Enhanced oxygen evolution reaction performance of flower-like CoHS @NCDs through in-situ coupling of Nitrogen-Doped carbon dots and cobalt hydroxide nanosheets
Yang Gao , Haiyan Qi , Tao Jing , Jun Li , Siqi Shen , Qingxin Zeng , Hongxu Zhao
{"title":"Enhanced oxygen evolution reaction performance of flower-like CoHS @NCDs through in-situ coupling of Nitrogen-Doped carbon dots and cobalt hydroxide nanosheets","authors":"Yang Gao , Haiyan Qi , Tao Jing , Jun Li , Siqi Shen , Qingxin Zeng , Hongxu Zhao","doi":"10.1016/j.jelechem.2024.118858","DOIUrl":null,"url":null,"abstract":"<div><div>Efficient electrocatalytic materials are crucial for enhancing the efficiency of the oxygen evolution reaction (OER) in hydrolysis applications. In this study, we synthesized nitrogen-doped carbon dots (NCDs) via a straightforward one-step hydrothermal method. Subsequently, 3D flower-shaped CoHS@NCDs electrocatalysts were prepared by the integration of NCDs and cobalt hydroxide nanosheets (CoHS) using a solvothermal method. The resulting CoHS@NCDs electrocatalysts demonstrated outstanding catalytic performance for OER under alkaline conditions. Specifically, the CoHS@NCDs-3 electrocatalyst exhibited an overpotential of 280 mV at 10 mA cm<sup>−2</sup>(314 mV at 50 mA cm<sup>−2</sup>), representing an 80 mV improvement compared to CoHS, along with remarkable durability. Through comprehensive characterization, we revealed that the incorporation of NCDs facilitated the creation of numerous exposed active sites on CoHS, forming a unique electron transfer pathway (Co-N), thereby optimizing the kinetics of the OER reaction. This study underscored the significant potential of constructing electrocatalysts with exceptional OER activity based on transition metal hydroxides.</div></div>","PeriodicalId":355,"journal":{"name":"Journal of Electroanalytical Chemistry","volume":"977 ","pages":"Article 118858"},"PeriodicalIF":4.1000,"publicationDate":"2025-01-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Electroanalytical Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1572665724008373","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/12/7 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Efficient electrocatalytic materials are crucial for enhancing the efficiency of the oxygen evolution reaction (OER) in hydrolysis applications. In this study, we synthesized nitrogen-doped carbon dots (NCDs) via a straightforward one-step hydrothermal method. Subsequently, 3D flower-shaped CoHS@NCDs electrocatalysts were prepared by the integration of NCDs and cobalt hydroxide nanosheets (CoHS) using a solvothermal method. The resulting CoHS@NCDs electrocatalysts demonstrated outstanding catalytic performance for OER under alkaline conditions. Specifically, the CoHS@NCDs-3 electrocatalyst exhibited an overpotential of 280 mV at 10 mA cm−2(314 mV at 50 mA cm−2), representing an 80 mV improvement compared to CoHS, along with remarkable durability. Through comprehensive characterization, we revealed that the incorporation of NCDs facilitated the creation of numerous exposed active sites on CoHS, forming a unique electron transfer pathway (Co-N), thereby optimizing the kinetics of the OER reaction. This study underscored the significant potential of constructing electrocatalysts with exceptional OER activity based on transition metal hydroxides.
高效的电催化材料是提高析氧反应(OER)效率的关键。在这项研究中,我们通过简单的一步水热法合成了氮掺杂碳点(NCDs)。随后,采用溶剂热法制备了NCDs和氢氧化钴纳米片(CoHS)的三维花状CoHS@NCDs电催化剂。所得CoHS@NCDs电催化剂在碱性条件下对OER表现出优异的催化性能。具体来说,CoHS@NCDs-3电催化剂在10 mA cm - 2时的过电位为280 mV (50 mA cm - 2时为314 mV),与CoHS相比提高了80 mV,并且具有显著的耐用性。通过综合表征,我们发现NCDs的加入促进了CoHS上大量暴露活性位点的产生,形成了独特的电子转移途径(Co-N),从而优化了OER反应的动力学。该研究强调了基于过渡金属氢氧化物构建具有特殊OER活性的电催化剂的巨大潜力。
期刊介绍:
The Journal of Electroanalytical Chemistry is the foremost international journal devoted to the interdisciplinary subject of electrochemistry in all its aspects, theoretical as well as applied.
Electrochemistry is a wide ranging area that is in a state of continuous evolution. Rather than compiling a long list of topics covered by the Journal, the editors would like to draw particular attention to the key issues of novelty, topicality and quality. Papers should present new and interesting electrochemical science in a way that is accessible to the reader. The presentation and discussion should be at a level that is consistent with the international status of the Journal. Reports describing the application of well-established techniques to problems that are essentially technical will not be accepted. Similarly, papers that report observations but fail to provide adequate interpretation will be rejected by the Editors. Papers dealing with technical electrochemistry should be submitted to other specialist journals unless the authors can show that their work provides substantially new insights into electrochemical processes.