Wancheng Zhao , Jiapeng Ma , Dong Tian , Baotao Kang , Fangquan Xia , Jing Cheng , Yajun Wu , Mengyao Wang , Gang Wu
{"title":"集成了多功能碳纳米管和 Ni-Ni(OH)2 异质结构的自支撑薄膜催化剂用于促进氢气进化","authors":"Wancheng Zhao , Jiapeng Ma , Dong Tian , Baotao Kang , Fangquan Xia , Jing Cheng , Yajun Wu , Mengyao Wang , Gang Wu","doi":"10.1016/S1872-2067(24)60057-4","DOIUrl":null,"url":null,"abstract":"<div><p>In order to reduce energy consumption in water electrolysis, it is of great importance to design active and stable electrocatalysts for hydrogen evolution reaction (HER) in alkaline solution, especially based on earth-abundant metal. Here we integrate carbon nanotubes (CNTs) and Ni-Ni(OH)<sub>2</sub> heterostructure multifunctional components to design a self-supported 3D CNTs-Ni-Ni(OH)<sub>2</sub> catalyst for HER by composite deposition and subsequent <em>in-situ</em> oxidation. In alkaline solution, this designed CNTs-Ni-Ni(OH)<sub>2</sub> catalyst exhibits 0 mV onset overpotential, and overpotentials of 65 mV and 109 mV at 10 and 50 mA/cm<sup>2</sup> respectively. Electrochemical measurements, characterizations, and simulation results attribute the outstanding performance to the incorporation of CNTs and heterostructure. CNTs induce the formation 3D catalytic surface, enhance electrochemical active surface area, and more importantly weaken the adsorption of H. Moreover, the formation of heterostructure, especially reversible Ni(OH)<sub>2</sub>, supplies active sites and adjusts the adsorption strength of H atom to an optimal value. CNTs and heterostructure synergistically facilitate water adsorption, promote water dissociation, and accelerate H<sub>2</sub> desorption. Significantly, integration of multifunctional components supplies a distinct strategy for development of cost-effective electrocatalyst with outstanding performance.</p></div>","PeriodicalId":9832,"journal":{"name":"Chinese Journal of Catalysis","volume":"62 ","pages":"Pages 287-295"},"PeriodicalIF":15.7000,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Self-supported film catalyst integrated with multifunctional carbon nanotubes and Ni-Ni(OH)2 heterostructure for promoted hydrogen evolution\",\"authors\":\"Wancheng Zhao , Jiapeng Ma , Dong Tian , Baotao Kang , Fangquan Xia , Jing Cheng , Yajun Wu , Mengyao Wang , Gang Wu\",\"doi\":\"10.1016/S1872-2067(24)60057-4\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>In order to reduce energy consumption in water electrolysis, it is of great importance to design active and stable electrocatalysts for hydrogen evolution reaction (HER) in alkaline solution, especially based on earth-abundant metal. Here we integrate carbon nanotubes (CNTs) and Ni-Ni(OH)<sub>2</sub> heterostructure multifunctional components to design a self-supported 3D CNTs-Ni-Ni(OH)<sub>2</sub> catalyst for HER by composite deposition and subsequent <em>in-situ</em> oxidation. In alkaline solution, this designed CNTs-Ni-Ni(OH)<sub>2</sub> catalyst exhibits 0 mV onset overpotential, and overpotentials of 65 mV and 109 mV at 10 and 50 mA/cm<sup>2</sup> respectively. Electrochemical measurements, characterizations, and simulation results attribute the outstanding performance to the incorporation of CNTs and heterostructure. CNTs induce the formation 3D catalytic surface, enhance electrochemical active surface area, and more importantly weaken the adsorption of H. Moreover, the formation of heterostructure, especially reversible Ni(OH)<sub>2</sub>, supplies active sites and adjusts the adsorption strength of H atom to an optimal value. CNTs and heterostructure synergistically facilitate water adsorption, promote water dissociation, and accelerate H<sub>2</sub> desorption. Significantly, integration of multifunctional components supplies a distinct strategy for development of cost-effective electrocatalyst with outstanding performance.</p></div>\",\"PeriodicalId\":9832,\"journal\":{\"name\":\"Chinese Journal of Catalysis\",\"volume\":\"62 \",\"pages\":\"Pages 287-295\"},\"PeriodicalIF\":15.7000,\"publicationDate\":\"2024-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chinese Journal of Catalysis\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1872206724600574\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, APPLIED\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chinese Journal of Catalysis","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1872206724600574","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
Self-supported film catalyst integrated with multifunctional carbon nanotubes and Ni-Ni(OH)2 heterostructure for promoted hydrogen evolution
In order to reduce energy consumption in water electrolysis, it is of great importance to design active and stable electrocatalysts for hydrogen evolution reaction (HER) in alkaline solution, especially based on earth-abundant metal. Here we integrate carbon nanotubes (CNTs) and Ni-Ni(OH)2 heterostructure multifunctional components to design a self-supported 3D CNTs-Ni-Ni(OH)2 catalyst for HER by composite deposition and subsequent in-situ oxidation. In alkaline solution, this designed CNTs-Ni-Ni(OH)2 catalyst exhibits 0 mV onset overpotential, and overpotentials of 65 mV and 109 mV at 10 and 50 mA/cm2 respectively. Electrochemical measurements, characterizations, and simulation results attribute the outstanding performance to the incorporation of CNTs and heterostructure. CNTs induce the formation 3D catalytic surface, enhance electrochemical active surface area, and more importantly weaken the adsorption of H. Moreover, the formation of heterostructure, especially reversible Ni(OH)2, supplies active sites and adjusts the adsorption strength of H atom to an optimal value. CNTs and heterostructure synergistically facilitate water adsorption, promote water dissociation, and accelerate H2 desorption. Significantly, integration of multifunctional components supplies a distinct strategy for development of cost-effective electrocatalyst with outstanding performance.
期刊介绍:
The journal covers a broad scope, encompassing new trends in catalysis for applications in energy production, environmental protection, and the preparation of materials, petroleum chemicals, and fine chemicals. It explores the scientific foundation for preparing and activating catalysts of commercial interest, emphasizing representative models.The focus includes spectroscopic methods for structural characterization, especially in situ techniques, as well as new theoretical methods with practical impact in catalysis and catalytic reactions.The journal delves into the relationship between homogeneous and heterogeneous catalysis and includes theoretical studies on the structure and reactivity of catalysts.Additionally, contributions on photocatalysis, biocatalysis, surface science, and catalysis-related chemical kinetics are welcomed.