{"title":"嵌入碳点的钴镍双金属磷化物纳米棒作为整体水分离的高效电催化剂","authors":"Yantong Long, Guoliang Zhao, Liuxin Yang, Yongjun Xu and Chen Xu","doi":"10.1039/D4TA04340E","DOIUrl":null,"url":null,"abstract":"<p >Efficient bifunctional catalysts for hydrogen/oxygen evolution reactions (HER/OER) are critical for industrial application of overall water splitting. Herein, a self-supported nanostructure consisting of CoNi–P and embedded carbon dots (denoted as CoNi–P/CDs/NF) with large specific surface area has been designed and fabricated, through a phosphorization process on precursors grown on 3D porous Ni foam. The resultant electrocatalyst exhibited excellent electrocatalytic performance for both the HER (45.2 mV@10 mA cm<small><sup>−2</sup></small>) and OER (184.8 mV@20 mA cm<small><sup>−2</sup></small>) under alkaline conditions. The cell voltage of the full water splitting device assembled was only 1.50 V to achieve 20 mA cm<small><sup>−2</sup></small> and exhibited great durability benefiting from the self-supported nanostructure. The density functional theory (DFT) calculations and XPS analysis suggest that the synergistic coupling effect between CDs and substrate CoNi–P could tune the electronic structure. Moreover, the embedded CDs increase electrical conductivity and active sites of the catalyst. Both of these and the high specific surface benefited from the 1D/3D hierarchical structure could explain the excellent electrocatalytic performance. The rational materials design of 1D/3D hierarchical structured non-noble bimetallic phosphide catalysts in this work may suggest a new strategy for designing bifunctional electrocatalysts.</p>","PeriodicalId":82,"journal":{"name":"Journal of Materials Chemistry A","volume":" 47","pages":" 33301-33313"},"PeriodicalIF":9.5000,"publicationDate":"2024-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Carbon dot embedded CoNi bimetallic phosphide nanorods as an efficient electrocatalyst for overall water splitting†\",\"authors\":\"Yantong Long, Guoliang Zhao, Liuxin Yang, Yongjun Xu and Chen Xu\",\"doi\":\"10.1039/D4TA04340E\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Efficient bifunctional catalysts for hydrogen/oxygen evolution reactions (HER/OER) are critical for industrial application of overall water splitting. Herein, a self-supported nanostructure consisting of CoNi–P and embedded carbon dots (denoted as CoNi–P/CDs/NF) with large specific surface area has been designed and fabricated, through a phosphorization process on precursors grown on 3D porous Ni foam. The resultant electrocatalyst exhibited excellent electrocatalytic performance for both the HER (45.2 mV@10 mA cm<small><sup>−2</sup></small>) and OER (184.8 mV@20 mA cm<small><sup>−2</sup></small>) under alkaline conditions. The cell voltage of the full water splitting device assembled was only 1.50 V to achieve 20 mA cm<small><sup>−2</sup></small> and exhibited great durability benefiting from the self-supported nanostructure. The density functional theory (DFT) calculations and XPS analysis suggest that the synergistic coupling effect between CDs and substrate CoNi–P could tune the electronic structure. Moreover, the embedded CDs increase electrical conductivity and active sites of the catalyst. Both of these and the high specific surface benefited from the 1D/3D hierarchical structure could explain the excellent electrocatalytic performance. The rational materials design of 1D/3D hierarchical structured non-noble bimetallic phosphide catalysts in this work may suggest a new strategy for designing bifunctional electrocatalysts.</p>\",\"PeriodicalId\":82,\"journal\":{\"name\":\"Journal of Materials Chemistry A\",\"volume\":\" 47\",\"pages\":\" 33301-33313\"},\"PeriodicalIF\":9.5000,\"publicationDate\":\"2024-10-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Materials Chemistry A\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2024/ta/d4ta04340e\",\"RegionNum\":2,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Materials Chemistry A","FirstCategoryId":"88","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/ta/d4ta04340e","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
摘要
用于氢/氧进化反应(HER/OER)的高效双功能催化剂对于整体水分离的工业应用至关重要。在此,通过对生长在三维多孔镍泡沫上的前驱体进行磷化处理,设计并制造了一种由 CoNi-P 和嵌入式碳点(称为 CoNi-P/CDs/NF )组成的具有大比表面积的自支撑纳米结构。所制备的电催化剂在碱性条件下对 HER(45.2 mV@10 mA cm-2)和 OER(184.8 mV@20 mA cm-2)均表现出优异的电催化性能。组装好的全水分离装置的电池电压仅为 1.50 V,就能达到 20 mA cm-2,并且得益于自支撑纳米结构,表现出极高的耐用性。密度函数理论(DFT)计算和 XPS 分析表明,CD 与基底 CoNi-P 之间的协同耦合效应可以调整电子结构。此外,嵌入的 CD 增加了催化剂的导电性和活性位点。这两点以及一维/三维分层结构带来的高比表面,都是催化剂具有优异电催化性能的原因。这项工作中对 1D/3D 分层结构非贵金属双金属磷化物催化剂的合理材料设计可能为设计双功能电催化剂提供了一种新策略。
Carbon dot embedded CoNi bimetallic phosphide nanorods as an efficient electrocatalyst for overall water splitting†
Efficient bifunctional catalysts for hydrogen/oxygen evolution reactions (HER/OER) are critical for industrial application of overall water splitting. Herein, a self-supported nanostructure consisting of CoNi–P and embedded carbon dots (denoted as CoNi–P/CDs/NF) with large specific surface area has been designed and fabricated, through a phosphorization process on precursors grown on 3D porous Ni foam. The resultant electrocatalyst exhibited excellent electrocatalytic performance for both the HER (45.2 mV@10 mA cm−2) and OER (184.8 mV@20 mA cm−2) under alkaline conditions. The cell voltage of the full water splitting device assembled was only 1.50 V to achieve 20 mA cm−2 and exhibited great durability benefiting from the self-supported nanostructure. The density functional theory (DFT) calculations and XPS analysis suggest that the synergistic coupling effect between CDs and substrate CoNi–P could tune the electronic structure. Moreover, the embedded CDs increase electrical conductivity and active sites of the catalyst. Both of these and the high specific surface benefited from the 1D/3D hierarchical structure could explain the excellent electrocatalytic performance. The rational materials design of 1D/3D hierarchical structured non-noble bimetallic phosphide catalysts in this work may suggest a new strategy for designing bifunctional electrocatalysts.
期刊介绍:
The Journal of Materials Chemistry A, B & C covers a wide range of high-quality studies in the field of materials chemistry, with each section focusing on specific applications of the materials studied. Journal of Materials Chemistry A emphasizes applications in energy and sustainability, including topics such as artificial photosynthesis, batteries, and fuel cells. Journal of Materials Chemistry B focuses on applications in biology and medicine, while Journal of Materials Chemistry C covers applications in optical, magnetic, and electronic devices. Example topic areas within the scope of Journal of Materials Chemistry A include catalysis, green/sustainable materials, sensors, and water treatment, among others.