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Direct Observation of Pressure-Driven Valence Electron Transfer in Ba3BiRu2O9, Ba3BiIr2O9, and Ba4BiIr3O12

机译:在Ba3BiRu2O9,Ba3BiIr2O9和Ba4BiIr3O12中压力驱动价电子转移的直接观察

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摘要

The hexagonal perovskites Ba3BiIr2O9, Ba3BiRu2O9, and Ba4BiIr3O12 all undergo pressure-induced 1% volume collapses above 5 GPa. These first-order transitions have been ascribed to internal transfer of valence electrons between bismuth and iridium/ruthenium, which is driven by external applied pressure because the reduction in volume achieved by emptying the 6s shell of bismuth upon oxidation to Bi5+ is greater in magnitude than the increase in volume by reducing iridium or ruthenium. Here, we report direct observation of these valence transfers for the first time, using high-pressure X-ray absorption near-edge spectroscopy (XANES) measurements. Our data also support the highly unusual "4+" nominal oxidation state of bismuth in these compounds, although the possibility of local disproportionation into Bi3+/Bi5+ cannot be definitively ruled out. Ab initio calculations reproduce the transition, support its interpretation as a valence electron transfer from Bi to Ir/Ru, and suggest that the high-pressure phase may show metallic behavior (in contrast to the insulating ambient-pressure phase).
机译:六角形钙钛矿Ba3BiIr2O9,Ba3BiRu2O9和Ba4BiIr3O12均在5 GPa以上经历压力诱导的1%体积塌陷。这些一阶跃迁归因于价电子在铋和铱/钌之间的内部转移,这是由外部施加压力驱动的,因为在氧化成Bi5 +后排空铋的6s壳所实现的体积减小幅度大于通过减少铱或钌来增加体积。在这里,我们首次使用高压X射线吸收近边缘光谱(XANES)测量报告了这些价态转移的直接观察。我们的数据也支持这些化合物中铋的极不寻常的“ 4+”名义氧化态,尽管不能确切排除Bi3 + / Bi5 +局部歧化的可能性。从头算计算可以重现这种转变,支持将其解释为价电子从Bi转移到Ir / Ru,并暗示高压相可能显示出金属行为(与绝缘环境压力相相反)。

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