Self-Sacrificial Template-Induced Fabrication of Sustainable Diode-Type Micro-Junction toward Supercapacitors and Green H2 Evolution

IF 6.5 3区 材料科学 Q2 GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY
Upali Aparajita Mohanty, Ritik Mohanty, Kulamani Parida
{"title":"Self-Sacrificial Template-Induced Fabrication of Sustainable Diode-Type Micro-Junction toward Supercapacitors and Green H2 Evolution","authors":"Upali Aparajita Mohanty,&nbsp;Ritik Mohanty,&nbsp;Kulamani Parida","doi":"10.1002/adsu.202400858","DOIUrl":null,"url":null,"abstract":"<p>Energy conversion and storage are the key challenges in green chemistry that have garnered significant attention in recent decades. Heterostructure materials, with their unique interfaces, robust architectures, and synergistic effects, show great promise in enhancing energy conversion and storage capabilities. However, the intricate relationship between their structural properties and performance requires further investigation. This study introduces a novel diode-type interfacial micro-junction fabricated from FeCo-based layered double hydroxide (LDH) using a self-sacrificial template-induced method. The micro-junction structure significantly enhances the material's electronic properties, enabling efficient charge separation and ion transport. As a result, the material demonstrates remarkable performance in both photocatalytic hydrogen evolution and supercapacitor applications. Specifically, the optimized material exhibits superior specific capacitance (1814.14 F g<sup>−1</sup> at 1 A g<sup>−1</sup>), high energy density (61.6 Wh kg<sup>−1</sup>), and excellent cycling stability (90.7% capacitance retention after 15 000 cycles) in coin cell supercapacitors. Additionally, the material's unique light-harvesting capabilities and enhanced charge-carrier dynamics make it a promising candidate for photocatalytic H<sub>2</sub> evolution at a rate of 577.8 µmol h<sup>−1</sup>. This work not only advances the development of multifunctional materials for clean energy applications, but also opens new avenues for the design of high-performance energy storage and conversion technologies.</p>","PeriodicalId":7294,"journal":{"name":"Advanced Sustainable Systems","volume":"9 4","pages":""},"PeriodicalIF":6.5000,"publicationDate":"2025-02-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Sustainable Systems","FirstCategoryId":"88","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/adsu.202400858","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Energy conversion and storage are the key challenges in green chemistry that have garnered significant attention in recent decades. Heterostructure materials, with their unique interfaces, robust architectures, and synergistic effects, show great promise in enhancing energy conversion and storage capabilities. However, the intricate relationship between their structural properties and performance requires further investigation. This study introduces a novel diode-type interfacial micro-junction fabricated from FeCo-based layered double hydroxide (LDH) using a self-sacrificial template-induced method. The micro-junction structure significantly enhances the material's electronic properties, enabling efficient charge separation and ion transport. As a result, the material demonstrates remarkable performance in both photocatalytic hydrogen evolution and supercapacitor applications. Specifically, the optimized material exhibits superior specific capacitance (1814.14 F g−1 at 1 A g−1), high energy density (61.6 Wh kg−1), and excellent cycling stability (90.7% capacitance retention after 15 000 cycles) in coin cell supercapacitors. Additionally, the material's unique light-harvesting capabilities and enhanced charge-carrier dynamics make it a promising candidate for photocatalytic H2 evolution at a rate of 577.8 µmol h−1. This work not only advances the development of multifunctional materials for clean energy applications, but also opens new avenues for the design of high-performance energy storage and conversion technologies.

Abstract Image

面向超级电容器的可持续二极管型微结的自我牺牲模板诱导制造与绿色H2演化
能量转换和储存是绿色化学的关键挑战,近几十年来引起了人们的极大关注。异质结构材料以其独特的界面、坚固的结构和协同效应,在增强能量转换和存储能力方面显示出巨大的希望。然而,它们的结构特性和性能之间的复杂关系需要进一步研究。本文介绍了一种新型的二极管型界面微结,该微结是由基于feo的层状双氢氧化物(LDH)采用自我牺牲模板诱导方法制备的。微结结构显著提高了材料的电子性能,实现了有效的电荷分离和离子传输。结果表明,该材料在光催化析氢和超级电容器应用中表现出卓越的性能。具体而言,优化后的材料在纽扣电池超级电容器中表现出优异的比电容(在1 A g−1时为1814.14 F g−1)、高能量密度(61.6 Wh kg−1)和优异的循环稳定性(循环15000次后电容保持率为90.7%)。此外,该材料独特的光捕获能力和增强的电荷载流子动力学使其成为光催化H2演化的有希望的候选者,其速率为577.8µmol h−1。这项工作不仅推动了清洁能源应用多功能材料的发展,而且为高性能储能和转换技术的设计开辟了新的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Advanced Sustainable Systems
Advanced Sustainable Systems Environmental Science-General Environmental Science
CiteScore
10.80
自引率
4.20%
发文量
186
期刊介绍: Advanced Sustainable Systems, a part of the esteemed Advanced portfolio, serves as an interdisciplinary sustainability science journal. It focuses on impactful research in the advancement of sustainable, efficient, and less wasteful systems and technologies. Aligned with the UN's Sustainable Development Goals, the journal bridges knowledge gaps between fundamental research, implementation, and policy-making. Covering diverse topics such as climate change, food sustainability, environmental science, renewable energy, water, urban development, and socio-economic challenges, it contributes to the understanding and promotion of sustainable systems.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信