Investigation of Transition Metal-Based (Mn, Co, Ni, Fe) Trimetallic Oxide Nanoparticles on N-doped Carbon Nanotubes as Bifunctional Catalysts for Zn-Air Batteries
Investigation of Transition Metal-Based (Mn, Co, Ni, Fe) Trimetallic Oxide Nanoparticles on N-doped Carbon Nanotubes as Bifunctional Catalysts for Zn-Air Batteries
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DOI:
10.1149/1945-7111/ab7094
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发表时间:
2020-02-11
影响因子:
3.9
通讯作者:
Ivey, Douglas G.
中科院分区:
文献类型:
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作者:
Aasen, Drew;Clark, Michael P.;Ivey, Douglas G.
Various transition metal-based bimetallic and trimetallic oxides on N-CNTs were successfully synthesized in a one-pot process. Porous gas diffusion layers (GDLs) were simultaneously impregnated with the catalysts during synthesis, resulting in an efficient and scalable preparation technique for nano-composite air electrodes. NiMnOx/N-CNT, NiFeOx/N-CNT, and (Co,Fe)(3)O-4/N-CNT catalysts were the highest performing bimetallic oxides based on battery rate test results. Therefore, Ni-Co-Fe, Ni-Mn-Fe, and Mn-Co-Fe systems were investigated as combined trimetallic oxide/N-CNT catalysts for Zn-air batteries. Trimetallic oxides on N-CNTs exhibited improved OER activity and comparable ORR activity relative to the bimetallic oxide catalysts in linear sweep voltammetry (LSV) tests. Discharge/charge efficiencies for tri-metallic oxides on N-CNTs calculated from battery rate test measurements at a current density of 20 mA cm(-2) were 60.5%, 60.7%, and 60.0% for NCFO/N-CNT, NMFO/N-CNTs and MCFO/N-CNT, respectively. Bifunctional cycling of all trimetallic oxide/N-CNT electrodes at 10 mA cm(-2) for 100 h showed excellent stability, particularly the NCFO/N-CNT catalyst. Additionally, the efficiencies for NCFO/N-CNT, NMFO/N-CNT and MCFO/N-CNT samples were 58.5%, 57.9% and 57.2%, respectively, after cycling, which compare favorably with that of Pt-Ru/C (55.3%). Trimetallic oxides on N-CNTs are, therefore, excellent candidates as high performing, non-precious metal catalysts for Zn-air batteries. (C) 2020 The Electrochemical Society ("ECS"). Published on behalf of ECS by IOP Publishing Limited.