Localized Ligands Assist Ultrafast Multivalent‐Cation Intercalation Pseudocapacitance

Author:

Xie Luting1,Xu Kui2,Sun Wenlu1,Fan Yingzhu3,Zhang Junyu4,Zhang Yixiao5,Zhang Hui6,Chen Jun1,Shen Yanbin3,Fu Fang1,Kong Huabin1,Wu Guan7,Wu Jihuai1,Chen Liwei5,Chen Hongwei18ORCID

Affiliation:

1. College of Materials Science and Engineering Huaqiao University Xiamen 361021 China

2. School of Flexible Electronics (Future Technologies) & Institute of Advanced Materials (IAM) Nanjing University of Technology Nanjing 211816 China

3. i-Lab CAS Center for Excellence in Nanoscience Suzhou Institute of Nano-Tech and Nano-Bionics Chinese Academy of Sciences Suzhou 215123 Jiangsu Province China

4. Instrumental Analysis Center Laboratory and Equipment Management Department Huaqiao University Xiamen Fujian 361021 China

5. In-Situ Center for Physical Science School of Chemistry and Chemical Engineering Shanghai Jiaotong University Shanghai 200240 China

6. National Key Laboratory of High-efficiency Utilization of Coal and Green Chemical Engineering Ningxia University Yinchuan 750021 China

7. National Engineering Lab for Textile Fiber Materials and Processing Technology School of Materials Science and Engineering Zhejiang Sci-Tech University Hangzhou 310018 China

8. Department of Xiamen Key Laboratory of Optoelectronic Materials and Advanced Manufacturing College of Materials Science and Engineering Huaqiao University Xiamen 361021 China

Abstract

AbstractRechargeable batteries based on multivalent cation (Mvn+, n>1) carriers are considered potentially low‐cost alternatives to lithium‐ion batteries. However, the high charge‐density Mvn+ carriers generally lead to sluggish kinetics and poor structural stability in cathode materials. Herein, we report an Mvn+ storage via intercalation pseudocapacitance mechanism in a 2D bivalve‐like organic framework featured with localized ligands. By switching from conventional intercalation to localized ligand‐assisted‐intercalation pseudocapacitance, the organic cathode exhibits unprecedented fast kinetics with little structural change upon intercalation. It thus enables an excellent power density of 57 kW kg−1 over 20000 cycles for Ca2+ storage and a power density of 14 kW kg−1 with a long cycling life over 45000 cycles for Zn2+ storage. This work may provide a largely unexploited route toward constructing a local dynamic coordination microstructure for ultrafast Mvn+ storage.

Funder

Natural Science Foundation of Xiamen City

Natural Science Foundation of Jiangsu Province

Publisher

Wiley

Subject

General Chemistry,Catalysis

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