105.906 6 0.2287 2.5 15.77 (6) −0.39 ± 0.02 −0.34 ± 0.04 OB91 P
373.0386 51373.910 5 24574.653 4 0.1296 4.9 8.94 (7) −0.69 ± 0.03 −0.65 ± 0.04 OB91 P
337.0783 51373.910 5 21715.731 5 0.3413 3.9 23.54 (6) −0.36 ± 0.03 −0.27 ± 0.04 OB91 P
325.2915 51373.910 5 20641.109 4 0.0267 9.8 1.84 (11) −1.49 ± 0.05 −1.42 ± 0.04 OB91 P
312.5683 51373.910 5 19390.167 6 0.1049 5.7 7.23 (8) −0.93 ± 0.03 −0.87 ± 0.04 OB91 P
253.7459 51373.910 5 11976.238 4 0.0604 9.6 4.17 (11) −1.35 ± 0.05 −1.47 ± 0.06 OB91 P
420.3938 53093.528 6 29313.006 6 0.0342 7.2 3.23 (9) −0.95 ± 0.04 −0.99 ± 0.04 OB91 P
411.8545 53093.528 6 28819.952 5 0.5906 3.2 55.72 (6) 0.27 ± 0.03 0.22 ± 0.04 OB91 P
373.8305 53093.528 6 26351.038 5 0.3624 5.2 34.18 (7) −0.031 ± 0.03 −0.03 ± 0.04 OB91 P

Notes.

aWavelengths, upper and lower energy levels and J quantum numbers are taken from Kramida et al. (2011). bThe measured branching fraction, BF, is expressed per unit and its relative uncertainty, δBF/BF, as a percentage. cThe measured transition probability, Aul, in 106 s−1. In brackets, its uncertainty expressed in percentage. dThe log $({gf})$ values measured in this work together with their uncertainty index. eValues of log $({gf}){\rm{s}}$ from other authors used for comparison with their uncertainty index. The acronyms in the reference column correspond to BL79—Blackwell et al. (1979a, 1979b), OB91—O'Brian et al. (1991), BL82a—Blackwell et al. (1982a), MA74—May et al. (1974), BL82b—Blackwell et al. (1982b), and BA94—Bard & Kock (1994). The letter included after the reference OB91 indicates the method used by the authors, with "L" and "P" standing for "lifetime" and "population" method, respectively.

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Figures 2 and 3 show the comparison between the new log $({gf})$ values obtained in this experiment and those published previously, indicating if they agree within one or two σ, which represents the combined experimental uncertainty. Both plots include dashed horizontal lines indicating uncertainties of ±25%, which correspond to values classified as "C" by Fuhr & Wiese (2006), regarding their accuracy. In Figure 2, our log $({gf}){\rm{s}}$ are compared with those from O'Brian et al. (1991). We made a distinction between the log $({gf}){\rm{s}}$ that were obtained from measurements of lifetimes and branching fractions and those determined from extrapolated energy level populations and relative line intensities. For 13 of the compared transitions, marked in Figure 2 by filled symbols, O'Brian et al. (1991) log $({gf}){\rm{s}}$ do not agree with our new values within 2σ. It is noted that only one of these values from O'Brian et al. (1991) was obtained from lifetime measurements, with the remaining 12 being determined by using the population method. Figure 3 shows the comparison with log $({gf})$ values from Blackwell et al. (1979a, 1979b, 1982a, 1982b), May et al. (1974), Bard & Kock (1994), and Banfield & Huber (1973). It is possible to see how log $({gf}){\rm{s}}$ from Blackwell et al. agree within 1σ with our new values, which is reassuring as their experiments are considered to be the most precise by Fuhr & Wiese (2006), with uncertainties lower than 2%. Relative log $({gf}){\rm{s}}$ from Blackwell et al. are claimed to be better than 2%. The comparison with log $({gf}){\rm{s}}$ from May et al. (1974), obtained from emission measurements from a wall-stabilized arc, shows a wider scatter, which is not strange given the large uncertainties assigned by Fuhr & Wiese (2006). The only log $({gf})$ value from Bard & Kock (1994) available for comparison shows a good agreement within 1σ, whereas the $\mathrm{log}({gf})$ from Banfield & Huber (1973) differs significantly from our value, although the difference lies within 2σ.

Figure 2.

