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在电催化尿素合成的C-N偶联中,电子缺乏比电导率更重要。

Electron Deficiency is More Important than Conductivity in C-N Coupling for Electrocatalytic Urea Synthesis.

作者信息

Wang Yujie, Zhu Xiaorong, An Qizheng, Zhang Xiaoran, Wei Xiaoxiao, Chen Chen, Li Han, Chen Dawei, Zhou Yangyang, Liu Qinghua, Shao Huaiyu, Wang Shuangyin

机构信息

State Key Laboratory of Chem/Bio-Sensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University Changsha, Hunan, 410082, P. R. China.

School of Chemistry and Chemical Engineering, Nantong University Nantong, Jiangsu, 226019, P. R. China.

出版信息

Angew Chem Int Ed Engl. 2024 Dec 2;63(49):e202410938. doi: 10.1002/anie.202410938. Epub 2024 Nov 2.

Abstract

The electrocatalytic C-N coupling from CO and nitrate emerges as one of the solutions for waste upgrading and urea synthesis. In this work, we constructed electron-deficient Cu sites by the strong metal-polymer semiconductor interaction, to boost efficient and durable urea synthesis. In situ Raman spectroscopy identified the existence of electron-deficient Cu sites and was able to withstand electrochemical reduction conditions. Operando synchrotron-radiation Fourier transform infrared spectroscopy and theoretical calculations disclosed the vital role of electron-deficient Cu in adsorption and C-N coupling of oxygen-containing species. The electron-deficient Cu displayed a high urea yield rate of 255.0 mmol h g at -1.4 V versus the reversible hydrogen electrode and excellent electrochemical durability, superior than that of non-electron-deficient counterpart with conductive carbon material as the support. It can be concluded that the regulation of site electronic structure is more important than the optimization of catalyst conductive properties in the C-N coupling reactions.

摘要

由一氧化碳和硝酸盐进行的电催化碳氮偶联反应成为废物升级和尿素合成的解决方案之一。在这项工作中,我们通过强金属-聚合物-半导体相互作用构建了缺电子铜位点,以促进高效且持久的尿素合成。原位拉曼光谱确定了缺电子铜位点的存在,并且能够承受电化学还原条件。操作同步辐射傅里叶变换红外光谱和理论计算揭示了缺电子铜在含氧物种的吸附和碳氮偶联中的关键作用。缺电子铜在相对于可逆氢电极-1.4 V的电位下显示出255.0 mmol h g的高尿素产率以及优异的电化学耐久性,优于以导电碳材料为载体的非缺电子对应物。可以得出结论,在碳氮偶联反应中,位点电子结构的调控比催化剂导电性能的优化更为重要。

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