Catalyst Design for Electrochemical Oxygen Reduction toward Hydrogen Peroxide

被引:204
|
作者
Jiang, Kun [1 ]
Zhao, Jiajun [1 ]
Wang, Haotian [2 ,3 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Mech Engn, Interdisciplinary Res Ctr, Inst Fuel Cells, Shanghai 200433, Peoples R China
[2] Rice Univ, Dept Chem & Biomol Engn, Houston, TX 77005 USA
[3] Canadian Inst Adv Res CIFAR, 22 Ontario, Toronto, ON M5G 1M1, Canada
关键词
electrocatalysis; hydrogen peroxide; oxygen reduction reaction; platinum; single atom catalysts; HIGH ELECTROCATALYTIC ACTIVITY; DOPED MESOPOROUS CARBON; DIRECT H2O2 PRODUCTION; FUEL-CELL CATALYST; METAL-CATALYSTS; ALKALINE ELECTROLYTE; HIGHLY EFFICIENT; PT/C CATALYST; PLATINUM; NITROGEN;
D O I
10.1002/adfm.202003321
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Precise electrochemical synthesis under ambient conditions has provided emerging opportunities for renewable energy utilization. Among many promising systems, the production of hydrogen peroxide (H2O2) from the cathodic oxygen reduction reaction (ORR) has attracted considerable interest in past decades due to the increasing market demands and the vital role of ORR in the electrocatalysis field. This work describes recent advances in cathodic materials for H(2)O(2)synthesis from 2e(-)ORR. By using Pt as a stereotype, the tuning knobs are overviewed, including the intrinsic binding strength of oxygenated species, the intermediate diffusion path and the isolation of Pt-Pt ensembles that enable 2e(-)ORR pathway from 4e(-)total reduction. This knowledge is successfully applied to other transition metal systems and leads to the discovery of more efficient alloy catalysts with balanced improvement on both activity and selectivity. In addition, mesostructure engineering and heteroatoms doping strategies on carbon-based materials, which significantly boost the H(2)O(2)production efficiency as compared to intact carbon sites, are also reviewed. Finally, future directions and challenges of transferring developed catalysts from lab scale tests to pilot plant operations are briefly outlooked.
引用
收藏
页数:11
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