Microwave-assisted intercalation: exploring electronic and structural features of metastable MMo6S8 (M = Ag, Sn)†

IF 5.2 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY
Rose E. Smiley, Konstantina G. Mason, Rose A. Lam, Alice Giem, Daniella Ingargiola, Brian A. Wuille Bille, David Prendergast and Jesús M. Velázquez
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引用次数: 0

Abstract

Presented in this work is a synthetic approach for metastable Type I Chevrel phase sulfides, MMo6S8 (M = Ag, Sn), utilizing rapid microwave-assisted medium temperature intercalation. Using X-ray absorption spectroscopy the electronic structure and local coordination of sulfur and molybdenum bonding environments are probed as a function of a Type I metal intercalant. Intercalant promoter-induced electron donation effects were observed through analysis of the sulfur K-edge pre-edge feature and Mo L3-edge in the X-ray absorption near edge regions. Calculated electron density maps reveal more covalent interactions between Ag and S atoms versus more ionic interactions between Sn and S. Changes in the Chevrel phase structure upon intercalation are investigated through Mo K-edge extended X-ray absorption fine structure analysis. Evaluation of Mo–Mo intracluster distances allows the cluster anisotropy of Type I CPs to be calculated as low as 1.84%. These findings help elucidate how electronic and local structures can be modulated through intercalation and the importance of cation identity to fine tune structures.

Abstract Image

微波辅助插层:探讨亚稳MMo6S8 (M = Ag, Sn)†的电子和结构特征
本文提出了一种利用快速微波辅助中温插层合成亚稳I型Chevrel相硫化物MMo6S8 (M = Ag, Sn)的方法。利用x射线吸收光谱研究了硫和钼键合环境的电子结构和局部配位作为I型金属插层剂的函数。通过对x射线吸收近边区硫k边前边特征和钼l3边特征的分析,观察了嵌入剂启动子诱导的电子给能效应。计算得到的电子密度图显示Ag和S原子之间的共价相互作用更多,而Sn和S原子之间的离子相互作用更多。通过Mo k边扩展x射线吸收精细结构分析研究了嵌入后的Chevrel相结构的变化。通过对Mo-Mo簇内距离的评估,可以计算出I型CPs的簇各向异性低至1.84%。这些发现有助于阐明电子和局部结构如何通过插层调制,以及阳离子身份对微调结构的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Materials Advances
Materials Advances MATERIALS SCIENCE, MULTIDISCIPLINARY-
CiteScore
7.60
自引率
2.00%
发文量
665
审稿时长
5 weeks
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