胺官能化表面受挫路易斯对促进二氧化碳光催化

EES catalysis Pub Date : 2024-01-09 DOI:10.1039/D3EY00261F
Qinhui Guan, Chengzhe Ni, Tingjiang Yan, Na Li, Lu Wang, Zhe Lu, Weiguang Ran, Yipin Zhang, Wenjuan Li, Lulu Zhang, Dapeng Zhang, Baibiao Huang and Geoffrey A. Ozin
{"title":"胺官能化表面受挫路易斯对促进二氧化碳光催化","authors":"Qinhui Guan, Chengzhe Ni, Tingjiang Yan, Na Li, Lu Wang, Zhe Lu, Weiguang Ran, Yipin Zhang, Wenjuan Li, Lulu Zhang, Dapeng Zhang, Baibiao Huang and Geoffrey A. Ozin","doi":"10.1039/D3EY00261F","DOIUrl":null,"url":null,"abstract":"<p >The archetype surface frustrated Lewis pair (SFLP) that facilitates CO<small><sub>2</sub></small> photocatalytic hydrogenation to methanol and carbon monoxide, is an InOH⋯In site positioned in the surface of a nanoscale indium oxide hydroxide, denoted In<small><sub>2</sub></small>O<small><sub>3−<em>x</em></sub></small>(OH)<small><sub><em>y</em></sub></small>. Proximal Lewis acid In(<small>III</small>) and Lewis base InOH of this genre serve as surface active sites that enable the photochemical heterolytic H<small><sub>2</sub></small> dissociation and reduction of CO<small><sub>2</sub></small> to the mentioned products. The conversion rate enabled by light has been found to far exceed that enabled by heat. Efforts to enhance the CO<small><sub>2</sub></small> photocatalytic performance of the SFLP have involved modifications of the Lewis acidity and basicity through isomorphic substitution of In(<small>III</small>) with Bi(<small>III</small>) and changes in the population of oxygen vacancies through control of oxide non-stoichiometry. Replacement of the Lewis base hydroxide InOH by the stronger Lewis base amine InNH<small><sub>2</sub></small> heretofore remains unexplored. The strategy described herein to explore this opportunity begins with the synthesis of In<small><sub>2</sub></small>O<small><sub>3−<em>x</em></sub></small>(EDA)<small><sub><em>y</em></sub></small>. This new material is proven to contain an InNH<small><sub>2</sub></small>⋯In SFLP and its CO<small><sub>2</sub></small> photocatalytic performance is demonstrated to outperform that of its In<small><sub>2</sub></small>O<small><sub>3−<em>x</em></sub></small>(OH)<small><sub><em>y</em></sub></small> progenitor. Tailored Lewis acidity and basicity surfaces bring CO<small><sub>2</sub></small> photocatalysis another step closer to the vision of solar CO<small><sub>2</sub></small> refineries.</p>","PeriodicalId":72877,"journal":{"name":"EES catalysis","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-01-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2024/ey/d3ey00261f?page=search","citationCount":"0","resultStr":"{\"title\":\"Amine functionalized surface frustrated Lewis pairs boost CO2 photocatalysis†‡\",\"authors\":\"Qinhui Guan, Chengzhe Ni, Tingjiang Yan, Na Li, Lu Wang, Zhe Lu, Weiguang Ran, Yipin Zhang, Wenjuan Li, Lulu Zhang, Dapeng Zhang, Baibiao Huang and Geoffrey A. Ozin\",\"doi\":\"10.1039/D3EY00261F\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >The archetype surface frustrated Lewis pair (SFLP) that facilitates CO<small><sub>2</sub></small> photocatalytic hydrogenation to methanol and carbon monoxide, is an InOH⋯In site positioned in the surface of a nanoscale indium oxide hydroxide, denoted In<small><sub>2</sub></small>O<small><sub>3−<em>x</em></sub></small>(OH)<small><sub><em>y</em></sub></small>. Proximal Lewis acid In(<small>III</small>) and Lewis base InOH of this genre serve as surface active sites that enable the photochemical heterolytic H<small><sub>2</sub></small> dissociation and reduction of CO<small><sub>2</sub></small> to the mentioned products. The conversion rate enabled by light has been found to far exceed that enabled by heat. Efforts to enhance the CO<small><sub>2</sub></small> photocatalytic performance of the SFLP have involved modifications of the Lewis acidity and basicity through isomorphic substitution of In(<small>III</small>) with Bi(<small>III</small>) and changes in the population of oxygen vacancies through control of oxide non-stoichiometry. Replacement of the Lewis base hydroxide InOH by the stronger Lewis base amine InNH<small><sub>2</sub></small> heretofore remains unexplored. The strategy described herein to explore this opportunity begins with the synthesis of In<small><sub>2</sub></small>O<small><sub>3−<em>x</em></sub></small>(EDA)<small><sub><em>y</em></sub></small>. This new material is proven to contain an InNH<small><sub>2</sub></small>⋯In SFLP and its CO<small><sub>2</sub></small> photocatalytic performance is demonstrated to outperform that of its In<small><sub>2</sub></small>O<small><sub>3−<em>x</em></sub></small>(OH)<small><sub><em>y</em></sub></small> progenitor. Tailored Lewis acidity and basicity surfaces bring CO<small><sub>2</sub></small> photocatalysis another step closer to the vision of solar CO<small><sub>2</sub></small> refineries.</p>\",\"PeriodicalId\":72877,\"journal\":{\"name\":\"EES catalysis\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-01-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://pubs.rsc.org/en/content/articlepdf/2024/ey/d3ey00261f?page=search\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"EES catalysis\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2024/ey/d3ey00261f\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"EES catalysis","FirstCategoryId":"1085","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/ey/d3ey00261f","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