Figure 2. Comparison of the new log $({gf})$ values measured in this work with those of O'Brian et al. (1991) obtained from lifetimes (L) and extrapolating energy level populations (P). The solid horizontal line represents perfect agreement between the two sets of values. The dashed horizontal line indicates uncertainties of ±25%, coded as "C" by Fuhr & Wiese (2006). Agreement within the combined experimental uncertainty is indicated by $\lt 1\sigma $.

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Figure 3.

Figure 3. Comparison between our new oscillator strengths and those from Blackwell et al. (1979a, 1979b, 1982a, 1982b), May et al. (1974), Bard & Kock (1994), and Banfield & Huber (1973). Close agreement with Blackwell et al. is used as an indication of the quality of our new data.

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4. Solar Spectral Synthesis

A subset of the new gf-values measured in this work were used to determine iron line abundances from the solar spectrum obtained with the Kitt Peak FTS by Kurucz et al. (1984). The high-quality observations and the well-known atmospheric parameters available for the Sun make it an ideal test case to evaluate the impact of new atomic data on stellar spectral synthesis. We selected 17 lines from Table 4 which show low contamination from blends at the spectral resolution of the solar flux atlas, and which are located in regions of good continuum placement. The observed spectrum has a minimum wavelength of 300 nm, and it is very crowded at wavelengths below ∼400 nm, which excludes about two-thirds of the lines published in this work. Among the remaining lines, about half were too blended to attempt any abundance derivation. The selected lines are listed in Table 5 together with the required input atomic data in columns 1–4 (central wavelength, lower level energy ${E}_{\mathrm{low}}$, gf-value, and van der Waals parameter). The latter is used to account for line broadening due to collisions with neutral hydrogen and was extracted from the VALD database (Kupka et al. 1999; Heiter et al. 2008). The meaning of the values for the van der Waals broadening parameter given in Table 5 (column 3) is as follows. Values greater than zero were obtained from Anstee, Barklem & O'Mara (ABO) theory (Anstee & O'Mara 1991, 1995; Barklem et al. 2000) and are expressed in a packed notation where the integer component is the broadening cross-section, σ, in atomic units, and the decimal component is the dimensionless velocity parameter, α. Values less than zero are the log of the broadening parameter, ${\gamma }_{6}$ (rad s−1), per unit perturber number density, N (cm−3), at 10,000 K (i.e., log[${\gamma }_{6}/N]$ in units of rad s−1 cm3) from Kurucz (2014). These were used only when ABO data were unavailable. See Gray (2005) for more details.

Table 5.  Lines from Table 4 Selected for Solar Synthesis

${\lambda }_{\mathrm{air}}$ ${E}_{\mathrm{low}}$ VdWa This Experiment Previously Published ${v}_{\mathrm{macro}}$ New gf Previous gf
(nm) (eV) Parameter log(gf) Unc. log(gf) Unc.b Ref.c (km s−1) log(ε) rmsd log(ε) rmsd
380.8729 2.559 265.262 −1.17 0.04 −1.16 0.00 BL82b 3.2 7.47 0.9 7.46 0.9
412.0206 2.990 338.253 −1.23 0.03 −1.27 0.04 OB91 3.6 7.56 1.9 7.60 2.0
443.2568 3.573 275.254 −1.58 0.05 −1.56 0.18 MA74 3.2 7.39 1.0 7.38 1.0
444.7717 2.223 429.302 −1.36 0.03 −1.34 0.01 BL82a 3.2 7.60 0.6 7.58 0.7
445.9117 2.176 417.302 −1.29 0.03 −1.28 0.01 BL82a 2.5 7.50 0.9 7.49 0.9
449.4563 2.198 416.302 −1.14 0.03 −1.14 0.01 BL82a 3.1 7.46 1.2 7.46 1.2
451.4184 3.047 296.271 −1.96 0.05 −1.92 0.18 MA74 3.2 7.40 1.1 7.36 1.2
454.7847 3.546 313.266 −0.82 0.02 −1.01 0.12 OB91 3.1 7.41 1.5 7.59 1.6
459.5358 3.301 286.270 −1.73 0.03 −1.76 0.04 OB91 3.4 7.60 1.2 7.62 1.2
463.0120 2.279 416.254 −2.58 0.05 −2.59 0.12 OB91 3.0 7.56 1.7 7.56 1.7
470.8969 3.640 −7.800 −2.07 0.11 −2.03 0.09 OB91 4.1 7.92 0.7 7.88 0.7
537.9574 3.695 363.249 −1.42 0.03 −1.51 0.04 OB91 3.2 7.43 0.9 7.53 0.9
540.3822 4.076 −7.810 −0.98 0.03 −1.03 0.05 OB91 3.7 7.62 1.1 7.66 1.1
553.2747 3.573 237.255 −1.89 0.06 −2.10 0.30 MA74 3.4 7.25 0.4 7.45 0.4
721.9682 4.076 −7.740 −1.43 0.04 −1.73 K14 3.1 7.40 0.5 7.70 0.5
730.7931 4.143 −7.810 −1.15 0.03 −1.53 0.06 OB91 3.4 7.33 0.4 7.69 0.5
744.3022 4.186 −7.810 −1.64 0.06 −1.40 K14 3.4 7.47 0.5 7.24 0.5

