Functionalized Copper Nanoparticles with Gold Nanoclusters: Part I. Highly Selective Electrosynthesis of Hydrogen Peroxide

被引:3
|
作者
Luo, Kun [1 ]
Li, Ya [1 ]
Liu, Tong [1 ]
Zhuge, Xiangqun [1 ]
Chung, Etelka [2 ]
Timms, Andrew R. [2 ]
Graham, Simon P. [3 ]
Ren, Guogang [2 ]
机构
[1] Changzhou Univ, Sch Mat Sci & Engn, Changzhou 213164, Peoples R China
[2] Univ Hertfordshire, Hatfield AL10 9AB, Herts, England
[3] Pirbright Inst, Woking GU24 0NF, Surrey, England
来源
ACS OMEGA | 2023年 / 8卷 / 39期
基金
中国国家自然科学基金; 英国生物技术与生命科学研究理事会;
关键词
OXYGEN REDUCTION; H2O2; ELECTROCATALYSIS; PROSPECTS; WATER; CU;
D O I
10.1021/acsomega.3c03665
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Copper nanoparticles (CuNPs) and gold nanoclusters (AuNCs) show a high catalytic performance in generating hydrogen peroxide (H2O2), a property that can be exploited to kill disease-causing microbes and to carry carbon-free energy. Some combinations of NPs/NCs can generate synergistic effects to produce stronger antiseptics, such as H(2)O(2)or other reactive oxygen species (ROS). Herein, we demonstrate a novel facile AuNC surface decoration method on the surfaces of CuNPs using galvanic displacement. The Cu-Au bimetallic NPs presented a high selective production of H(2)O(2)via a two-electron (2e(-)) oxygen reduction reaction (ORR). Their physicochemical analyses were conducted by scanning electron microscopy (SEM), transmitting electron microscopy (TEM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). With the optimized Cu-Au(1.5)NPs showing their particle sizes averaged in 53.8 nm, their electrochemical analysis indicated that the pristine AuNC structure exhibited the highest 2e- selectivity in ORR, the CuNPs presented the weakest 2e- selectivity, and the optimized Cu-Au(1.5)NPs exhibited a high 2e- selectivity of 95% for H2O2 production, along with excellent catalytic activity and durability. The optimized Cu-Au(1.5)NPs demonstrated a novel pathway to balance the cost and catalytic performance through the appropriate combination of metal NPs/NCs.
引用
收藏
页码:36171 / 36178
页数:8
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