在银和铜装饰的纳米碳片上选择性地将 CO2 电还原成 CO

IF 3.2 Q2 CHEMISTRY, PHYSICAL Energy advances Pub Date : 2024-08-06 DOI:10.1039/D4YA00462K
Ahmad Faraz, Waheed Iqbal, Shayan Gul, Fehmida K. Kanodarwala, Muhammad Nadeem Zafar, Guobao Xu and Muhammad Arif Nadeem
{"title":"在银和铜装饰的纳米碳片上选择性地将 CO2 电还原成 CO","authors":"Ahmad Faraz, Waheed Iqbal, Shayan Gul, Fehmida K. Kanodarwala, Muhammad Nadeem Zafar, Guobao Xu and Muhammad Arif Nadeem","doi":"10.1039/D4YA00462K","DOIUrl":null,"url":null,"abstract":"<p >The electrocatalytic CO<small><sub>2</sub></small> reduction reaction (eCO<small><sub>2</sub></small>RR) has the potential to effectively cut carbon emission. However, the activity and selectivity of eCO<small><sub>2</sub></small>RR catalysts are topical due to the intricacy of the reaction components and mechanism. Herein, we have decorated silver and copper nanoparticles over carbon nanoflakes to achieve an Ag–Cu NPs/C system that enables selective reduction of CO<small><sub>2</sub></small> into CO. The catalyst is prepared by incorporating Ag nanoparticles into a Cu-BTC MOF (HKUST-1) and subsequent carbonization that alters the surface composition, with improved activity and faradaic efficiency (FE) towards selective CO<small><sub>2</sub></small> reduction. The evaluation of electrocatalytic performance reveals that the synthesized catalyst exhibits enhanced electrocatalytic activity and selectivity with a FE<small><sub>CO</sub></small> of ∼ 90% at −0.79 V<small><sub>RHE</sub></small> and a current density (<em>j</em>) of 44.15 mA cm<small><sup>−2</sup></small> compared to Ag-NPs and Cu/C. The durability test over 40 h confirms the outstanding stability of Ag–Cu NPs/C. The lower Tafel slope value of only 75 mV dec<small><sup>−1</sup></small> corresponds to the fast reaction kinetics on the surface of Ag–Cu NPs/C. The synthetic protocol in this work offers an easy approach to the betterment of a cost-effective electrocatalyst with improved FE.</p>","PeriodicalId":72913,"journal":{"name":"Energy advances","volume":null,"pages":null},"PeriodicalIF":3.2000,"publicationDate":"2024-08-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2024/ya/d4ya00462k?page=search","citationCount":"0","resultStr":"{\"title\":\"Selective electroreduction of CO2 into CO over Ag and Cu decorated carbon nanoflakes†\",\"authors\":\"Ahmad Faraz, Waheed Iqbal, Shayan Gul, Fehmida K. Kanodarwala, Muhammad Nadeem Zafar, Guobao Xu and Muhammad Arif Nadeem\",\"doi\":\"10.1039/D4YA00462K\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >The electrocatalytic CO<small><sub>2</sub></small> reduction reaction (eCO<small><sub>2</sub></small>RR) has the potential to effectively cut carbon emission. However, the activity and selectivity of eCO<small><sub>2</sub></small>RR catalysts are topical due to the intricacy of the reaction components and mechanism. Herein, we have decorated silver and copper nanoparticles over carbon nanoflakes to achieve an Ag–Cu NPs/C system that enables selective reduction of CO<small><sub>2</sub></small> into CO. The catalyst is prepared by incorporating Ag nanoparticles into a Cu-BTC MOF (HKUST-1) and subsequent carbonization that alters the surface composition, with improved activity and faradaic efficiency (FE) towards selective CO<small><sub>2</sub></small> reduction. The evaluation of electrocatalytic performance reveals that the synthesized catalyst exhibits enhanced electrocatalytic activity and selectivity with a FE<small><sub>CO</sub></small> of ∼ 90% at −0.79 V<small><sub>RHE</sub></small> and a current density (<em>j</em>) of 44.15 mA cm<small><sup>−2</sup></small> compared to Ag-NPs and Cu/C. The durability test over 40 h confirms the outstanding stability of Ag–Cu NPs/C. The lower Tafel slope value of only 75 mV dec<small><sup>−1</sup></small> corresponds to the fast reaction kinetics on the surface of Ag–Cu NPs/C. The synthetic protocol in this work offers an easy approach to the betterment of a cost-effective electrocatalyst with improved FE.</p>\",\"PeriodicalId\":72913,\"journal\":{\"name\":\"Energy advances\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":3.2000,\"publicationDate\":\"2024-08-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://pubs.rsc.org/en/content/articlepdf/2024/ya/d4ya00462k?page=search\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Energy advances\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2024/ya/d4ya00462k\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Energy advances","FirstCategoryId":"1085","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/ya/d4ya00462k","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