Notes.

aVan der Waals broadening parameter (see the text for an explanation). bUncertainties are only available for experimentally measured log(gf) values. cReference acronyms are the same as for Table 4. In addition, K14 stands for Kurucz (2014). drms difference between observed and synthetic flux in percent, for the points included in the fit.

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The spectral synthesis was done with the one-dimensional, plane-parallel radiative transfer code SME (Valenti & Piskunov 1996; Piskunov & Valenti 2017, version 531), assuming LTE and using a model atmosphere interpolated in the MARCS grid included in the SME distribution (Gustafsson et al. 2008). We adopted an effective temperature of 5772 K and a logarithmic surface gravity (cm s−2) of 4.44 (Heiter et al. 2015a; Pršat et al. 2016), a microturbulence of 1.0 km s−1, and a projected rotational velocity of ${v}_{\mathrm{rot}}$ sin(i) = 1.6 km s−1 (Valenti & Piskunov 1996). The instrumental profile was assumed to be Gaussian, with a width corresponding to the spectral resolution of the observations (R = 200,000). Each line profile was fitted individually using ${\chi }^{2}$-minimization between observed and synthetic spectra while varying the iron abundance and the macroturbulence broadening, parameterized by a velocity ${v}_{\mathrm{macro}}$ in the radial-tangential model (Gray 2005). In addition, a small radial velocity correction was applied to each line, allowing for variations in the wavelength scale of the observations. For each line, we determined the region of the line profile which seemed to be free from blends in the observed spectrum, and only spectrum points within that region were used to calculate the ${\chi }^{2}$.

The results are given in Table 5, where we list the best-fit iron abundance log(ε) for each line (column 10) on the standard astronomical scale.4 We also list the ${v}_{\mathrm{macro}}$ values derived for each line (column 9), as well as a measure for the goodness of fit (rms deviation, column 11), ranging from 0.4% to 1.9%. The largest deviations are found for lines at wavelengths at or below 450 nm, and the smallest rms values for lines above 700 nm. Most of the abundances fall within the range from 7.3 to 7.6, with associated macroturbulence values between 2.5 and 3.7 km s−1 and radial velocity corrections of 0.2 to 0.4 km s−1. However, the line at 470.9 nm has ${v}_{\mathrm{macro}}\gtrsim 4$ and an abundance of 7.9, significantly higher than the above range. This indicates contamination by undetected blends that have not been taken into account in the fit. Excluding this line, the mean abundance and standard deviation are log ${(\varepsilon )}_{\mathrm{new}}$ = 7.47 ± 0.10 dex5 (16 lines), which is similar to the values found in the previous two papers in this series (7.44 ± 0.08 dex in Ruffoni et al. 2014 and 7.45 ± 0.06 dex in Den Hartog et al. 2014), and agrees with recent publications, such as 7.43 ± 0.05 from Bergemann et al. (2012) (MARCS LTE result), and 7.40 ± 0.04 from Scott et al. (2015) (mean of MARCS LTE abundances in their Table 1).

The line-to-line abundance scatter might be influenced by non-LTE effects, which are however expected to be small in solar-like atmospheres. Unfortunately non-LTE corrections have only been published for few of the lines analyzed here. Four of the lines were investigated by Gehren et al. (2001), who derived non-LTE−LTE abundance differences of 0.03 dex for the 449.5 and 538.0 nm lines, 0.05 dex for 444.8 nm, and −0.11 dex for 443.3 nm. Applying these corrections would lead to a slightly larger scatter. On the other hand, the more recent calculations by Bergemann et al. (2012) and Lind et al. (2012), made available through the INSPECT database,6 include two of the lines (449.5, 538.0 nm), both with non-LTE corrections of 0.01 dex. If similar corrections apply to the remaining lines then they do not have any impact on the abundance scatter derived here.

