{"title":"构建用于增强氧进化反应的 NiFe/MnNiCo-LDH 异质结构,实现高效水分离","authors":"","doi":"10.1016/j.ijhydene.2024.09.114","DOIUrl":null,"url":null,"abstract":"<div><p>Developing highly efficient and cost-effective oxygen evolution reaction (OER) catalysts is pivotal for advancing sustainable energy storage and conversion technologies. Herein, NiFe/MnNiCo-LDH was successfully prepared by in-situ growth method. The OER performance of this composite material had been significantly enhanced through bimetallic atom modification and cation doping strategies. These modifications not only enhanced the electronic conductivity but also regulated the electron distribution within the catalyst structure. As a result, NiFe/MnNiCo-LDH can reach a current density of 10 mA cm<sup>−2</sup> at an overpotential of only 227 mV in the OER reaction. Moreover, the catalyst exhibited remarkable durability and maintained its high performance over an extended period of 48 h during the water splitting reaction. In this work, the potential of dual modification methods for optimizing catalytic properties of OER materials was investigated.</p></div>","PeriodicalId":337,"journal":{"name":"International Journal of Hydrogen Energy","volume":null,"pages":null},"PeriodicalIF":8.1000,"publicationDate":"2024-09-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Construction of NiFe/MnNiCo-LDH heterostructure for enhanced oxygen evolution reaction for efficient water splitting\",\"authors\":\"\",\"doi\":\"10.1016/j.ijhydene.2024.09.114\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Developing highly efficient and cost-effective oxygen evolution reaction (OER) catalysts is pivotal for advancing sustainable energy storage and conversion technologies. Herein, NiFe/MnNiCo-LDH was successfully prepared by in-situ growth method. The OER performance of this composite material had been significantly enhanced through bimetallic atom modification and cation doping strategies. These modifications not only enhanced the electronic conductivity but also regulated the electron distribution within the catalyst structure. As a result, NiFe/MnNiCo-LDH can reach a current density of 10 mA cm<sup>−2</sup> at an overpotential of only 227 mV in the OER reaction. Moreover, the catalyst exhibited remarkable durability and maintained its high performance over an extended period of 48 h during the water splitting reaction. In this work, the potential of dual modification methods for optimizing catalytic properties of OER materials was investigated.</p></div>\",\"PeriodicalId\":337,\"journal\":{\"name\":\"International Journal of Hydrogen Energy\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":8.1000,\"publicationDate\":\"2024-09-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Hydrogen Energy\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0360319924038230\",\"RegionNum\":2,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Hydrogen Energy","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0360319924038230","RegionNum":2,"RegionCategory":"工程技术","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
开发高效且具有成本效益的氧进化反应(OER)催化剂对于推进可持续能源储存和转换技术至关重要。本文采用原位生长法成功制备了镍铁/锰镍碳-LDH。通过双金属元素修饰和阳离子掺杂策略,这种复合材料的 OER 性能得到了显著提高。这些修饰不仅增强了电子导电性,还调节了催化剂结构内的电子分布。因此,NiFe/MnNiCo-LDH 在 OER 反应中的过电位仅为 227 mV,电流密度可达 10 mA cm-2。此外,该催化剂还表现出卓越的耐久性,在水分离反应中能在 48 小时内保持高性能。这项工作研究了双重改性方法在优化 OER 材料催化性能方面的潜力。
Construction of NiFe/MnNiCo-LDH heterostructure for enhanced oxygen evolution reaction for efficient water splitting
Developing highly efficient and cost-effective oxygen evolution reaction (OER) catalysts is pivotal for advancing sustainable energy storage and conversion technologies. Herein, NiFe/MnNiCo-LDH was successfully prepared by in-situ growth method. The OER performance of this composite material had been significantly enhanced through bimetallic atom modification and cation doping strategies. These modifications not only enhanced the electronic conductivity but also regulated the electron distribution within the catalyst structure. As a result, NiFe/MnNiCo-LDH can reach a current density of 10 mA cm−2 at an overpotential of only 227 mV in the OER reaction. Moreover, the catalyst exhibited remarkable durability and maintained its high performance over an extended period of 48 h during the water splitting reaction. In this work, the potential of dual modification methods for optimizing catalytic properties of OER materials was investigated.
期刊介绍:
The objective of the International Journal of Hydrogen Energy is to facilitate the exchange of new ideas, technological advancements, and research findings in the field of Hydrogen Energy among scientists and engineers worldwide. This journal showcases original research, both analytical and experimental, covering various aspects of Hydrogen Energy. These include production, storage, transmission, utilization, enabling technologies, environmental impact, economic considerations, and global perspectives on hydrogen and its carriers such as NH3, CH4, alcohols, etc.
The utilization aspect encompasses various methods such as thermochemical (combustion), photochemical, electrochemical (fuel cells), and nuclear conversion of hydrogen, hydrogen isotopes, and hydrogen carriers into thermal, mechanical, and electrical energies. The applications of these energies can be found in transportation (including aerospace), industrial, commercial, and residential sectors.