{"title":"硒酸蚀刻辅助原子工程设计用于增强二氧化碳电还原的金属-半金属双单原子催化剂。","authors":"Minghong Huang, Sheng-Hua Zhou, Cheng-Jie Yang, Chung-Li Dong, Yingchun He, Wenbo Wei, Xiaofang Li, Qi-Long Zhu, Zhenguo Huang","doi":"10.1021/acsnano.4c12576","DOIUrl":null,"url":null,"abstract":"<p><p>Single-atom catalysts are promising for electrocatalytic CO<sub>2</sub> conversion but face challenges in controllable syntheses. Herein, a facile selenic acid etching-assisted strategy has been developed to fabricate a hybrid metal-semimetal dual single-atom catalyst for electrocatalytic CO<sub>2</sub> reduction. This strategy enables the simultaneous generation of monodisperse active sites and hierarchical morphologies with hollow nanostructures. The as-obtained catalyst with Fe-Se dual single-atom sites supported by porous nitrogen-doped carbon (FeSe-NC) shows exceptional catalytic activity and CO selectivity, delivering a Faradaic efficiency (FE) of >97% with industrially comparable <i>j</i><sub>CO</sub>, superior to the Fe single-atom catalyst. Moreover, the FeSe-NC-based rechargeable Zn-CO<sub>2</sub> battery delivers a high power density (2.01 mW cm<sup>-2</sup>) and outstanding FE<sub>CO</sub> (>90%), as well as excellent cycling stability. Experimental results together with theoretical calculations reveal that the etching-induced defects and the Se-modulated Fe centers with asymmetrical polarized charge distributions synergistically facilitate the key intermediate *CO desorption and thus accelerate the CO<sub>2</sub>-to-CO conversion.</p>","PeriodicalId":21,"journal":{"name":"ACS Nano","volume":" ","pages":"33210-33219"},"PeriodicalIF":16.0000,"publicationDate":"2024-12-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Selenic Acid Etching Assisted Atomic Engineering for Designing Metal-Semimetal Dual Single-Atom Catalysts for Enhanced CO<sub>2</sub> Electroreduction.\",\"authors\":\"Minghong Huang, Sheng-Hua Zhou, Cheng-Jie Yang, Chung-Li Dong, Yingchun He, Wenbo Wei, Xiaofang Li, Qi-Long Zhu, Zhenguo Huang\",\"doi\":\"10.1021/acsnano.4c12576\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Single-atom catalysts are promising for electrocatalytic CO<sub>2</sub> conversion but face challenges in controllable syntheses. Herein, a facile selenic acid etching-assisted strategy has been developed to fabricate a hybrid metal-semimetal dual single-atom catalyst for electrocatalytic CO<sub>2</sub> reduction. This strategy enables the simultaneous generation of monodisperse active sites and hierarchical morphologies with hollow nanostructures. The as-obtained catalyst with Fe-Se dual single-atom sites supported by porous nitrogen-doped carbon (FeSe-NC) shows exceptional catalytic activity and CO selectivity, delivering a Faradaic efficiency (FE) of >97% with industrially comparable <i>j</i><sub>CO</sub>, superior to the Fe single-atom catalyst. Moreover, the FeSe-NC-based rechargeable Zn-CO<sub>2</sub> battery delivers a high power density (2.01 mW cm<sup>-2</sup>) and outstanding FE<sub>CO</sub> (>90%), as well as excellent cycling stability. Experimental results together with theoretical calculations reveal that the etching-induced defects and the Se-modulated Fe centers with asymmetrical polarized charge distributions synergistically facilitate the key intermediate *CO desorption and thus accelerate the CO<sub>2</sub>-to-CO conversion.</p>\",\"PeriodicalId\":21,\"journal\":{\"name\":\"ACS Nano\",\"volume\":\" \",\"pages\":\"33210-33219\"},\"PeriodicalIF\":16.0000,\"publicationDate\":\"2024-12-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Nano\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://doi.org/10.1021/acsnano.4c12576\",\"RegionNum\":1,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/11/1 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Nano","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1021/acsnano.4c12576","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/11/1 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
摘要
单原子催化剂在电催化二氧化碳转化方面前景广阔,但在可控合成方面面临挑战。在此,我们开发了一种简便的硒酸蚀刻辅助策略,用于制造电催化二氧化碳还原的混合金属-半金属双单原子催化剂。该策略可同时生成单分散活性位点和具有中空纳米结构的分层形貌。由多孔掺氮碳(FeSe-NC)支撑的具有 Fe-Se 双单原子位点的催化剂显示出卓越的催化活性和二氧化碳选择性,其法拉第效率(FE)大于 97%,jCO 具有工业可比性,优于铁单原子催化剂。此外,基于 FeSe-NC 的可充电 Zn-CO2 电池具有高功率密度(2.01 mW cm-2)和出色的 FECO(>90%),以及卓越的循环稳定性。实验结果和理论计算显示,蚀刻诱导的缺陷和具有不对称极化电荷分布的 Se 调制铁中心协同促进了关键的中间 *CO 解吸,从而加速了 CO2 到 CO 的转化。
Selenic Acid Etching Assisted Atomic Engineering for Designing Metal-Semimetal Dual Single-Atom Catalysts for Enhanced CO2 Electroreduction.
Single-atom catalysts are promising for electrocatalytic CO2 conversion but face challenges in controllable syntheses. Herein, a facile selenic acid etching-assisted strategy has been developed to fabricate a hybrid metal-semimetal dual single-atom catalyst for electrocatalytic CO2 reduction. This strategy enables the simultaneous generation of monodisperse active sites and hierarchical morphologies with hollow nanostructures. The as-obtained catalyst with Fe-Se dual single-atom sites supported by porous nitrogen-doped carbon (FeSe-NC) shows exceptional catalytic activity and CO selectivity, delivering a Faradaic efficiency (FE) of >97% with industrially comparable jCO, superior to the Fe single-atom catalyst. Moreover, the FeSe-NC-based rechargeable Zn-CO2 battery delivers a high power density (2.01 mW cm-2) and outstanding FECO (>90%), as well as excellent cycling stability. Experimental results together with theoretical calculations reveal that the etching-induced defects and the Se-modulated Fe centers with asymmetrical polarized charge distributions synergistically facilitate the key intermediate *CO desorption and thus accelerate the CO2-to-CO conversion.
期刊介绍:
ACS Nano, published monthly, serves as an international forum for comprehensive articles on nanoscience and nanotechnology research at the intersections of chemistry, biology, materials science, physics, and engineering. The journal fosters communication among scientists in these communities, facilitating collaboration, new research opportunities, and advancements through discoveries. ACS Nano covers synthesis, assembly, characterization, theory, and simulation of nanostructures, nanobiotechnology, nanofabrication, methods and tools for nanoscience and nanotechnology, and self- and directed-assembly. Alongside original research articles, it offers thorough reviews, perspectives on cutting-edge research, and discussions envisioning the future of nanoscience and nanotechnology.