We repeated the abundance determination for the same set of lines using the best previously published experimental or theoretical log(gf) values (see Table 5 for values and references in columns 6–8, and for results in columns 12 and 13). The regions of the line profiles used for the fit were the same as above, and the macroturbulence values were those derived in the analysis with the new log(gf) values7 The results for both the previously published data and the new data are illustrated in Figure 4. The differences in derived abundances are consistent with the differences in log(gf), and are larger than 0.05 dex for six lines.8 The mean abundance and standard deviation for previous data including the same 16 lines as above are log ${(\varepsilon )}_{\mathrm{pub}}=7.52\pm 0.13$ dex, which is close to log ${(\varepsilon )}_{\mathrm{new}}$, although slightly offset toward higher abundances and with a somewhat larger scatter. In summary, the small scatter in the line abundances derived with the new data, and the satisfactory agreement with recently published values for the solar iron abundance validates the general accuracy of the new measurements.

Figure 4.

Figure 4. Solar iron abundance, log(ε), obtained from the synthesis of individual lines listed in Table 5 using the log(gf) values from this work, log ${({gf})}_{\mathrm{new}}$ (lower panel), and the best previously published values, log ${({gf})}_{\mathrm{pub}}$ (upper panel). The point in each panel marked with a cross may be affected by undetected blends (see the text) and was excluded from the calculation of the average log $(\varepsilon )$. The solid and dotted horizontal lines in each panel indicate the unweighted average abundance and the standard deviation, respectively. The error bars indicate only the uncertainty of the experimental gf-values (columns 5 and 7 in Table 5) and do not capture the uncertainties associated with the solar atmospheric modeling and spectral synthesis.

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5. Conclusions

We report radiative lifetimes for 60 odd-parity energy levels ranging from 27,166 to 57,562 cm−1, 39 of which have not been measured before. The uncertainties for these lifetimes are the larger of ±5% or 0.2 ns. When values are available in the literature, our results are in good agreement with them.

We provide 120 experimental log $({gf})$ values (transition probabilities) for Fe i transitions within the spectral range 213–1033 nm coming from 16 upper energy levels, 24 of which had no previous experimental data. The uncertainty of these oscillator strengths has been carefully calculated and it ranges between 0.02 dex for the strongest lines and 0.09 dex for the very weak ones. This accuracy is an improvement over previous log $({gf})$ measurements for around 72 of the transitions, making our new log $({gf})$ values good candidates for use in the analysis of stellar spectra and the determination of chemical abundances. Our log $({gf})$ results are in good agreement with those of Blackwell et al. (1979a, 1979b, 1982a, 1982b) and in general with O'Brian et al. (1991) data.

M.T.B., J.C.P., and M.P.R. thank the UK Science and Technology Facilities Council (STFC) for support under research grant ST/N000838/1. E.A.D.H., J.E.L., and A.G. acknowledge funding from the National Science Foundation through award AST-1211055 and through the NSF REU program award AST-0907732. U.H. acknowledges support from the Swedish National Space Board (SNSB/Rymdstyrelsen). This work has made use of the VALD database, operated at Uppsala University, the Institute of Astronomy RAS in Moscow, and the University of Vienna. This work has made use of the NSO/Kitt Peak FTS data, produced by NSF/NOAO.

Footnotes

  • ${\mathrm{log}}_{10}(\varepsilon )={\mathrm{log}}_{10}({N}_{\mathrm{Fe}}/{N}_{{\rm{H}}})$ + 12, where ${N}_{\mathrm{Fe}}$ and ${N}_{{\rm{H}}}$ are the number densities of iron and hydrogen atoms, respectively.

  • The unit dex stands for decimal exponent, x dex = 10x.

  • Simultaneous variation of macroturbulence resulted in the same ${v}_{\mathrm{macro}}$ values, except for two lines: 553.3 nm and 730.8 nm, with 7% and 9% lower values, respectively.

  • 454.8, 538.0, 553.3, 722.0, 730.8, 744.3 nm.

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10.3847/1538-4357/aa8cd3