纳米材料
纳米技术
纳米结构
材料科学
限制
纳米晶
离子
桥接(联网)
金属
化学
水溶液中的金属离子
纳米颗粒
兴奋剂
作者
Miri Kim,Min Ji Kim,Yizhi Zhang,Wonsik Jang,Jiho Yeom,Jongkyoung Kim,Hyo-Seok Kim,Seung-Hyun Lee,Jin-Ho Lee,Sanjay Mathur,Haiyan Wang,Junghwan Kim,Sukbin Lee,Seungho Cho
出处
期刊:Nano Letters
[American Chemical Society]
日期:2025-11-21
标识
DOI:10.1021/acs.nanolett.5c05165
摘要
Multielement nanostructures promise unusual properties but are constrained by crystalline frameworks limiting incorporable cations, and prevailing syntheses rely on harsh conditions restricting practicality. Here we introduce a CO2-enabled, room-temperature route to nanostructures containing up to 30 different metal cations by coengineering cation and anion arrangements in layered-double-hydroxide-derived frameworks. The key principle is anion-cation arrangement control: CO2-derived carbonate acts as a programmable bridging anion that, with larger-radius and higher-valent cations, drives structural reconstruction, suppresses long-range order, and relaxes radius-ratio constraints. This reorganization yields uniform cation mixing, tunable M3+/M2+ balance, and direct metal-carbonate linkages, producing ultrahigh configurational and positional disorder. The synthesis proceeds under ambient conditions in carbonated water, enabling compositional tunability, equimolar incorporation across 30 elements, and scalable, ecofriendly processing that valorizes a greenhouse gas. Leveraging anion-cation coarrangement to expand the composition space offers a general strategy for designing multielement nanomaterials with enhanced functional freedom.
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