氮化石墨碳支撑的 MnO2 纳米粒子作为氧气还原和进化的电催化剂

IF 2.7 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Aušrinė Zabielaitė, Virginija Kepenienė, Dijana Šimkūnaitė, Raminta Stagniūnaitė, Vitalija Jasulaitienė, Giedrius Stalnionis, Jūratė Vaičiūnienė, Loreta Tamašauskaitė-Tamašiūnaitė and Eugenijus Norkus
{"title":"氮化石墨碳支撑的 MnO2 纳米粒子作为氧气还原和进化的电催化剂","authors":"Aušrinė Zabielaitė, Virginija Kepenienė, Dijana Šimkūnaitė, Raminta Stagniūnaitė, Vitalija Jasulaitienė, Giedrius Stalnionis, Jūratė Vaičiūnienė, Loreta Tamašauskaitė-Tamašiūnaitė and Eugenijus Norkus","doi":"10.1039/D4NJ03407D","DOIUrl":null,"url":null,"abstract":"<p >The aim of this study is to present a straightforward methodology for the preparation of non-precious metal catalysts comprising MnO<small><sub>2</sub></small> and carbonaceous materials, namely graphite powder (C), graphitic carbon nitride (gCN), and graphitic carbon nitride/graphite powder (gCN/C) substrates. The morphology and composition of the prepared MnO<small><sub>2</sub></small>/C, MnO<small><sub>2</sub></small>–gCN, and MnO<small><sub>2</sub></small>–gCN/C catalysts have been investigated using X-ray diffraction (XRD), field-emission scanning electron microscopy (FE-SEM), X-ray photoelectron spectroscopy (XPS), and inductively coupled plasma optical emission spectroscopy (ICP-OES). The electrochemical performance of the prepared MnO<small><sub>2</sub></small>/C, MnO<small><sub>2</sub></small>–gCN, and MnO<small><sub>2</sub></small>–gCN/C catalysts has been investigated for the oxygen reduction reaction (ORR) and oxygen evolution (OER) reaction using cyclic and linear voltammetry. All of the investigated catalysts exhibited enhanced electrocatalytic activity with regard to the ORR and OER processes when compared with the bare substrates. The MnO<small><sub>2</sub></small>–gCN/C catalyst was found to be the most efficient catalyst for both investigated reactions when compared with MnO<small><sub>2</sub></small>/C and MnO<small><sub>2</sub></small>–gCN. The MnO<small><sub>2</sub></small>–gCN/C catalyst demonstrated the most positive ORR onset potential of 0.9 V and the most negative OER onset potential of 1.53 V. Furthermore, it demonstrated remarkable stability, retaining approximately 85% of its initial signal after a continuous test of 24 hours in both long-term ORR and OER processes.</p>","PeriodicalId":95,"journal":{"name":"New Journal of Chemistry","volume":" 46","pages":" 19389-19402"},"PeriodicalIF":2.7000,"publicationDate":"2024-11-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"MnO2 nanoparticles supported on graphitic carbon nitride as an electrocatalyst for oxygen reduction and evolution\",\"authors\":\"Aušrinė Zabielaitė, Virginija Kepenienė, Dijana Šimkūnaitė, Raminta Stagniūnaitė, Vitalija Jasulaitienė, Giedrius Stalnionis, Jūratė Vaičiūnienė, Loreta Tamašauskaitė-Tamašiūnaitė and Eugenijus Norkus\",\"doi\":\"10.1039/D4NJ03407D\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >The aim of this study is to present a straightforward methodology for the preparation of non-precious metal catalysts comprising MnO<small><sub>2</sub></small> and carbonaceous materials, namely graphite powder (C), graphitic carbon nitride (gCN), and graphitic carbon nitride/graphite powder (gCN/C) substrates. The morphology and composition of the prepared MnO<small><sub>2</sub></small>/C, MnO<small><sub>2</sub></small>–gCN, and MnO<small><sub>2</sub></small>–gCN/C catalysts have been investigated using X-ray diffraction (XRD), field-emission scanning electron microscopy (FE-SEM), X-ray photoelectron spectroscopy (XPS), and inductively coupled plasma optical emission spectroscopy (ICP-OES). The electrochemical performance of the prepared MnO<small><sub>2</sub></small>/C, MnO<small><sub>2</sub></small>–gCN, and MnO<small><sub>2</sub></small>–gCN/C catalysts has been investigated for the oxygen reduction reaction (ORR) and oxygen evolution (OER) reaction using cyclic and linear voltammetry. All of the investigated catalysts exhibited enhanced electrocatalytic activity with regard to the ORR and OER processes when compared with the bare substrates. The MnO<small><sub>2</sub></small>–gCN/C catalyst was found to be the most efficient catalyst for both investigated reactions when compared with MnO<small><sub>2</sub></small>/C and MnO<small><sub>2</sub></small>–gCN. The MnO<small><sub>2</sub></small>–gCN/C catalyst demonstrated the most positive ORR onset potential of 0.9 V and the most negative OER onset potential of 1.53 V. Furthermore, it demonstrated remarkable stability, retaining approximately 85% of its initial signal after a continuous test of 24 hours in both long-term ORR and OER processes.</p>\",\"PeriodicalId\":95,\"journal\":{\"name\":\"New Journal of Chemistry\",\"volume\":\" 46\",\"pages\":\" 19389-19402\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2024-11-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"New Journal of Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2024/nj/d4nj03407d\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"New Journal of Chemistry","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/nj/d4nj03407d","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

