期刊
ACS SUSTAINABLE CHEMISTRY & ENGINEERING
卷 9, 期 1, 页码 510-520出版社
AMER CHEMICAL SOC
DOI: 10.1021/acssuschemeng.0c07890
关键词
heterointerface engineering; 3D network structure; bifunctional electrocatalysts; oxygen electrocatalysis; rechargeable Zn-air batteries
资金
- National Natural Science Foundation of China [21573115, 21875118]
- Natural Science Foundation of Tianjin [19JCZDJC37700]
- 111 project [B12015]
Designing and constructing highly efficient bifunctional electrocatalysts for oxygen reduction and oxygen evolution is crucial for the development of rechargeable Zn-air batteries. This study highlights the use of in situ heterointerface engineering and a three-dimensional porous network structure to prepare electrocatalysts with outstanding performance in oxygen electrocatalysis. The Co9S8/CoO heterojunction-induced destabilized charge distribution and well-designed 3D-interconnected network structure contribute to the exceptional oxygen electrocatalytic performance of Co-S-O/NSCN catalyst, showing great potential for applications in metal-air cathode electrocatalysts.
Designing and constructing highly efficient bifunctional electrocatalysts for oxygen reduction (ORR) and oxygen evolution (OER) is critical to the development of rechargeable Zn-air batteries. Taking into account the multistep electron-transfer process of oxygen electrocatalytic reactions, it is very desirable to design a suitable construction for electrocatalysts with fantastic electronic transport properties and structural advantages. Herein, we highlight in situ heterointerface engineering and a three-dimensional (3D) porous network structure in preparing the electrocatalysts of N,S-codoped 3D carbon matrix with Co9S8/CoO heterojunction (Co-S-O/NSCN). Systematic characterization and electrochemical experiments confirm that the destabilized charge distribution induced by the Co9S8/CoO heterojunction promotes the fast transfer of electrons during the electrocatalytic process. The well-designed 3D-interconnected network structure composed of 2D nanosheets and in situ-generated 1D carbon nanotubes facilitates the multidimensional electron delivery and reactant migration, along with other additional structural advantages of high surface area and enhanced electronic conductivity. Benefiting from these significant advantages, Co-S-O/NSCN exhibits outstanding oxygen electrocatalytic performance with the ORR half-wave potential of 0.865 V, the OER potential of 1.665 Vat 10 mA cm(-2) (ORR-OER potential gap of 0.80 V), and extraordinary durability in 0.1 M KOH, outperforming the noble-metal Pt/C catalyst and most of the reported Co-based electrocatalysts. Impressively, both the rechargeable Zn-air batteries using liquid and solid electrolytes, assembled by Co-S-O/NSCN catalysts, show satisfactory performance with low charge-discharge gap and long cycling life. This work highlights the superiority of the heterointerface and advanced structural configuration in oxygen electrochemistry, thus giving some inspiration for the fabrication of significant metal-air cathode electrocatalysts.
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