Efficient Electrochemical Production of H2O2 on Hollow N-Doped Carbon Nanospheres with Abundant Micropores

被引:91
|
作者
Hu, Yezhou [1 ]
Zhang, Jingjing [1 ]
Shen, Tao [1 ]
Li, Zhengrong [1 ]
Chen, Ke [1 ]
Lu, Yun [1 ]
Zhang, Jian [1 ]
Wang, Deli [1 ]
机构
[1] Huazhong Univ Sci & Technol, Key Lab Mat Chem Energy Convers & Storage, Minist Educ,Sch Chem & Chem Engn, Hubei Key Lab Mat Chem & Serv Failure, Wuhan 430074, Peoples R China
关键词
two-electron oxygen reduction reaction; carbon-based electrocatalysts; electrochemical H2O2 production; self-templating strategy; hollow N-doped carbon spheres; OXYGEN-REDUCTION; HYDROGEN-PEROXIDE; POROUS CARBON; SIZE; ELECTROCATALYSTS; SELECTIVITY; CATALYSTS; ALKALINE; HYBRIDS;
D O I
10.1021/acsami.1c05353
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Electrocatalytic two-electron (2e(-)) oxygen reduction reaction (ORR) has been regarded as an efficient strategy to achieve onsite H2O2 generation under ambient conditions. However, due to the sluggish kinetics and competitive reaction between 2e(-) and 4e(-) ORR, exploring more efficient ORR catalysts with dominant 2e(-) ORR selectivity is of significance. Herein, hollow N-doped carbon spheres (HNCS) with abundant micropores through a template-directed method are presented. Consequently, the selectivity of the HNCS reaches similar to 91.9% at 0.7 V (vs RHE), and the output for H2O2 production is up to 618.5 mmol g(catalyst)(-1) h(-1) in 0.1 M KOH solution. The enhanced performance of HNCS for H2O2 electrosynthesis could be attributed to the hollow structure and heteroatom/defect/pore incorporation. The strategy presented here could shed light on the design of efficient carbon-based materials for improved 2e(-) ORR.
引用
收藏
页码:29551 / 29557
页数:7
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