摘要

本研究旨在提出一种简单直接的方法,用于制备由二氧化锰和碳质材料(即石墨粉 (C)、氮化石墨碳 (gCN) 和氮化石墨碳/石墨粉 (gCN/C) 基质)组成的非贵金属催化剂。利用 X 射线衍射 (XRD)、场发射扫描电子显微镜 (FE-SEM)、X 射线光电子能谱 (XPS) 和电感耦合等离子体光发射光谱 (ICP-OES) 研究了制备的 MnO2/C、MnO2-gCN 和 MnO2-gCN/C 催化剂的形态和组成。利用循环和线性伏安法研究了制备的 MnO2/C、MnO2-gCN 和 MnO2-gCN/C 催化剂在氧还原反应(ORR)和氧进化反应(OER)中的电化学性能。与裸基底相比,所有被研究的催化剂在 ORR 和 OER 过程中都表现出更强的电催化活性。与 MnO2/C 和 MnO2-gCN 相比,MnO2-gCN/C 催化剂是两个研究反应中最有效的催化剂。MnO2-gCN/C 催化剂的正 ORR 起始电位最高,为 0.9 V,负 OER 起始电位最高,为 1.53 V。此外,该催化剂还表现出卓越的稳定性,在长期 ORR 和 OER 过程中连续测试 24 小时后,仍能保持约 85% 的初始信号。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

MnO2 nanoparticles supported on graphitic carbon nitride as an electrocatalyst for oxygen reduction and evolution

MnO2 nanoparticles supported on graphitic carbon nitride as an electrocatalyst for oxygen reduction and evolution

The aim of this study is to present a straightforward methodology for the preparation of non-precious metal catalysts comprising MnO2 and carbonaceous materials, namely graphite powder (C), graphitic carbon nitride (gCN), and graphitic carbon nitride/graphite powder (gCN/C) substrates. The morphology and composition of the prepared MnO2/C, MnO2–gCN, and MnO2–gCN/C catalysts have been investigated using X-ray diffraction (XRD), field-emission scanning electron microscopy (FE-SEM), X-ray photoelectron spectroscopy (XPS), and inductively coupled plasma optical emission spectroscopy (ICP-OES). The electrochemical performance of the prepared MnO2/C, MnO2–gCN, and MnO2–gCN/C catalysts has been investigated for the oxygen reduction reaction (ORR) and oxygen evolution (OER) reaction using cyclic and linear voltammetry. All of the investigated catalysts exhibited enhanced electrocatalytic activity with regard to the ORR and OER processes when compared with the bare substrates. The MnO2–gCN/C catalyst was found to be the most efficient catalyst for both investigated reactions when compared with MnO2/C and MnO2–gCN. The MnO2–gCN/C catalyst demonstrated the most positive ORR onset potential of 0.9 V and the most negative OER onset potential of 1.53 V. Furthermore, it demonstrated remarkable stability, retaining approximately 85% of its initial signal after a continuous test of 24 hours in both long-term ORR and OER processes.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
New Journal of Chemistry
New Journal of Chemistry 化学-化学综合
CiteScore
5.30
自引率
6.10%
发文量
1832
审稿时长
2 months
期刊介绍: A journal for new directions in chemistry
×
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