Youtao Yao , Jiahui Lyu , Xingchuan Li , Cheng Chen , Francis Verpoort , John Wang , Zhenghui Pan , Zongkui Kou
{"title":"大电流密度下氧进化反应的高效电催化剂综述","authors":"Youtao Yao , Jiahui Lyu , Xingchuan Li , Cheng Chen , Francis Verpoort , John Wang , Zhenghui Pan , Zongkui Kou","doi":"10.1016/j.decarb.2024.100062","DOIUrl":null,"url":null,"abstract":"<div><p>Within the framework of achieving global carbon neutrality, utilizing electrocatalytic water splitting to produce “green hydrogen” holds significant promise as an effective solution. The strategic development of economic, efficient, and robust anode oxygen evolution reaction (OER) catalysts is one of the imminent bottlenecks for scalable application of electrolyzing water into hydrogen and oxygen, particularly under actual yet harsh operating conditions such as large current density (LCD). In this review, we intend to summarize the advances and challenges in the understanding of the electrocatalytic OER at LCD. Initially, the impact of LCD on the electron transfer, mass transportation efficiency and catalyst stability is identified and summarized. Furthermore, five basic principles for catalyst design, namely the dimension of the materials, surface chemistry, creation of electron transfer pathways, synergy among nano-, micro-, and macroscale structures, and catalyst-support interaction, are systematically discussed. Specifically, the correlation between the synergistic function of the multiscale structures and the catalyst-support interaction is highlighted to direct improvements in catalyst efficiency and durability at the LCD. Finally, an outlook is prospected to further our understanding of these topics and provide related researchers with potential research areas.</p></div>","PeriodicalId":100356,"journal":{"name":"DeCarbon","volume":"5 ","pages":"Article 100062"},"PeriodicalIF":0.0000,"publicationDate":"2024-07-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2949881324000283/pdfft?md5=c51e75994627075ff353fec18b844865&pid=1-s2.0-S2949881324000283-main.pdf","citationCount":"0","resultStr":"{\"title\":\"A review of efficient electrocatalysts for the oxygen evolution reaction at large current density\",\"authors\":\"Youtao Yao , Jiahui Lyu , Xingchuan Li , Cheng Chen , Francis Verpoort , John Wang , Zhenghui Pan , Zongkui Kou\",\"doi\":\"10.1016/j.decarb.2024.100062\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Within the framework of achieving global carbon neutrality, utilizing electrocatalytic water splitting to produce “green hydrogen” holds significant promise as an effective solution. The strategic development of economic, efficient, and robust anode oxygen evolution reaction (OER) catalysts is one of the imminent bottlenecks for scalable application of electrolyzing water into hydrogen and oxygen, particularly under actual yet harsh operating conditions such as large current density (LCD). In this review, we intend to summarize the advances and challenges in the understanding of the electrocatalytic OER at LCD. Initially, the impact of LCD on the electron transfer, mass transportation efficiency and catalyst stability is identified and summarized. Furthermore, five basic principles for catalyst design, namely the dimension of the materials, surface chemistry, creation of electron transfer pathways, synergy among nano-, micro-, and macroscale structures, and catalyst-support interaction, are systematically discussed. Specifically, the correlation between the synergistic function of the multiscale structures and the catalyst-support interaction is highlighted to direct improvements in catalyst efficiency and durability at the LCD. Finally, an outlook is prospected to further our understanding of these topics and provide related researchers with potential research areas.</p></div>\",\"PeriodicalId\":100356,\"journal\":{\"name\":\"DeCarbon\",\"volume\":\"5 \",\"pages\":\"Article 100062\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-07-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2949881324000283/pdfft?md5=c51e75994627075ff353fec18b844865&pid=1-s2.0-S2949881324000283-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"DeCarbon\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2949881324000283\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"DeCarbon","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2949881324000283","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
在实现全球碳中和的框架下,利用电催化水分离技术生产 "绿色氢气 "是大有可为的有效解决方案。战略性地开发经济、高效、坚固的阳极氧进化反应(OER)催化剂,是将水电解为氢气和氧气的规模化应用中迫在眉睫的瓶颈之一,尤其是在大电流密度(LCD)等实际而苛刻的操作条件下。在本综述中,我们将总结在了解 LCD 下电催化 OER 方面的进展和挑战。首先,我们确定并总结了 LCD 对电子传输、质量传输效率和催化剂稳定性的影响。此外,还系统地讨论了催化剂设计的五项基本原则,即材料尺寸、表面化学、电子传递途径的创建、纳米、微米和宏观结构之间的协同作用以及催化剂与支持物之间的相互作用。特别强调了多尺度结构的协同功能与催化剂与支撑物相互作用之间的相关性,以直接提高液晶显示器上催化剂的效率和耐用性。最后,展望了我们对这些主题的进一步理解,并为相关研究人员提供了潜在的研究领域。
A review of efficient electrocatalysts for the oxygen evolution reaction at large current density
Within the framework of achieving global carbon neutrality, utilizing electrocatalytic water splitting to produce “green hydrogen” holds significant promise as an effective solution. The strategic development of economic, efficient, and robust anode oxygen evolution reaction (OER) catalysts is one of the imminent bottlenecks for scalable application of electrolyzing water into hydrogen and oxygen, particularly under actual yet harsh operating conditions such as large current density (LCD). In this review, we intend to summarize the advances and challenges in the understanding of the electrocatalytic OER at LCD. Initially, the impact of LCD on the electron transfer, mass transportation efficiency and catalyst stability is identified and summarized. Furthermore, five basic principles for catalyst design, namely the dimension of the materials, surface chemistry, creation of electron transfer pathways, synergy among nano-, micro-, and macroscale structures, and catalyst-support interaction, are systematically discussed. Specifically, the correlation between the synergistic function of the multiscale structures and the catalyst-support interaction is highlighted to direct improvements in catalyst efficiency and durability at the LCD. Finally, an outlook is prospected to further our understanding of these topics and provide related researchers with potential research areas.