Unconventional grain fragmentation creates high-density boundaries for efficient CO2-to-C2+ electro-conversion at ampere-level current density

IF 16.8 1区 材料科学 Q1 CHEMISTRY, PHYSICAL
Junjie Ding , Qianling Song , Lu Xia , Lujie Ruan , Min Zhang , Chaogang Ban , Jiazhi Meng , Jiangping Ma , Yajie Feng , Yang Wang , Xiaoping Tao , Danmei Yu , Ji-Yan Dai , Liyong Gan , Xiaoyuan Zhou
{"title":"Unconventional grain fragmentation creates high-density boundaries for efficient CO2-to-C2+ electro-conversion at ampere-level current density","authors":"Junjie Ding ,&nbsp;Qianling Song ,&nbsp;Lu Xia ,&nbsp;Lujie Ruan ,&nbsp;Min Zhang ,&nbsp;Chaogang Ban ,&nbsp;Jiazhi Meng ,&nbsp;Jiangping Ma ,&nbsp;Yajie Feng ,&nbsp;Yang Wang ,&nbsp;Xiaoping Tao ,&nbsp;Danmei Yu ,&nbsp;Ji-Yan Dai ,&nbsp;Liyong Gan ,&nbsp;Xiaoyuan Zhou","doi":"10.1016/j.nanoen.2024.109945","DOIUrl":null,"url":null,"abstract":"<div><p>Electrocatalytic CO<sub>2</sub> reduction reaction (CO<sub>2</sub>RR) to produce multi-carbon products (C<sub>2+</sub>) is one of the most sustainable manners to achieve net-zero carbon emissions. Among many approaches, enriching grain boundaries (GBs) in copper (Cu) catalysts has been demonstrated to enable enhancement for C<sub>2+</sub> production. However, it still lacks effective strategies to controllably synthesize abundant GBs, rendering efficient C<sub>2+</sub> production a persistent challenge, especially at ampere-level current density. Herein, we propose a novel strategy, which can achieve unconventional grain fragmentation during thermal annealing and thus create controllable GB densities. The catalyst with the utmost GB density exhibits a peak C<sub>2+</sub> faradaic efficiency of <em>ca.</em> 70.0 % in H-type cell and 68.2 % in flow cell; even more impressively, it delivers an ultra-high C<sub>2+</sub> current density of 0.768 A cm<sup>−2</sup>, outperforming most recently reported results. A combination of <em>in situ</em> spectroscopies and theoretical calculations reveal that the enrichment of GBs yields more active sites for a higher *CO coverage, leading to promotion of the *CO-*CO coupling process and ultimately high C<sub>2+</sub> production performance.</p></div>","PeriodicalId":394,"journal":{"name":"Nano Energy","volume":null,"pages":null},"PeriodicalIF":16.8000,"publicationDate":"2024-07-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nano Energy","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2211285524006943","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

Abstract

Electrocatalytic CO2 reduction reaction (CO2RR) to produce multi-carbon products (C2+) is one of the most sustainable manners to achieve net-zero carbon emissions. Among many approaches, enriching grain boundaries (GBs) in copper (Cu) catalysts has been demonstrated to enable enhancement for C2+ production. However, it still lacks effective strategies to controllably synthesize abundant GBs, rendering efficient C2+ production a persistent challenge, especially at ampere-level current density. Herein, we propose a novel strategy, which can achieve unconventional grain fragmentation during thermal annealing and thus create controllable GB densities. The catalyst with the utmost GB density exhibits a peak C2+ faradaic efficiency of ca. 70.0 % in H-type cell and 68.2 % in flow cell; even more impressively, it delivers an ultra-high C2+ current density of 0.768 A cm−2, outperforming most recently reported results. A combination of in situ spectroscopies and theoretical calculations reveal that the enrichment of GBs yields more active sites for a higher *CO coverage, leading to promotion of the *CO-*CO coupling process and ultimately high C2+ production performance.

Abstract Image

非常规晶粒破碎为安培级电流密度下二氧化碳到二氧化碳+的高效电转化创造了高密度边界
通过电催化二氧化碳还原反应(CO2RR)生产多碳产品(C2+)是实现净零碳排放的最可持续方法之一。在众多方法中,在铜(Cu)催化剂中富集晶界(GBs)已被证明能够提高 C2+ 的生产。然而,目前仍缺乏有效的策略来可控地合成丰富的 GBs,从而使 C2+ 的高效生产成为一项长期挑战,尤其是在安培级电流密度下。在此,我们提出了一种新颖的策略,它能在热退火过程中实现非常规的晶粒破碎,从而产生可控的 GB 密度。具有最高 GB 密度的催化剂在 H 型电池中显示出约 70.0% 的峰值 C2+ 法拉第效率,在流动电池中显示出 68.2% 的峰值 C2+ 法拉第效率;更令人印象深刻的是,它能提供 0.768 A cm-2 的超高 C2+ 电流密度,超过了最近报道的大多数结果。结合原位光谱和理论计算发现,GBs 的富集产生了更多的活性位点,以获得更高的*CO 覆盖率,从而促进了*CO-*CO 耦合过程,最终实现了高 C2+ 生成性能。
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
Nano Energy
Nano Energy CHEMISTRY, PHYSICAL-NANOSCIENCE & NANOTECHNOLOGY
CiteScore
30.30
自引率
7.40%
发文量
1207
审稿时长
23 days
期刊介绍: Nano Energy is a multidisciplinary, rapid-publication forum of original peer-reviewed contributions on the science and engineering of nanomaterials and nanodevices used in all forms of energy harvesting, conversion, storage, utilization and policy. Through its mixture of articles, reviews, communications, research news, and information on key developments, Nano Energy provides a comprehensive coverage of this exciting and dynamic field which joins nanoscience and nanotechnology with energy science. The journal is relevant to all those who are interested in nanomaterials solutions to the energy problem. Nano Energy publishes original experimental and theoretical research on all aspects of energy-related research which utilizes nanomaterials and nanotechnology. Manuscripts of four types are considered: review articles which inform readers of the latest research and advances in energy science; rapid communications which feature exciting research breakthroughs in the field; full-length articles which report comprehensive research developments; and news and opinions which comment on topical issues or express views on the developments in related fields.
×
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