摘要

电催化二氧化碳还原反应(eCO2RR)具有有效减少碳排放的潜力。然而,由于反应组分和机理的复杂性,eCO2RR 催化剂的活性和选择性一直是个难题。在此,我们将银纳米颗粒和铜纳米颗粒装饰在纳米碳片上,得到了一种银-铜 NPs/C 系统,该系统可将 CO2 选择性地还原成 CO。该催化剂的制备方法是将银纳米颗粒加入铜-四氯化碳 MOF(HKUST-1),然后进行碳化,从而改变其表面成分,从而提高了选择性还原 CO2 的活性和法拉第效率(FE)。电催化性能评估结果表明,与 Ag-NPs 和 Cu/C 相比,合成催化剂的电催化活性和选择性均有所提高,在 -0.79 VRHE 条件下的 FECO 为 90%,电流密度 (j) 为 44.15 mA cm-2。超过 40 小时的耐久性测试证实了 Ag-Cu NPs/C 的出色稳定性。仅为 75 mV dec-1 的较低 Tafel 斜坡值与 Ag-Cu NPs/C 表面的快速反应动力学相吻合。这项工作中的合成方案提供了一种简便的方法,可以更好地改进具有成本效益的电催化剂,并提高其 FE。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Selective electroreduction of CO2 into CO over Ag and Cu decorated carbon nanoflakes†

The electrocatalytic CO2 reduction reaction (eCO2RR) has the potential to effectively cut carbon emission. However, the activity and selectivity of eCO2RR catalysts are topical due to the intricacy of the reaction components and mechanism. Herein, we have decorated silver and copper nanoparticles over carbon nanoflakes to achieve an Ag–Cu NPs/C system that enables selective reduction of CO2 into CO. The catalyst is prepared by incorporating Ag nanoparticles into a Cu-BTC MOF (HKUST-1) and subsequent carbonization that alters the surface composition, with improved activity and faradaic efficiency (FE) towards selective CO2 reduction. The evaluation of electrocatalytic performance reveals that the synthesized catalyst exhibits enhanced electrocatalytic activity and selectivity with a FECO of ∼ 90% at −0.79 VRHE and a current density (j) of 44.15 mA cm−2 compared to Ag-NPs and Cu/C. The durability test over 40 h confirms the outstanding stability of Ag–Cu NPs/C. The lower Tafel slope value of only 75 mV dec−1 corresponds to the fast reaction kinetics on the surface of Ag–Cu NPs/C. The synthetic protocol in this work offers an easy approach to the betterment of a cost-effective electrocatalyst with improved FE.

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
CiteScore
1.80
自引率
0.00%
发文量
0
期刊最新文献
Boosting Ethylene Yield via Synergistic 2D/0D Nanostructured VCu Layered Double Hydroxide/TiO2 Catalyst in Electrochemical CO2 Reduction Effective electrochemical water oxidation to H2O2 based on bimetallic Fe/Co metal-organic framework Open Circuit Voltage of an All-Vanadium Redox Flow Battery as a Function of the State of Charge obtained from UV-Vis Spectroscopy Back cover Ag-NiP Deposited Green Carbon Channels Embedded NiP Panels for Sustainable Water Splitting
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1