材料科学
催化作用
纳米棒
咪唑酯
双功能
锌
沸石咪唑盐骨架
化学工程
金属有机骨架
多孔性
电池(电)
热解
氧气
析氧
碳纤维
电化学
电催化剂
纳米技术
无机化学
电极
吸附
冶金
有机化学
化学
复合材料
功率(物理)
物理化学
工程类
物理
复合数
量子力学
作者
Dezhang Ren,Jie Ying,Meiling Xiao,Ya‐Ping Deng,Jiahua Ou,Jianbing Zhu,Guihua Liu,Yi Pei,Shuang Li,Altamash M. Jauhar,Huile Jin,Shun Wang,Dong Su,Aiping Yu,Zhongwei Chen
标识
DOI:10.1002/adfm.201908167
摘要
Abstract The lack of efficient strategies to address the intrinsic activity, site accessibility, and structural stability issues of metal‐carbon hybrid catalysts is restricting their real‐world implementation on the basis of rechargeable zinc–air batteries. Herein, a dual metal–organic frameworks (MOFs) pyrolysis strategy is developed to regulate the intrinsic activity and porous structure of the derived catalysts, where a Fe 2 Ni_MIL‐88@ZnCo_zeolitic imidazolate framework (ZIF), with a hierarchically porous structure, multifunctional components, and an integrated architecture, acts as an ideal precursor to obtain multimetal based porous nanorod (FeNiCo@NC‐P). Benefitting from the synergetic effect of the multimetal components, facilitated reactant accessibility, and the well‐retained integrated structure, the resultant FeNiCo@NC‐P catalyst exhibits an oxygen reduction reaction half‐wave potential of 0.84 V as well as an oxygen evolution reaction potential of 1.54 V at 10 mA cm –2 . Furthermore, the practical application of FeNiCo@NC‐P in the zinc–air battery displays a low voltage gap and long‐term durability (over 130 h at a current density of 10 mA cm –2 ), which outperforms the commercial noble metal benchmarks. This work not only affords a competitive bifunctional oxygen electrocatalyst for zinc–air batteries but also paves a new way to design and fabricate MOF‐derived materials with tunable catalytic properties.
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