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.
引用
收藏
页码:16491 / 16498
页数:8
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