What Can Chemical Bonding Tell Us about Photoinduced Phase Transition Reactions in Inorganic Semiconductors? Insight from Bismuth–Antimony Selenide

IF 4.3 2区 化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR Inorganic Chemistry Pub Date : 2024-11-11 DOI:10.1021/acs.inorgchem.4c03454
Anchal Vashishtha, Subila Kurukkal Balakrishnan, Yaniv Dror, Jitendra Kumar, Priyakumari Chakkingal Parambil, Eran Edri
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Abstract

Photoreactive self-healing semiconductors with suitable bandgaps for solar energy conversion offer an intriguing path to making resilient and low-cost photovoltaic devices through the introduction of a self-recovery path. However, only a few inorganic photovoltaic materials have such quality, and the underlying chemical properties that enable it are unknown, which poses a significant limit to our ability to study and discover new self-healing semiconductors. Recently, we have found that antimony trichalcogenide (Sb2Se3 and Sb2S3) and chalcohalides (e.g., SbSeI) can undergo a reversible photoinduced phase transition (PIPT) in which the structure is restored after photoinduced damage incurs to the materials. This group of materials offer a unique opportunity for studying PIPT and its limits. In particular, this group of materials facilitate the study of functional permutation to specific crystalline sites and to finding the limits of PIPT occurrence, which sheds light on the origin of the PIPT and self-recovery of this class of materials. Using Raman spectroscopy of thin films, and following signature vibrations of transition species, we have found that the PIPT magnitude decays upon gradual BiSb(1) substitution in a Sb2–xBixSe3 homologous series, until nearly one in five Sb ions is substituted with Bi. Then, the PIPT diminishes completely. The homologous series occurs along a transition from covalent to metavalent chemical bonding. By expanding our search, we find that a correlation between bonding type and photoreactivity does exist but conclude that it is an insufficient condition. Instead, we suggest, based on bond order and additional DFT calculations, that sufficient bonding states at the bottom of the conduction band are also required. This joint experimental and computational study pushes the limits of designing self-healing inorganic semiconductors for various applications and provides tools for further expansion.

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化学键对无机半导体光诱导相变反应有何启示?硒化铋锑的启示
光活性自愈合半导体具有适合太阳能转换的带隙,通过引入自恢复路径,为制造弹性好、成本低的光伏设备提供了一条引人入胜的道路。然而,只有少数无机光伏材料具有这样的品质,而且实现这种品质的基本化学特性尚不清楚,这极大地限制了我们研究和发现新型自修复半导体的能力。最近,我们发现三卤化锑(Sb2Se3 和 Sb2S3)和卤化物(如 SbSeI)可以发生可逆的光诱导相变(PIPT),在材料受到光诱导损伤后,其结构会得到恢复。这组材料为研究 PIPT 及其限制提供了独特的机会。特别是,这组材料有助于研究特定结晶位点的功能排列,并找到 PIPT 发生的极限,从而揭示 PIPT 的起源和这一类材料的自我恢复。利用薄膜的拉曼光谱和过渡物种的特征振动,我们发现在 Sb2-xBixSe3 同源系列中,当 BiSb(1) 逐渐被取代时,PIPT 的大小会逐渐减小,直到将近五分之一的 Sb 离子被 Bi 取代。然后,PIPT 完全减小。该同源系列是沿着从共价化学键到偏价化学键的过渡而出现的。通过扩大搜索范围,我们发现键合类型与光反应之间确实存在相关性,但得出的结论是,这是一个不充分的条件。相反,根据键序和额外的 DFT 计算,我们认为导带底部也需要足够的键合状态。这项实验和计算联合研究突破了为各种应用设计自修复无机半导体的极限,并为进一步扩展提供了工具。
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来源期刊
Inorganic Chemistry
Inorganic Chemistry 化学-无机化学与核化学
CiteScore
7.60
自引率
13.00%
发文量
1960
审稿时长
1.9 months
期刊介绍: Inorganic Chemistry publishes fundamental studies in all phases of inorganic chemistry. Coverage includes experimental and theoretical reports on quantitative studies of structure and thermodynamics, kinetics, mechanisms of inorganic reactions, bioinorganic chemistry, and relevant aspects of organometallic chemistry, solid-state phenomena, and chemical bonding theory. Emphasis is placed on the synthesis, structure, thermodynamics, reactivity, spectroscopy, and bonding properties of significant new and known compounds.
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