{"title":"软晶格无机固体中的高原-雷利不稳定性","authors":"Zhen-Chao Shao, Xianyun Jiang, Chong Zhang, Tianhao Wang, Yan-Ru Wang, Guo-Qiang Liu, Zong-Ying Huang, Yu-Zhuo Zhang, Liang Wu, Zhong-Huai Hou, Huijun Jiang, Yi Li, Shu-Hong Yu","doi":"10.1021/jacs.4c11866","DOIUrl":null,"url":null,"abstract":"Plateau–Rayleigh instability─a macroscopic phenomenon describing the volume-constant breakup of one-dimensional continuous fluids─has now been widely observed in adatoms, liquids, polymers, and liquid metals. This instability enables controlled wetting–dewetting behavior at fluid–solid interfaces and, thereby, the self-limited patterning into ordered structures. However, it has yet to be observed in conventional inorganic solids, as the rigid lattices restrict their “fluidity”. Here, we report the general fluid-like Plateau–Rayleigh instability of silver-based chalcogenide semiconductors featuring soft-lattice ionic crystals. It enables postsynthetic morphing from conformal core–shell nanowires to periodically coaxial ones. We reveal that such self-limited reconstruction is thermodynamically driven by the surface energy and interface energy and kinetically favored by the high ionic diffusion coefficients of subnanoscale soft-lattice shells. The resulting periodic heterostructures can be topotactically transformed for epitaxial combinations of functional semiconductors free from the lattice-matching rule. This fluid-like behavior in soft inorganic solids thus offers routes toward sophisticated nanostructures and controllable patterning at all-inorganic solid–solid interfaces.","PeriodicalId":49,"journal":{"name":"Journal of the American Chemical Society","volume":"254 1","pages":""},"PeriodicalIF":14.4000,"publicationDate":"2024-11-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Plateau–Rayleigh Instability in Soft-Lattice Inorganic Solids\",\"authors\":\"Zhen-Chao Shao, Xianyun Jiang, Chong Zhang, Tianhao Wang, Yan-Ru Wang, Guo-Qiang Liu, Zong-Ying Huang, Yu-Zhuo Zhang, Liang Wu, Zhong-Huai Hou, Huijun Jiang, Yi Li, Shu-Hong Yu\",\"doi\":\"10.1021/jacs.4c11866\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Plateau–Rayleigh instability─a macroscopic phenomenon describing the volume-constant breakup of one-dimensional continuous fluids─has now been widely observed in adatoms, liquids, polymers, and liquid metals. This instability enables controlled wetting–dewetting behavior at fluid–solid interfaces and, thereby, the self-limited patterning into ordered structures. However, it has yet to be observed in conventional inorganic solids, as the rigid lattices restrict their “fluidity”. Here, we report the general fluid-like Plateau–Rayleigh instability of silver-based chalcogenide semiconductors featuring soft-lattice ionic crystals. It enables postsynthetic morphing from conformal core–shell nanowires to periodically coaxial ones. We reveal that such self-limited reconstruction is thermodynamically driven by the surface energy and interface energy and kinetically favored by the high ionic diffusion coefficients of subnanoscale soft-lattice shells. The resulting periodic heterostructures can be topotactically transformed for epitaxial combinations of functional semiconductors free from the lattice-matching rule. This fluid-like behavior in soft inorganic solids thus offers routes toward sophisticated nanostructures and controllable patterning at all-inorganic solid–solid interfaces.\",\"PeriodicalId\":49,\"journal\":{\"name\":\"Journal of the American Chemical Society\",\"volume\":\"254 1\",\"pages\":\"\"},\"PeriodicalIF\":14.4000,\"publicationDate\":\"2024-11-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of the American Chemical Society\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1021/jacs.4c11866\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the American Chemical Society","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/jacs.4c11866","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Plateau–Rayleigh Instability in Soft-Lattice Inorganic Solids
Plateau–Rayleigh instability─a macroscopic phenomenon describing the volume-constant breakup of one-dimensional continuous fluids─has now been widely observed in adatoms, liquids, polymers, and liquid metals. This instability enables controlled wetting–dewetting behavior at fluid–solid interfaces and, thereby, the self-limited patterning into ordered structures. However, it has yet to be observed in conventional inorganic solids, as the rigid lattices restrict their “fluidity”. Here, we report the general fluid-like Plateau–Rayleigh instability of silver-based chalcogenide semiconductors featuring soft-lattice ionic crystals. It enables postsynthetic morphing from conformal core–shell nanowires to periodically coaxial ones. We reveal that such self-limited reconstruction is thermodynamically driven by the surface energy and interface energy and kinetically favored by the high ionic diffusion coefficients of subnanoscale soft-lattice shells. The resulting periodic heterostructures can be topotactically transformed for epitaxial combinations of functional semiconductors free from the lattice-matching rule. This fluid-like behavior in soft inorganic solids thus offers routes toward sophisticated nanostructures and controllable patterning at all-inorganic solid–solid interfaces.
期刊介绍:
The flagship journal of the American Chemical Society, known as the Journal of the American Chemical Society (JACS), has been a prestigious publication since its establishment in 1879. It holds a preeminent position in the field of chemistry and related interdisciplinary sciences. JACS is committed to disseminating cutting-edge research papers, covering a wide range of topics, and encompasses approximately 19,000 pages of Articles, Communications, and Perspectives annually. With a weekly publication frequency, JACS plays a vital role in advancing the field of chemistry by providing essential research.