Nanoflower-like NiCo2O4 Composite Graphene Oxide as a Bifunctional Catalyst for Zinc-Air Battery Cathode

被引:2
|
作者
Fu, Lixiang [1 ]
Yao, Yifan [1 ]
Ma, Jingling [1 ,2 ]
Zhang, Zhikang [1 ]
Wang, Guangxin [1 ,2 ]
Wei, Weifeng [1 ]
机构
[1] Henan Univ Sci & Technol, Res Ctr High Pur Mat, Luoyang 471023, Peoples R China
[2] Prov & Minist Coconstruct Collaborat Innovat Ctr N, Luoyang 471023, Peoples R China
基金
中国国家自然科学基金;
关键词
ENHANCED ELECTROCATALYTIC ACTIVITIES; ONE-POT SYNTHESIS; OXYGEN REDUCTION; EFFICIENT ELECTROCATALYST; ULTRATHIN NANOSHEETS; MESOPOROUS NICO2O4; SUPPORTED COFE2O4; PERFORMANCE; EVOLUTION; HYBRID;
D O I
10.1021/acs.langmuir.4c00018
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Developing efficient bifunctional catalysts for nonprecious metal-based oxygen reduction (ORR) and oxygen evolution (OER) is crucial to enhance the practical application of zinc-air batteries. The study harnessed electrostatic forces to anchor the nanoflower-like NiCo2O4 onto graphene oxide, mitigating the poor inherent conductivity in NiCo2O4 as a transition metal oxide and preventing excessive agglomeration of the nanoflower-like structures during catalysis. Consequently, the resulting composite, NiCo2O4-GO/C, exhibited notably superior ORR and OER catalytic performance compared to pure nanoflower-like NiCo2O4. Notably, it excelled in OER catalytic activity of the OER relative to the precious metal RuO2. As a bifunctional catalyst for ORR and OER, NiCo2O4-GO/C displayed a potential difference of 0.88 V between the ORR half-wave potential and the OER potential at 10 mA<middle dot>cm(-2), significantly lower than the 1.08 V observed for pure flower-like NiCo2O4 and comparable to the 0.88 V exhibited by precious metal catalysts Pt/C + RuO2. The NiCo2O4-GO/C-based zinc-air battery demonstrated a discharge capacity of 817.3 mA h<middle dot>g(-1), surpassing that of precious metal-based zinc-air batteries. Moreover, charge-discharge cycling tests indicated the superior stability of the NiCo2O4-GO/C-based zinc-air battery compared to its precious metal-based counterparts.
引用
收藏
页码:6990 / 7000
页数:11
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