Lixia Wang , Jiasui Huang , Jia Huang , Bowen Yao , Aling Zhou , Zhiyang Huang , Tayirjan Taylor Isimjan , Bao Wang , Xiulin Yang
{"title":"Promoting oxygen reduction reaction kinetics through manipulating electron redistribution in CoP/Cu3P@NC for aqueous/flexible Zn–air batteries†","authors":"Lixia Wang , Jiasui Huang , Jia Huang , Bowen Yao , Aling Zhou , Zhiyang Huang , Tayirjan Taylor Isimjan , Bao Wang , Xiulin Yang","doi":"10.1039/d4gc05538a","DOIUrl":null,"url":null,"abstract":"<div><div>Zinc–air batteries (ZABs) are considered a promising energy storage technology due to their high energy density and environmental friendliness. However, the development of efficient and durable oxygen reduction reaction (ORR) catalysts remains a challenge. Herein, we report the synthesis of a highly efficient CoP/Cu<sub>3</sub>P@NC catalyst using a Zn-MOF template, which was transformed into N- and C-doped bimetallic phosphides <em>via</em> high-temperature phosphating. The CoP/Cu<sub>3</sub>P@NC-based ZAB exhibits remarkable performance with an open-circuit voltage of 1.50 V, a peak power density of 215 mW cm<sup>−2</sup>, and a specific capacity of 691 mA h g<sub>zn</sub><sup>−1</sup>, outperforming conventional Pt/C-based ZABs. The catalyst maintained 93.5% of its initial activity after 300 h of cycling, demonstrating its excellent long-term stability. Furthermore, CoP/Cu<sub>3</sub>P@NC was applied in flexible ZABs, achieving a power density of 74 mW cm<sup>−2</sup> and showing stable performance under various bending conditions. The superior performance is attributed to the synergistic effects of Co and Cu, optimized structural properties, and high porosity, enhancing mass transfer and oxygen activation. These results suggest that CoP/Cu<sub>3</sub>P@NC is a highly promising ORR catalyst for next-generation ZABs, offering both high efficiency and durability in flexible and conventional energy storage applications.</div></div>","PeriodicalId":78,"journal":{"name":"Green Chemistry","volume":"27 8","pages":"Pages 2276-2285"},"PeriodicalIF":9.3000,"publicationDate":"2025-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Green Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S1463926225000627","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Zinc–air batteries (ZABs) are considered a promising energy storage technology due to their high energy density and environmental friendliness. However, the development of efficient and durable oxygen reduction reaction (ORR) catalysts remains a challenge. Herein, we report the synthesis of a highly efficient CoP/Cu3P@NC catalyst using a Zn-MOF template, which was transformed into N- and C-doped bimetallic phosphides via high-temperature phosphating. The CoP/Cu3P@NC-based ZAB exhibits remarkable performance with an open-circuit voltage of 1.50 V, a peak power density of 215 mW cm−2, and a specific capacity of 691 mA h gzn−1, outperforming conventional Pt/C-based ZABs. The catalyst maintained 93.5% of its initial activity after 300 h of cycling, demonstrating its excellent long-term stability. Furthermore, CoP/Cu3P@NC was applied in flexible ZABs, achieving a power density of 74 mW cm−2 and showing stable performance under various bending conditions. The superior performance is attributed to the synergistic effects of Co and Cu, optimized structural properties, and high porosity, enhancing mass transfer and oxygen activation. These results suggest that CoP/Cu3P@NC is a highly promising ORR catalyst for next-generation ZABs, offering both high efficiency and durability in flexible and conventional energy storage applications.
期刊介绍:
Green Chemistry is a journal that provides a unique forum for the publication of innovative research on the development of alternative green and sustainable technologies. The scope of Green Chemistry is based on the definition proposed by Anastas and Warner (Green Chemistry: Theory and Practice, P T Anastas and J C Warner, Oxford University Press, Oxford, 1998), which defines green chemistry as the utilisation of a set of principles that reduces or eliminates the use or generation of hazardous substances in the design, manufacture and application of chemical products. Green Chemistry aims to reduce the environmental impact of the chemical enterprise by developing a technology base that is inherently non-toxic to living things and the environment. The journal welcomes submissions on all aspects of research relating to this endeavor and publishes original and significant cutting-edge research that is likely to be of wide general appeal. For a work to be published, it must present a significant advance in green chemistry, including a comparison with existing methods and a demonstration of advantages over those methods.