Self-grown layered double hydroxide nanosheets on bimetal-organic frameworks-derived N-doped CoOx carbon polyhedra for flexible all-solid-state rechargeable Zn-air batteries

被引:22
作者
Hao, Yaxin [1 ]
Kang, Yumao [1 ]
Kang, Huichun [1 ]
Xin, Hongyuan [1 ]
Liu, Fangqing [1 ]
Li, Lifang [1 ]
Wang, Wei [2 ]
Lei, Ziqiang [1 ]
机构
[1] Northwest Normal Univ, Coll Chem & Chem Engn, Key Lab Ecofunct Polymer Mat, Key Lab Polymer Mat Gansu Prov,Minist Educ, Lanzhou 730070, Peoples R China
[2] Lanzhou Jiaotong Univ, Sch Chem & Biol Engn, Lanzhou 730070, Peoples R China
基金
中国国家自然科学基金;
关键词
N-doping CoOx carbon polyhedra; NiFe LDH nanosheet; Metal-organic frameworks; Bifunctional catalysts; Zn-air battery; OXYGEN REDUCTION REACTION; BIFUNCTIONAL ELECTROCATALYSTS; EFFICIENT; CATALYSTS; ZIF-67; NANOPARTICLE; NANOCAGES; CLUSTERS;
D O I
10.1016/j.jpowsour.2022.231076
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The synthesis of non-precious metal electrocatalysts for oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) is essential for flexible rechargeable metal-air batteries. Herein, a novel LDH@N-CoOx@C bifunctional electrocatalyst was synthesized by a straightforward solution reaction, annealing process, and hydrothermal reaction. The material consisted of two-dimensional (2D) NiFe layered double hydroxide (LDH) nanosheets self-grown on N-doped CoOx carbon polyhedra derived from bimetal-organic frameworks. The outer LDH nanosheets effectively maintained the catalytic activity and long-term stability of the inner N-CoOx@C. The heterostructure formed by the LDH self-growth on N-CoOx@C and the strong electronic interaction between N-CoOx@C and LDH greatly promoted the OER and ORR activities. The LDH@N-CoOx@C exhibited a low overpotential of 273 mV at 10 mA cm(-2) for OER and a half-wave potential (E-1/2) close to the commercial Pt/C catalyst for ORR, demonstrating its excellent bifunctional catalytic performance. In addition, the LDH@N-CoOx@C catalyst showed a higher energy density and extraordinary stability in liquid Zn-air batteries (ZABs) compared with the commercial Pt/C + RuO2 catalyst, having good prospect in flexible all-solid-state ZABs.
引用
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页数:11
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