Engineering the electron localization of metal sites on nanosheets assembled periodic macropores for CO2 photoreduction

IF 15.7 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES Nature Communications Pub Date : 2024-12-04 DOI:10.1038/s41467-024-54988-3
Wenyuan Lyu, Yang Liu, Datong Chen, Fengliang Wang, Yingwei Li
{"title":"Engineering the electron localization of metal sites on nanosheets assembled periodic macropores for CO2 photoreduction","authors":"Wenyuan Lyu, Yang Liu, Datong Chen, Fengliang Wang, Yingwei Li","doi":"10.1038/s41467-024-54988-3","DOIUrl":null,"url":null,"abstract":"<p>Photocatalytic conversion of CO<sub>2</sub> into syngas is highly appealing, yet still suffers from the undesirable product yield due to the sluggish carrier transfer and the uncontrollable affinity between catalytic sites and intermediates. Here we report the fabrication of Co sites with tunable electron localization capability on two dimensional (2D) nanosheets assembled three dimensional (3D) ordered macroporous framework (3DOM-NS). The as-prepared Co-based 3DOM-NS catalysts exhibit attractive photocatalytic performances toward CO<sub>2</sub> reduction, among which the cobalt sulfide one (3DOM Co-SNS) shows the highest syngas generation rate up to 347.3 μmol h<sup>−1</sup> under the irradiation of visible light and delivers a remarkable catalytic activity (1150.7 μmol h<sup>−1</sup>) in a flow reaction system under natural sunlight. Mechanism studies reveal that the high electron localization of metal sites in 3DOM Co-SNS strengthens the interaction between Co and HCOO* via the orbital interactions of <i>d</i><sub><i>yz</i></sub>/<i>d</i><sub><i>xz</i></sub>-<i>p</i> and <i>s</i>-<i>s</i>, thus facilitating the cleaving process of C-O bond. Additionally, the ordered macroporous framework with nanosheet subunits elevates the transfer efficiency of photoexcited electrons, which contributes to its high activity.</p>","PeriodicalId":19066,"journal":{"name":"Nature Communications","volume":"1 1","pages":""},"PeriodicalIF":15.7000,"publicationDate":"2024-12-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature Communications","FirstCategoryId":"103","ListUrlMain":"https://doi.org/10.1038/s41467-024-54988-3","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Photocatalytic conversion of CO2 into syngas is highly appealing, yet still suffers from the undesirable product yield due to the sluggish carrier transfer and the uncontrollable affinity between catalytic sites and intermediates. Here we report the fabrication of Co sites with tunable electron localization capability on two dimensional (2D) nanosheets assembled three dimensional (3D) ordered macroporous framework (3DOM-NS). The as-prepared Co-based 3DOM-NS catalysts exhibit attractive photocatalytic performances toward CO2 reduction, among which the cobalt sulfide one (3DOM Co-SNS) shows the highest syngas generation rate up to 347.3 μmol h−1 under the irradiation of visible light and delivers a remarkable catalytic activity (1150.7 μmol h−1) in a flow reaction system under natural sunlight. Mechanism studies reveal that the high electron localization of metal sites in 3DOM Co-SNS strengthens the interaction between Co and HCOO* via the orbital interactions of dyz/dxz-p and s-s, thus facilitating the cleaving process of C-O bond. Additionally, the ordered macroporous framework with nanosheet subunits elevates the transfer efficiency of photoexcited electrons, which contributes to its high activity.

