电催化剂
过电位
选择性
电化学
电子转移
材料科学
铂金
化学工程
原电池
金属
催化作用
溶解
纳米技术
化学
物理化学
冶金
电极
有机化学
工程类
作者
Qiurong Shi,Wenlei Zhu,Hong Zhong,Chengzhou Zhu,Hangyu Tian,Jincheng Li,Mingjie Xu,Dong Su,Xing Li,Dong Liu,Bo Xu,Scott P. Beckman,Dan Du,Yuehe Lin
标识
DOI:10.1021/acsaem.9b01314
摘要
The electrochemical production of hydrogen peroxide is enjoying increasing attention by endowing a promising alternative to the traditional complex and energy-intensive anthraquinone process. Engineering efficient electrocatalysts with desirable activity, selectivity, and stability toward H2O2 electrocatalysis have achieved great progress yet are still challenging. Currently, atomically dispersed Pt atoms on metal have been evidenced as one of the most efficient candidates for their remarkable catalytic activity and selectivity toward H2O2 production through a two electron transfer path for oxygen reduction reaction. Here, atomically dispersed Pt atoms are successfully anchored on the surface of AuCu ultrathin nanowire aerogels (denoted as AD-Pt@AuCu) through kinetically controlled galvanic replacement reaction. The composition-optimized AD-Pt@AuCu-144 behaved in a thermodynamically favorable two electron transfer path rather than four as evidenced by a lower thermodynamical overpotential based on first-principles calculation. The H2O2 selectivity reached 91.8% and achieved a continuous yield of 47.5 mg/L H2O2 in 5 h, owing to its unique atomic configuration and robust 3D porous architecture. The AD-Pt@AuCu-144 catalysts may pave a way for favoring the advances of localized electrochemical production of H2O2.
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