{"title":"Secondary sulfidation-engineered Co/N–graphene catalyst for boosted ORR/OER bifunctionality in zinc–air batteries","authors":"Changlei Xia, Hongjie Chen, DongDong Wang, Shilei Ding","doi":"10.1016/j.electacta.2025.147607","DOIUrl":null,"url":null,"abstract":"<div><div>The development of highly efficient and stable bifunctional catalysts is of crucial importance for advancing the large-scale application of zinc-air batteries (ZABs). This present study introduces a composite catalyst composed of cobalt-based sulfides supported on nitrogen-doped graphene (Co@NG-S2), synthesized through a two-step sulfurization strategy. The first sulfurization stage was successful in achieving co-doping of sulfur (S) and nitrogen (N) while enhancing the conductivity and activity of the graphene support. The second sulfurization step promoted the uniform distribution of cobalt-based sulfides and strengthened their interfacial coupling with graphene, thereby significantly improving their bifunctional catalytic performance. Electrochemical characterization revealed that Co@NG-S2 exhibited an oxygen reduction reaction (ORR) onset potential of 0.868 V and a half-wave potential (E<sub>1/2</sub>) of 0.798 V (vs. RHE). For the oxygen evolution reaction (OER), Co@NG-S2 demonstrated a low overpotential of merely 430 mV at a current density of 10 mA cm<sup>-2</sup>, thereby demonstrating exceptional ORR/OER bifunctional activity. In addition, a liquid ZAB assembled with this catalyst achieved a peak power density of 110 mW cm<sup>-2</sup> and exhibited cycling stability exceeding 200 h. This study proposes a novel strategy for the synthesis of high-performance transition metal sulfide-carbon-based catalysts, demonstrating considerable promise for future applications.</div></div>","PeriodicalId":305,"journal":{"name":"Electrochimica Acta","volume":"543 ","pages":"Article 147607"},"PeriodicalIF":5.6000,"publicationDate":"2025-10-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Electrochimica Acta","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0013468625019644","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ELECTROCHEMISTRY","Score":null,"Total":0}
引用次数: 0
Abstract
The development of highly efficient and stable bifunctional catalysts is of crucial importance for advancing the large-scale application of zinc-air batteries (ZABs). This present study introduces a composite catalyst composed of cobalt-based sulfides supported on nitrogen-doped graphene (Co@NG-S2), synthesized through a two-step sulfurization strategy. The first sulfurization stage was successful in achieving co-doping of sulfur (S) and nitrogen (N) while enhancing the conductivity and activity of the graphene support. The second sulfurization step promoted the uniform distribution of cobalt-based sulfides and strengthened their interfacial coupling with graphene, thereby significantly improving their bifunctional catalytic performance. Electrochemical characterization revealed that Co@NG-S2 exhibited an oxygen reduction reaction (ORR) onset potential of 0.868 V and a half-wave potential (E1/2) of 0.798 V (vs. RHE). For the oxygen evolution reaction (OER), Co@NG-S2 demonstrated a low overpotential of merely 430 mV at a current density of 10 mA cm-2, thereby demonstrating exceptional ORR/OER bifunctional activity. In addition, a liquid ZAB assembled with this catalyst achieved a peak power density of 110 mW cm-2 and exhibited cycling stability exceeding 200 h. This study proposes a novel strategy for the synthesis of high-performance transition metal sulfide-carbon-based catalysts, demonstrating considerable promise for future applications.
期刊介绍:
Electrochimica Acta is an international journal. It is intended for the publication of both original work and reviews in the field of electrochemistry. Electrochemistry should be interpreted to mean any of the research fields covered by the Divisions of the International Society of Electrochemistry listed below, as well as emerging scientific domains covered by ISE New Topics Committee.