二羟丙酮
甘油
催化作用
合金
纳米颗粒
Atom(片上系统)
化学
材料科学
核化学
化学工程
纳米技术
有机化学
计算机科学
工程类
嵌入式系统
作者
Tongyu Tang,Hai Zhang,Haofan Wang,Hongjuan Wang,Yonghai Cao,Lingyun Zhou,Hao Yu
出处
期刊:Chemical synthesis
[OAE Publishing Inc.]
日期:2025-02-24
卷期号:5 (2)
摘要
Nanoscale metal particle-decorated single-atom catalysts (SACs) have been widely used in the fields of photocatalysis, electrocatalysis and thermal catalysis due to the combination of the advantages of nanoparticles and SACs. Herein, a strategy based on Pt-Bi atomic exchange is proposed for the formation of ultrafine (sub-2 nm) PtBi nanoclusters on single atomic Bi-N-C. The dynamic structural evolution between single atomic Bi-N-C on nitrogen-doped carbon nanosheets and Pt nanoclusters on the reconfiguration of stable PtBi alloy nanoparticles was demonstrated through a spherical aberration-corrected transmission electron microscope, X-ray absorption spectroscopy and density functional theory calculations. By our synthesis strategy, the Bi-N-C sites significantly improve the dispersion of PtBi alloy nanoparticles, resulting in a high turnover frequency of up to 224.4 h-1 and the 1,3-dihydroxyacetone selectivity of 77.4%, 3.5 times higher than that of commercial 5Pt/C. On the other hand, the strong interaction between SAC and nanoparticles enhanced the catalytic stability by preventing leaching of Bi. It opens new avenues toward the rational design of high-performance nanoparticle-SACs, enabled by the in-depth understanding of the interaction between nanoparticles and SACs, which determines the structure of real active sites.
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