材料科学
共晶体系
相变
范德瓦尔斯力
凝聚态物理
异质结
电介质
相(物质)
化学物理
晶体结构
铁电性
格子(音乐)
纳米技术
结晶学
光电子学
化学
微观结构
物理
有机化学
分子
声学
冶金
作者
Michael A. Susner,Marius Chyasnavichyus,Alexander A. Puretzky,Qian He,Benjamin S. Conner,Yang Ren,David A. Cullen,Panchapakesan Ganesh,Dongwon Shin,Hakan Demir,Jake Mcmurray,Albina Y. Borisevich,Petro Maksymovych,Michael A. McGuire
出处
期刊:ACS Nano
[American Chemical Society]
日期:2017-07-07
卷期号:11 (7): 7060-7073
被引量:64
标识
DOI:10.1021/acsnano.7b02695
摘要
Single crystals of the van der Waals layered ferrielectric material CuInP2S6 spontaneously phase separate when synthesized with Cu deficiency. Here we identify a route to form and tune intralayer heterostructures between the corresponding ferrielectric (CuInP2S6) and paraelectric (In4/3P2S6) phases through control of chemical phase separation. We conclusively demonstrate that Cu-deficient Cu1-xIn1+x/3P2S6 forms a single phase at high temperature. We also identify the mechanism by which the phase separation proceeds upon cooling. Above 500 K both Cu+ and In3+ become mobile, while P2S64- anions maintain their structure. We therefore propose that this transition can be understood as eutectic melting on the cation sublattice. Such a model suggests that the transition temperature for the melting process is relatively low because it requires only a partial reorganization of the crystal lattice. As a result, varying the cooling rate through the phase transition controls the lateral extent of chemical domains over several decades in size. At the fastest cooling rate, the dimensional confinement of the ferrielectric CuInP2S6 phase to nanoscale dimensions suppresses ferrielectric ordering due to the intrinsic ferroelectric size effect. Intralayer heterostructures can be formed, destroyed, and re-formed by thermal cycling, thus enabling the possibility of finely tuned ferroic structures that can potentially be optimized for specific device architectures.
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