铜
化学
纳米颗粒
催化作用
胶体金
壳体(结构)
化学工程
原电池
纳米结构
合金
纳米技术
材料科学
复合材料
物理化学
有机化学
工程类
作者
Shaonan Tian,Yu Zhang,Qing Zeng,Junyu Zhong,Hui Liu,Lin Xu,Jun Yang
出处
期刊:Chinese Journal of Structural Chemistry
日期:2023-11-01
卷期号:42 (11): 100160-100160
被引量:1
标识
DOI:10.1016/j.cjsc.2023.100160
摘要
Core-shell nanostructures usually exhibit tunable catalytic properties in comparison with their single core or shell counterpart due to electronic interaction and lattice strain between the core and shell regions. Herein, we report the intriguing evolution of copper (Cu) shells on the gold (Au) cores at different Au/Cu precursor ratios during the synthesis of core-shell Au–Cu nanoparticles at an organic medium via seed-mediated growth method. In brief, at relatively low Cu ratios, quasi-spherical Au–Cu nanoparticles with conventional core-shell structures are the majority products, in which the Cu shell thickness increases with the increase of Cu precursor ratios. The difference is that at high Cu ratios, the Cu shells no longer increase their thickness, but evolve into a dendritic structure. Interestingly, the core-shell Au–Cu nanoparticles with dendritic Cu shells could be transformed into interesting Au–Cu cage-bell structures after a ripening process at elevated temperature. Further, through galvanic replacement reaction with Pt precursors, the thin Cu shells could be converted into CuPt alloy shells on the Au cores, which exhibit enhanced activity towards methanol oxidation reaction with satisfactory durability, in comparison with that of commercial Pt/C catalysts.
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