Tailoring the Electrochemical Responses of MOF‐74 Via Dual‐Defect Engineering for Superior Energy Storage

Author:

Chen Tingting1ORCID,Xu Hengyue2ORCID,Li Shaopeng1,Zhang Jiaqi1ORCID,Tan Zhicheng1,Chen Long1,Chen Yiwang3,Huang Zhongjie1ORCID,Pang Huan4ORCID

Affiliation:

1. State Key Laboratory for Modification of Chemical Fibers and Polymer Materials College of Materials Science and Engineering Donghua University Shanghai 201620 China

2. Tsinghua Shenzhen International Graduate School Tsinghua University Shenzhen 518055 China

3. National Engineering Research Center for Carbohydrate Synthesis/Key Lab of Fluorine and Silicon for Energy Materials and Chemistry of Ministry of Education Jiangxi Normal University 99 Ziyang Avenue Nanchang 330022 China

4. School of Chemistry and Chemical Engineering Yangzhou University Yangzhou 225000 China

Abstract

AbstractRationally designed defects in a crystal can confer unique properties. This study showcases a novel dual‐defects engineering strategy to tailor the electrochemical response of metal–organic framework (MOF) materials used for electrochemical energy storage. Salicylic acid (SA) is identified as an effective modulator to control MOF‐74 growth and induce structural defects, and cobalt cation doping is adopted for introducing a second type of defect. The resulting dual‐defects engineered bimetallic MOF exhibits a discharging capacity of 218.6 mAh g−1, 4.4 times that of the pristine MOF‐74, and significantly improved cycling stability. Moreover, the engineered MOF‐74(Ni0.675Co0.325)‐8//Zn aqueous battery shows top energy/power density performances for Ni–Zn batteries (266.5 Wh kg−1, 17.22 kW kg−1). Comprehensive investigations reveal that engineered defects modify the local coordination environment and promote the in situ electrochemical reconfiguration during operation to significantly boost the electrochemical activity. This work suggests that rational tailoring of the defects within the MOF crystal is an effective strategy to manipulate the coordination environment of the metal centers and the corresponding electrochemical reconfiguration for electrochemical applications.

Funder

National Natural Science Foundation of China

State Key Laboratory for Modification of Chemical Fibers and Polymer Materials

Publisher

Wiley

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