Abstract Image

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
设计纳米片上金属位的电子定位,组装周期大孔,用于CO2光还原
光催化将CO2转化为合成气是非常有吸引力的,但由于载体转移缓慢和催化位点与中间体之间的亲和力不可控,仍然存在不良的产物收率。本文报道了在三维有序大孔框架(3DOM-NS)组装的二维(2D)纳米片上制备具有可调电子定位能力的钴位点。所制备的钴基3DOM- sns催化剂对CO2还原具有良好的光催化性能,其中硫化钴(3DOM - sns)在可见光照射下合成气生成率最高,达到347.3 μmol h−1,在自然光照下流动反应体系中催化活性达到1150.7 μmol h−1。机理研究表明,3DOM Co- sns中金属位的高电子局域化通过dyz/dxz-p和s-s轨道相互作用加强了Co与HCOO*之间的相互作用,从而促进了C-O键的断裂过程。此外,具有纳米片亚基的有序大孔框架提高了光激发电子的转移效率,这有助于其高活性。
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 去求助
文献相关原料
公司名称
产品信息
麦克林
Triethanolamine
麦克林
Triethanolamine
麦克林
Triethanolamine
麦克林
Triethanolamine
阿拉丁
Furfuryl alcohol
阿拉丁
5-Hydroxymethyl-2-furaldehyde
阿拉丁
Benzyl alcohol
阿拉丁
Tris(2,2′-bipyridine) dichlororuthenium(II) hexahydrate
阿拉丁
Zinc nitrate hexahydrate
阿拉丁
Copper nitrate trihydrate
阿拉丁
Iron nitrate nonahydrate
阿拉丁
Nickel nitrate hexahydrate
阿拉丁
Selenium
阿拉丁
Sodium hypophosphite monohydrate
阿拉丁
Thioacetamide
阿拉丁
Cobalt acetate tetrahydrate
阿拉丁
2-methylimidazole
阿拉丁
Potassium persulfate
阿拉丁
Styrene
阿拉丁
Ammonium hydroxide
阿拉丁
Cobalt nitrate hexahydrate
阿拉丁
Thioacetamide
阿拉丁
Cobalt acetate tetrahydrate
阿拉丁
2-Methylimidazole
阿拉丁
Potassium persulfate
阿拉丁
Styrene
阿拉丁
Ammonium hydroxide
阿拉丁
Cobalt nitrate hexahydrate
阿拉丁
Furfuryl alcohol
阿拉丁
5-Hydroxymethyl-2-furaldehyde
阿拉丁
Benzyl alcohol
阿拉丁
Tris(2,2′-bipyridine) dichlororuthenium(II) hexahydrate
阿拉丁
Zinc nitrate hexahydrate
阿拉丁
Copper nitrate trihydrate
阿拉丁
Iron nitrate nonahydrate
阿拉丁
Nickel nitrate hexahydrate
阿拉丁
Selenium
阿拉丁
Sodium hypophosphite monohydrate
阿拉丁
Thioacetamide
阿拉丁
Cobalt acetate tetrahydrate
阿拉丁
2-Methylimidazole
阿拉丁
Potassium persulfate
阿拉丁
Styrene
阿拉丁
Ammonium hydroxide
阿拉丁
Cobalt nitrate hexahydrate
阿拉丁
2-Methylimidazole
阿拉丁
Potassium persulfate
阿拉丁
Styrene
阿拉丁
Ammonium hydroxide
阿拉丁
Cobalt nitrate hexahydrate
阿拉丁
Furfuryl alcohol
阿拉丁
5-Hydroxymethyl-2-furaldehyde
阿拉丁
Benzyl alcohol
阿拉丁
Tris(2,2′-bipyridine) dichlororuthenium(II) hexahydrate
阿拉丁
Zinc nitrate hexahydrate
阿拉丁
Copper nitrate trihydrate
阿拉丁
Iron nitrate nonahydrate
阿拉丁
Nickel nitrate hexahydrate
阿拉丁
Selenium
阿拉丁
Sodium hypophosphite monohydrate
阿拉丁
Thioacetamide
阿拉丁
Cobalt acetate tetrahydrate
阿拉丁
Furfuryl alcohol
阿拉丁
5-Hydroxymethyl-2-furaldehyde
阿拉丁
Benzyl alcohol
阿拉丁
Tris(2,2′-bipyridine) dichlororuthenium(II) hexahydrate
阿拉丁
Zinc nitrate hexahydrate
阿拉丁
Copper nitrate trihydrate
阿拉丁
Iron nitrate nonahydrate
阿拉丁
Nickel nitrate hexahydrate
阿拉丁
Selenium
阿拉丁
Sodium hypophosphite monohydrate
来源期刊
Nature Communications
Nature Communications Biological Science Disciplines-
CiteScore
24.90
自引率
2.40%
发文量
6928
审稿时长
3.7 months
期刊介绍: Nature Communications, an open-access journal, publishes high-quality research spanning all areas of the natural sciences. Papers featured in the journal showcase significant advances relevant to specialists in each respective field. With a 2-year impact factor of 16.6 (2022) and a median time of 8 days from submission to the first editorial decision, Nature Communications is committed to rapid dissemination of research findings. As a multidisciplinary journal, it welcomes contributions from biological, health, physical, chemical, Earth, social, mathematical, applied, and engineering sciences, aiming to highlight important breakthroughs within each domain.
期刊最新文献
Dissecting PGE2-driven inhibition of T cell activation using single-cell multi-omic and inflammatory bowel disease genetic association analysis. ASO therapy rescues NOTCH2NLC GGC repeat expansion-induced genomic damage, 3D chromatin structural abnormalities, and senescence. Scalable Ni‑driven synthesis of Pt single‑site catalysts for hydrogen evolution. Influence of B cell-lineage targeted CAR-T cell therapy on humoral immunity and vaccine-induced antibody response. Genomic analysis of high pathogenicity avian influenza viruses from Antarctica reveals multiple introductions from South America.
×
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:604180095
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