Photoinduced transformations in (As1–xBix)2S3 glass observed by Raman spectroscopy

IF 2.4 3区 化学 Q2 SPECTROSCOPY Journal of Raman Spectroscopy Pub Date : 2024-02-06 DOI:10.1002/jrs.6658
Yuriy Azhniuk, Vasyl Lopushansky, Stepan Hasynets, Volodymyr Kryshenik, Alexander V. Gomonnai, Dietrich R. T. Zahn
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Abstract

Raman spectra of (As1–xBix)2S3 glass samples with x ≤ 0.2 measured at the excitation with above-bandgap (532 nm) laser light at a relatively low power density (Pexc = 4 kW/cm2) clearly confirm the amorphous character, thereby markedly extending the known compositional interval of existence of the (As1–xBix)2S3 glass previously known (x ≤ 0.06). Spectra measured at an increased Pexc (40 kW/cm2) reveal a photostructural transformation in the illuminated area of the glass leading to an additional contribution of Bi–S bonds as well as to an increasing number of cage-type As4S4 units with homopolar As–As bonds. A number of new features in a broad range up to about 1,000 cm−1, which emerge in the Raman spectra of the (As1–xBix)2S3 glasses with high (x ≥ 0.14) Bi content and increase in intensity with the exposure time, are related to a photochemical transformation, namely, oxidation of arsenic and sulphur on the (As1–xBix)2S3 glass surface with formation of units containing arsenate AsO43− and sulphate SO42− ions. These processes are irreversible and occur only in the presence of a sufficient amount of bismuth.

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拉曼光谱观察(As1-xBix)2S3 玻璃中的光诱导转变
在相对较低的功率密度(Pexc = 4 kW/cm2)下,用高于带隙(532 nm)的激光激发时测量的 x ≤ 0.2 的 (As1-xBix)2S3 玻璃样品的拉曼光谱清楚地证实了其非晶体特性,从而明显扩大了之前已知的 (As1-xBix)2S3 玻璃(x ≤ 0.06)的存在成分范围。在更高的 Pexc(40 kW/cm2)条件下测量到的光谱显示,玻璃光照区域的光结构发生了转变,导致 Bi-S 键的额外贡献以及具有同极性 As-As 键的笼型 As4S4 单元数量的增加。在(As1-xBix)2S3玻璃的拉曼光谱中,出现了一些新的特征,范围宽达约 1,000 cm-1,这些特征的Bi含量高(x ≥ 0.14),强度随照射时间的延长而增加,它们与光化学转变有关,即(As1-xBix)2S3玻璃表面的砷和硫被氧化,形成含有砷酸根 AsO43- 和硫酸根 SO42- 离子的单元。这些过程是不可逆的,只有在有足够量的铋存在时才会发生。
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来源期刊
CiteScore
5.40
自引率
8.00%
发文量
185
审稿时长
3.0 months
期刊介绍: The Journal of Raman Spectroscopy is an international journal dedicated to the publication of original research at the cutting edge of all areas of science and technology related to Raman spectroscopy. The journal seeks to be the central forum for documenting the evolution of the broadly-defined field of Raman spectroscopy that includes an increasing number of rapidly developing techniques and an ever-widening array of interdisciplinary applications. Such topics include time-resolved, coherent and non-linear Raman spectroscopies, nanostructure-based surface-enhanced and tip-enhanced Raman spectroscopies of molecules, resonance Raman to investigate the structure-function relationships and dynamics of biological molecules, linear and nonlinear Raman imaging and microscopy, biomedical applications of Raman, theoretical formalism and advances in quantum computational methodology of all forms of Raman scattering, Raman spectroscopy in archaeology and art, advances in remote Raman sensing and industrial applications, and Raman optical activity of all classes of chiral molecules.
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