双金属片
等离子体子
化学
纳米颗粒
贵金属
纳米技术
表面等离子共振
铂金
纳米棒
催化作用
纳米材料
等离子纳米粒子
材料科学
光电子学
生物化学
作者
Chang Sheng Xia,He Wei,Xiao Yang,Peng Fei Gao,Shu Jun Zhen,Yuan Fang Li,Cheng Zhi Huang
出处
期刊:Analytical Chemistry
[American Chemical Society]
日期:2022-09-21
卷期号:94 (39): 13440-13446
被引量:28
标识
DOI:10.1021/acs.analchem.2c02434
摘要
Plasmon-driven catalysis of metal nanostructures has garnered wide interest. Here, a photogenerated plasmonic hot-electron painting strategy was reported to form Au@Pt composite nanoparticles (Au@Pt NPs) with high catalytic reactivity without using reducing agents. Au nanoparticles, including Au nanospheres (Au NSs), Au nanorods (Au NRs), and Au nanobipyramids (Au NBPs), generated hot electrons under localized surface plasmon resonance (LSPR) excitation, which made the platinum precursor reduced as a consequence that Pt(0) atoms were painted on the surface of Au NPs to form an asymmetric Pt shell outside the plasmonic Au core. Compared with bare Au NPs, Au@Pt NPs exhibited significantly enhanced electrocatalytic activity toward reduction of H2O2 due to the bimetallic synergistic effect and great dispersion of Au@Pt NP-modified indium tin oxide (Au@Pt NPs/ITO). It exhibited a linear detection of H2O2 in a wide concentration range from 0.5 to 1000 μM with a low detection limit of 0.11 μM (S/N = 3). Therefore, the plasmonic hot-electron-painted Au@Pt NPs represent a novel and simple method for the design of advanced noble asymmetric metal nanomaterials.
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