Plasma induced Fe-NX active sites to improve the oxygen reduction reaction performance

Peng Rao , Tian-Jiao Wang , Jing Li , Pei-Lin Deng , Yi-Jun Shen , Yu Chen , Xin-Long Tian
{"title":"Plasma induced Fe-NX active sites to improve the oxygen reduction reaction performance","authors":"Peng Rao ,&nbsp;Tian-Jiao Wang ,&nbsp;Jing Li ,&nbsp;Pei-Lin Deng ,&nbsp;Yi-Jun Shen ,&nbsp;Yu Chen ,&nbsp;Xin-Long Tian","doi":"10.1016/j.asems.2022.100005","DOIUrl":null,"url":null,"abstract":"<div><p>Rational design of high-efficient and low-cost catalysts as alternatives to Pt-based catalysts toward the oxygen reduction reaction (ORR) is extremely desirable but challenging. In this work, Fe@NCNT is firstly synthesized via the one-pot pyrolysis method, then Fe-N<sub><em>X</em></sub> active species are <em>in-situ</em> created on the prepared Fe@NCNT by a feasible “plasma inducing” strategy to synthesize the resulting catalyst (Fe@NCNT-P) for ORR. The morphology of Fe@NCNT-P is perfectly inherited by the derived carbon precursor, resulting in the core-shell structure of carbon-coated Fe and a mesoporous dominant nanostructure with a high specific surface area of 536 m<sup>2</sup> g<sup>−1</sup>. The resultant Fe@NCNT-P catalyst exhibits remarkable ORR activity and durability, as well as outstanding performance in assembled zinc-air battery (ZAB) test with a peak power density of 240 mW cm<sup>−2</sup>. This work not only reports a novel and robust ORR catalyst, but also proposes a simple and effective strategy to improve the ORR electrocatalytic performance.</p></div>","PeriodicalId":100036,"journal":{"name":"Advanced Sensor and Energy Materials","volume":"1 1","pages":"Article 100005"},"PeriodicalIF":0.0000,"publicationDate":"2022-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2773045X2200005X/pdfft?md5=f54efd5266ecc524502600d42e344a4b&pid=1-s2.0-S2773045X2200005X-main.pdf","citationCount":"28","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Sensor and Energy Materials","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2773045X2200005X","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 28

Abstract

Rational design of high-efficient and low-cost catalysts as alternatives to Pt-based catalysts toward the oxygen reduction reaction (ORR) is extremely desirable but challenging. In this work, Fe@NCNT is firstly synthesized via the one-pot pyrolysis method, then Fe-NX active species are in-situ created on the prepared Fe@NCNT by a feasible “plasma inducing” strategy to synthesize the resulting catalyst (Fe@NCNT-P) for ORR. The morphology of Fe@NCNT-P is perfectly inherited by the derived carbon precursor, resulting in the core-shell structure of carbon-coated Fe and a mesoporous dominant nanostructure with a high specific surface area of 536 m2 g−1. The resultant Fe@NCNT-P catalyst exhibits remarkable ORR activity and durability, as well as outstanding performance in assembled zinc-air battery (ZAB) test with a peak power density of 240 mW cm−2. This work not only reports a novel and robust ORR catalyst, but also proposes a simple and effective strategy to improve the ORR electrocatalytic performance.

Abstract Image

等离子体诱导Fe-NX活性位点,提高氧还原反应性能
合理设计高效、低成本的催化剂替代pt基催化剂用于氧还原反应(ORR)是非常可取的,但也具有挑战性。本文首先采用一锅热解法合成Fe@NCNT,然后采用可行的“等离子体诱导”策略在制备好的Fe@NCNT上原位生成Fe-NX活性物质,合成ORR催化剂(Fe@NCNT-P)。Fe@NCNT-P的形貌被衍生的碳前驱体完美地继承,形成了碳包覆铁的核壳结构和具有536 m2 g−1的高比表面积的介孔优势纳米结构。所得Fe@NCNT-P催化剂表现出良好的ORR活性和耐久性,在组装锌-空气电池(ZAB)测试中表现优异,峰值功率密度为240 mW cm - 2。本工作不仅报道了一种新颖而坚固的ORR催化剂,而且提出了一种简单有效的提高ORR电催化性能的策略。
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
自引率
0.00%
发文量
0
×
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