促进二氧化碳光催化加氢生成甲醇和一氧化碳的典型表面挫折路易斯对(SFLP)是位于纳米级氢氧化铟(In2O3-x(OH)y)表面的InOH--In位点。这种类型的近端路易斯酸 In(III) 和路易斯碱 InOH 可作为表面活性位点,促成光化学异解 H2 和将 CO2 还原成上述产物。研究发现,光的转化率远远超过热的转化率。为了提高 SFLP 的 CO2 光催化性能,需要通过用 Bi(III)同构取代 In(III)来改变路易斯酸度和碱性,并通过控制氧化物的非全度来改变氧空位的数量。用更强的路易斯碱胺 InNH2 取代路易斯碱氢氧化物 InOH 的研究至今仍未进行。本文所述的探索这一机遇的策略始于 In2O3-x(EDA)y 的合成。事实证明,这种新材料含有 InNH2-In SFLP,其二氧化碳光催化性能优于其 In2O3-x(OH)y 原合物。量身定制的路易斯酸性和碱性表面使二氧化碳光催化离太阳能二氧化碳精炼厂的愿景又近了一步。
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

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
Amine functionalized surface frustrated Lewis pairs boost CO2 photocatalysis†‡

The archetype surface frustrated Lewis pair (SFLP) that facilitates CO2 photocatalytic hydrogenation to methanol and carbon monoxide, is an InOH⋯In site positioned in the surface of a nanoscale indium oxide hydroxide, denoted In2O3−x(OH)y. Proximal Lewis acid In(III) and Lewis base InOH of this genre serve as surface active sites that enable the photochemical heterolytic H2 dissociation and reduction of CO2 to the mentioned products. The conversion rate enabled by light has been found to far exceed that enabled by heat. Efforts to enhance the CO2 photocatalytic performance of the SFLP have involved modifications of the Lewis acidity and basicity through isomorphic substitution of In(III) with Bi(III) and changes in the population of oxygen vacancies through control of oxide non-stoichiometry. Replacement of the Lewis base hydroxide InOH by the stronger Lewis base amine InNH2 heretofore remains unexplored. The strategy described herein to explore this opportunity begins with the synthesis of In2O3−x(EDA)y. This new material is proven to contain an InNH2⋯In SFLP and its CO2 photocatalytic performance is demonstrated to outperform that of its In2O3−x(OH)y progenitor. Tailored Lewis acidity and basicity surfaces bring CO2 photocatalysis another step closer to the vision of solar CO2 refineries.

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
自引率
0.00%
发文量
0
期刊最新文献
Back cover Correction: High photocatalytic yield in the non-oxidative coupling of methane using a Pd–TiO2 nanomembrane gas flow-through reactor Embedding the intermetallic Pt5Ce alloy in mesopores through Pt–C coordination layer interactions as a stable electrocatalyst for the oxygen reduction reaction† Efficient CO2-to-CO conversion in dye-sensitized photocatalytic systems enabled by electrostatically-driven catalyst binding† Green energy driven methane conversion under mild conditions
×
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