Molecular Engineering of N‐heteroaromatic Organic Cathode for High‐Voltage and Highly Stable Zinc Batteries

Author:

Yan Yichao12,Li Pei23,Wang Yiqiao23,Bi Leyu23,Lau Ting Wai4,Miao Mulin23,Yang Shuo23,Xiong Qi23,Lin Francis R12,Yip Hin‐Lap23,Yin Jun4,Zhi Chunyi23,Jen Alex K.‐Y.123ORCID

Affiliation:

1. Department of Chemistry City University of Hong Kong Kowloon 999077 Hong Kong

2. Hong Kong Institute for Clean Energy City University of Hong Kong Kowloon 999077 Hong Kong

3. Department of Materials Science and Engineering City University of Hong Kong Kowloon 999077 Hong Kong

4. Department of Applied Physics The Hong Kong Polytechnic University Kowloon Hung Hom 999077 Hong Kong

Abstract

AbstractZinc batteries hold promise for grid‐scale energy storage due to their safety and low cost. A key challenge for the field is identifying cathode materials that can undergo reversible redox reactions at the extreme potentials required for realizing high energy density devices. While organic materials have been extensively explored as cathode materials due to their structural tunability and eco‐friendliness, most reported zinc‐organic batteries exhibit a voltage lower than 1.2 V. In this report, by employing rational molecular design and synthesis, computational analysis, and electrochemical evaluation, the well‐studied neutral p‐type N‐centered is redesigned, triphenylamine organic cathode by replacing three phenyl rings with the smallest aromatic system – cationic cyclopropenium. This results in a novel class of cathode materials with simultaneously enhanced potential, capacity, and stability. The resultant full battery exhibits a high discharge voltage of 1.7 V and an outstanding capacity retention of 95% after 10000 cycles at a discharge capacity of 157.5 mAh g−1cation (103.9 mAh g−1salt).

Funder

Hong Kong Polytechnic University

University Grants Committee

Publisher

Wiley

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