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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.
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页码:29551 / 29557
页数:7
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