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Hierarchical N-Doped Co/Carbon Heterostructures with Tunable Selectivity for H2O2 Production from Air
被引:0
|作者:
Cheng, Jinhuan
[1
]
Zhang, Shinan
[2
,3
]
Xu, Dong
[2
,3
]
Li, Qiyuan
[2
,3
]
Xia, Siyuan
[2
,3
]
Zhai, Guangyao
[2
,3
]
Gao, Peng
[2
,3
]
Hu, Weiyao
[2
,3
]
Liang, Jianxing
[1
]
Jia, Jinping
[1
]
机构:
[1] Shanghai Jiao Tong Univ, Sch Environm Sci & Engn, Shanghai 200240, Peoples R China
[2] Shanghai Jiao Tong Univ, Chem & Chem Engn, Shanghai 200240, Peoples R China
[3] Shanghai Jiao Tong Univ, Frontiers Sci Ctr Transformat Mol, Shanghai 200240, Peoples R China
基金:
中国国家自然科学基金;
关键词:
aerophilic hierarchical structure;
tunableselectivityfor H2O2;
selective oxygen reduction;
electrochemical H2O2 synthesis;
Mott-Schottky interface;
HYDROGEN-PEROXIDE;
OXYGEN REDUCTION;
METAL NANOPARTICLES;
OXIDATION;
GRAPHENE;
WATER;
CATALYSTS;
GENERATION;
ELECTRODE;
CARBONS;
D O I:
10.1021/acssuschemeng.3c04005
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
As a green oxidant, H2O2 can be produced via the electrochemical reduction of oxygen. However, current techniques usually require high-pressure air or oxygen gas to accelerate the oxygen diffusion via bubbling in the electrolyte. Here, we design a multifunctional gas capture catalyst (GCC) of hierarchical N-doped Co/carbon heterostructures with a Schottky contact at the interface for the highly efficient capture and selective transformation of oxygen from air to H2O2. Tuning the Schottky contact at the Co/NxC interface boosts H2O2 production in acid media. Remarkably, as the catalyst in the H-cell without an ion-exchange membrane and a polytetrafluoroethylene (PTFE) assistant, the Co/N2.1C GCC could provide an accumulated H2O2 yield of 2413 mg L-1 h(-1) (730 mmol g(-1) h(-1)) at 20 mA cm(-2) in 0.1 M HClO4 solution under natural air diffusion. More importantly, consistent Faradaic efficiencies (75%) at a wide scope of working potentials ranging from -0.54 to 0.46 V vs RHE were attained. The connected hierarchical structure of Co/N2.1C GCC remains stable without an obvious flooding effect confronted by conventional gas flow electrodes. This work affords valuable information for fabricating highly efficient 2e(-) ORR catalysts and expands heterojunction catalysts for H2O2 production.
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页码:16491 / 16498
页数:8
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