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源自COF@MOF杂化物的核壳碳基双功能电催化剂用于先进的可充电锌空气电池

Core-Shell Carbon-Based Bifunctional Electrocatalysts Derived from COF@MOF Hybrid for Advanced Rechargeable Zn-Air Batteries.

作者信息

Li Wei, Wang Jingyun, Chen Junxiang, Chen Kai, Wen Zhenhai, Huang Aisheng

机构信息

Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering, East China Normal University, Dongchuan Road 500, Shanghai, 200241, China.

CAS Key Laboratory of Design and Assembly of Functional Nanostructures, Fujian Provincial Key Laboratory of Nanomaterials, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, 350002, China.

出版信息

Small. 2022 Aug;18(31):e2202018. doi: 10.1002/smll.202202018. Epub 2022 Jul 9.

Abstract

The development of highly active carbon-based bifunctional electrocatalysts for both the oxygen evolution reaction (OER) and oxygen reduction reaction (ORR) is highly desired, but still full of challenges in rechargeable Zn-air batteries. Metal organic frameworks (MOFs) and covalent organic frameworks (COFs) have gained great attention for various applications due to their attractive features of structural tunability, high surface area and high porosity. Herein, a core-shell structured carbon-based hybrid electrocatalyst (H-NSC@Co/NSC), which contains high density active sites of MOF-derived shell (Co/NSC) and COF-derived hollow core (H-NSC), is successfully fabricated by direct pyrolysis of covalently-connected COF@ZIF-67 hybrid. The core-shell H-NSC@Co/NSC hybrid manifests excellent catalytic properties toward both OER and ORR with a small potential gap (∆E = 0.75 V). The H-NSC@Co/NSC assembled Zn-air battery exhibits a high power-density of 204.3 mW cm and stable rechargeability, outperforming that of Pt/C+RuO assembled Zn-air battery. Density functional theory calculations reveal that the electronic structure of the carbon frameworks on the Co/NSC shell can be effectively modulated by the embedded Co nanoparticles (NPs), facilitating the adsorption of oxygen intermediates and leading to enhanced catalytic activity. This work will provide a strategy to design highly-efficient electrocatalysts for application in energy conversion and storage.

摘要

人们迫切希望开发出用于析氧反应(OER)和氧还原反应(ORR)的高活性碳基双功能电催化剂,但在可充电锌空气电池中仍面临诸多挑战。金属有机框架(MOF)和共价有机框架(COF)因其结构可调性、高表面积和高孔隙率等吸引人的特性而在各种应用中备受关注。在此,通过共价连接的COF@ZIF-67杂化物的直接热解,成功制备了一种核壳结构的碳基混合电催化剂(H-NSC@Co/NSC),其包含MOF衍生的壳层(Co/NSC)的高密度活性位点和COF衍生的中空核(H-NSC)。核壳结构的H-NSC@Co/NSC杂化物对OER和ORR均表现出优异的催化性能,且电位差小(∆E = 0.75 V)。由H-NSC@Co/NSC组装的锌空气电池表现出204.3 mW cm的高功率密度和稳定的可充电性,优于由Pt/C+RuO组装的锌空气电池。密度泛函理论计算表明,Co/NSC壳层上碳框架的电子结构可通过嵌入的钴纳米颗粒(NP)有效调节,促进氧中间体的吸附并提高催化活性。这项工作将为设计用于能量转换和存储的高效电催化剂提供一种策略。

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