2011
DOI: 10.1366/10-06015
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Quantification of Iron (Fe) in Lithium Niobate by Optical Absorption

Abstract: A quantitative method, based solely on optical absorption, to determine the total iron (Fe) concentration in Fe : LiNbO3 is proposed. Absorption spectra of several samples doped by thermal diffusion with different concentrations and different [Fe2+]/[Fe3+] ratios show an isosbestic point at 342 nm. At this wavelength the absorption is proportional to the total Fe concentration and does not depend on the oxidation state. Thanks to the large number of samples covering a wide range of concentrations, in this work… Show more

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Cited by 24 publications
(20 citation statements)
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“…This fosters the optical excitation via the iron C-band, though an excitation via the D-band cannot be excluded. We additionally need to consider that the cross-sections of these two excitation paths are very similar at 355 nm [27], i.e, a contribution of both paths to the transient spectrum is to be expected. In this sense, and in direct comparison with the discussion of the previous section, it is likely to assume that the observed NIR absorption feature with fast decay in the spectra of Fig.…”
Section: Excitation Via the Iron D-band + C-bandmentioning
confidence: 99%
“…This fosters the optical excitation via the iron C-band, though an excitation via the D-band cannot be excluded. We additionally need to consider that the cross-sections of these two excitation paths are very similar at 355 nm [27], i.e, a contribution of both paths to the transient spectrum is to be expected. In this sense, and in direct comparison with the discussion of the previous section, it is likely to assume that the observed NIR absorption feature with fast decay in the spectra of Fig.…”
Section: Excitation Via the Iron D-band + C-bandmentioning
confidence: 99%
“…The sample with the highest doping level was chemically reduced under a mixture of Ar − H 2 atmosphere at 500 K for several hours. The absorption coefficient at 532 nm was measured for samples Fe:LN 0.02 mol % and Fe:LN 0.05 mol %, from which the Fe 2+ concentration was obtained [20]. For sample Fe:LN 0.1 mol %, instead, due to the high absorption level, we preferred to use the datum at 1128 nm [21] from which the Fe 2+ concentration was also deduced.…”
Section: Samplesmentioning
confidence: 99%
“…Quite surprisingly, there exist few experimental and theoretical studies reporting on the direct investigation of the most basic characteristics of the Fe bound polaron, i.e., the local distortion produced by the self-trapping action and its electronic structure. Generally, the incorporation of Fe in LNB was experimentally studied only from the point of view of lattice site location and determination of the Fe valence state [14][15][16][17][18][19][20][21][22][23][24]. However, some recent XRD results [25] showed that the electron capture by the Fe center produces a strain in the crystal matrix, indicating the onset of a measurable deformation at the Fe centers when their valence is changed from Fe 3+ to Fe 2+ by a reduction treatment.…”
Section: Introductionmentioning
confidence: 99%