材料科学
纳米材料
结晶
纳米颗粒
铜
纳米尺度
化学工程
密度泛函理论
相(物质)
透射电子显微镜
金属
纳米技术
原位
氯化铜
电子衍射
氯化物
无机化学
转化(遗传学)
化学稳定性
表征(材料科学)
作者
Hyeuk Jin Han,Moon Young Yang,Changsoo Lee,Gangtae Jin,James L Hart,Rabecca Mutheu,Hyung-il Lee,Seo-Hyun Kim,Hanhwi Jang,Minjoon Kim,Yeon Sik Jung,William A. Goddard,Judy J. Cha,Chung-Seok Choi
出处
期刊:Small
[Wiley]
日期:2025-11-18
卷期号:: e08098-e08098
标识
DOI:10.1002/smll.202508098
摘要
Abstract Unconventional phase transformations reveal new crystallization mechanisms, yet direct observation of such pathways during nanoscale solution‐phase synthesis remains challenging. This study uncovers an atypical growth process in which thermodynamically stable CuI nanoparticles (NPs) transform into high‐energy 2D Cu plates. Using a combination of in situ transmission electron microscopy, ex situ structural analysis, and density functional theory calculations shows that the formation of structural defects induced by hexadecylamine and chloride ions facilitates the transformation by promoting surface iodine vacancies. The resulting Cu{111} nanoplates, with ultrathin thicknesses (≈4 nm) and exceptionally high aspect ratios (≈450), display enhanced oxidation resistance and long‐term stability under ambient conditions. This resistance is attributed to the close‐packed {111} facets, which suppress chemical oxidation even after extended exposure to air over 100 days. These findings provide new insights into non‐classical crystallization pathways in metal nanomaterials and suggest a versatile approach for preparing oxidation‐resistant, structurally defined Cu nanostructures.
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