Yu Li
(, ), Haojun Shi
(, ), Congcong Li
(, ), Zhongliang Liu
(, ), Weizheng Tang
(, ), Tingting Zhang
(, ), Shixin Yin
(, ), Huihui Li
(, ), Chunzhong Li
(, )
{"title":"Shaping hollow spherical assemblies for enhanced Cu0/Cu+ interface to boost C2+ selectivity in CO2 electroreduction","authors":"Yu Li \n (, ), Haojun Shi \n (, ), Congcong Li \n (, ), Zhongliang Liu \n (, ), Weizheng Tang \n (, ), Tingting Zhang \n (, ), Shixin Yin \n (, ), Huihui Li \n (, ), Chunzhong Li \n (, )","doi":"10.1007/s40843-024-3057-1","DOIUrl":null,"url":null,"abstract":"<div><p>The creation of Cu<sup>0</sup>/Cu<sup>+</sup> interface over Cu-based catalysts is known to facilitate the production of multi-carbon (C<sub>2+</sub>) products during CO<sub>2</sub> reduction reaction (CO<sub>2</sub> RR). However, the Cu<sup>+</sup> moieties exhibit high susceptibility towards reduction into Cu<sup>0</sup> at a high current density. Thus, a comprehensive understanding and rational shaping strategy for the construction and stabilization of Cu<sup>0</sup>/Cu<sup>+</sup> interface in Cu-based catalysts is imperative. Herein, we proposed a controllable “nanoparticle assembly” strategy to obtain hollow spherical assemblies (HSA) composed of numerous Cu<sub>2</sub>O nanoparticles (HSA-Cu<sub>2</sub>O). The HSA-Cu<sub>2</sub>O catalysts significantly enhance the selectivity of C<sub>2+</sub> products, resulting in an impressive overall Faraday efficiency (FE) of 79.2% ± 0.7% at a partial current density of 317.1 mA cm<sup>−2</sup>. The HSA-Cu<sub>2</sub>O catalysts undergo <i>in-situ</i> electrochemically reconstruction during CO<sub>2</sub>RR, achieving Cu<sup>0</sup>/Cu<sup>+</sup> interfacial sites with a high density. The Auger electron spectra, <i>in-situ</i> Raman, and morphological evolution studies have confirmed that the combination of the Cu<sup>0</sup>/Cu<sup>+</sup> interface and hollow sphere architecture facilitated the concentration of *CO intermediates, thereby promoting C–C dimerization to boost C<sub>2+</sub> selectivity in CO<sub>2</sub>RR.</p><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":773,"journal":{"name":"Science China Materials","volume":"67 11","pages":"3596 - 3601"},"PeriodicalIF":6.8000,"publicationDate":"2024-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Science China Materials","FirstCategoryId":"88","ListUrlMain":"https://link.springer.com/article/10.1007/s40843-024-3057-1","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
The creation of Cu0/Cu+ interface over Cu-based catalysts is known to facilitate the production of multi-carbon (C2+) products during CO2 reduction reaction (CO2 RR). However, the Cu+ moieties exhibit high susceptibility towards reduction into Cu0 at a high current density. Thus, a comprehensive understanding and rational shaping strategy for the construction and stabilization of Cu0/Cu+ interface in Cu-based catalysts is imperative. Herein, we proposed a controllable “nanoparticle assembly” strategy to obtain hollow spherical assemblies (HSA) composed of numerous Cu2O nanoparticles (HSA-Cu2O). The HSA-Cu2O catalysts significantly enhance the selectivity of C2+ products, resulting in an impressive overall Faraday efficiency (FE) of 79.2% ± 0.7% at a partial current density of 317.1 mA cm−2. The HSA-Cu2O catalysts undergo in-situ electrochemically reconstruction during CO2RR, achieving Cu0/Cu+ interfacial sites with a high density. The Auger electron spectra, in-situ Raman, and morphological evolution studies have confirmed that the combination of the Cu0/Cu+ interface and hollow sphere architecture facilitated the concentration of *CO intermediates, thereby promoting C–C dimerization to boost C2+ selectivity in CO2RR.
期刊介绍:
Science China Materials (SCM) is a globally peer-reviewed journal that covers all facets of materials science. It is supervised by the Chinese Academy of Sciences and co-sponsored by the Chinese Academy of Sciences and the National Natural Science Foundation of China. The journal is jointly published monthly in both printed and electronic forms by Science China Press and Springer. The aim of SCM is to encourage communication of high-quality, innovative research results at the cutting-edge interface of materials science with chemistry, physics, biology, and engineering. It focuses on breakthroughs from around the world and aims to become a world-leading academic journal for materials science.