Synergistically Interactive Pyridinic-N-MoP Sites: Identified Active Centers for Enhanced Hydrogen Evolution in Alkaline Solution

被引:360
作者
Zhao, Di [1 ]
Sun, Kaian [1 ,2 ]
Cheong, Weng-Chon [1 ]
Zheng, Lirong [1 ,3 ]
Zhang, Chao [1 ]
Liu, Shoujie [1 ]
Cao, Xing [1 ]
Wu, Konglin [1 ]
Pan, Yuan [1 ]
Zhuang, Zewen [1 ]
Hu, Botao [1 ]
Wang, Dingsheng [1 ]
Peng, Qing [1 ]
Chen, Chen [1 ]
Li, Yadong [1 ]
机构
[1] Tsinghua Univ, Dept Chem, Beijing 100084, Peoples R China
[2] China Univ Petr East China, State Key Lab Heavy Oil Proc, Qingdao 266580, Shandong, Peoples R China
[3] Chinese Acad Sci, Inst High Energy Phys, Beijing Synchrotron Radiat Facil, Beijing 100049, Peoples R China
基金
北京市自然科学基金; 中国博士后科学基金; 中国国家自然科学基金; 国家重点研发计划;
关键词
carbon shells; electrocatalysis; hydrogen evolution reaction; MoP nanoparticles; N-doped carbon; OXYGEN REDUCTION; HIGHLY EFFICIENT; MOLYBDENUM PHOSPHIDE; CATALYTIC-ACTIVITY; COBALT OXIDE; LOW-COST; NITROGEN; GRAPHENE; NANOPARTICLES; ELECTROCATALYST;
D O I
10.1002/anie.201908760
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
For electrocatalysts for the hydrogen evolution reaction (HER), encapsulating transition metal phosphides (TMPs) into nitrogen-doped carbon materials has been known as an effective strategy to elevate the activity and stability. Yet still, it remains unclear how the TMPs work synergistically with the N-doped support, and which N configuration (pyridinic N, pyrrolic N, or graphitic N) contributes predominantly to the synergy. Here we present a HER electrocatalyst (denoted as MoP@NCHSs) comprising MoP nanoparticles encapsulated in N-doped carbon hollow spheres, which displays excellent activity and stability for HER in alkaline media. Results of experimental investigations and theoretical calculations indicate that the synergy between MoP and the pyridinic N can most effectively promote the HER in alkaline media.
引用
收藏
页码:8982 / 8990
页数:9
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