纤锌矿晶体结构
化学物理
结晶学
相(物质)
钙钛矿(结构)
材料科学
离子
化学
单独一对
纳米技术
扩散
分子
热力学
物理
有机化学
六方晶系
作者
Eric A. Gabilondo,Shaun O’Donnell,Ryan Newell,Rachel Broughton,Marcelo Mateus,Jacob L. Jones,Paul A. Maggard
标识
DOI:10.1002/chem.202200479
摘要
Abstract Recently, many new, complex, functional oxides have been discovered with the surprising use of topotactic ion‐exchange reactions on close‐packed structures, such as found for wurtzite, rutile, perovskite, and other structure types. Despite a lack of apparent cation‐diffusion pathways in these structure types, synthetic low‐temperature transformations are possible with the interdiffusion and exchange of functional cations possessing n s 2 stereoactive lone pairs (e. g., Sn(II)) or unpaired n d x electrons (e. g., Co(II)), targeting new and favorable modulations of their electronic, magnetic, or catalytic properties. This enables a synergistic blending of new functionality to an underlying three‐dimensional connectivity, i. e., [‐M−O‐M‐O‐] n , that is maintained during the transformation. In many cases, this tactic represents the only known pathway to prepare thermodynamically unstable solids that otherwise would commonly decompose by phase segregation, such as that recently applied to the discovery of many new small bandgap semiconductors.
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