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原子分散的铁/金界面上用于选择性CO电还原的协同调制

Synergistic Modulation at Atomically Dispersed Fe/Au Interface for Selective CO Electroreduction.

作者信息

Shen Xinyi, Liu Xiaokang, Wang Sicong, Chen Tao, Zhang Wei, Cao Linlin, Ding Tao, Lin Yue, Liu Dong, Wang Lan, Zhang Wei, Yao Tao

机构信息

National Synchrotron Radiation Laboratory, University of Science and Technology of China, Hefei 230029, P. R. China.

School of National Defense Science and Technology, Southwest University of Science and Technology, Mianyang 621010, P. R. China.

出版信息

Nano Lett. 2021 Jan 13;21(1):686-692. doi: 10.1021/acs.nanolett.0c04291. Epub 2020 Dec 11.

Abstract

The electrocatalytic carbon dioxide reduction reaction (CORR) offers an attractive route to fuels and feedstocks from renewable energy. Gold is active for the electrochemical CORR to CO, while the competing hydrogen evolution reaction is unavoidable. Here, we report a synergistic strategy, via introducing atomically dispersed Fe to tune the electronic structure of the Au nanoparticle, to improve the CO selectivity. By using operando X-ray absorption and infrared spectroscopies, we reveal the dynamic structural evolution and the adsorption of reactant intermediates at the single-atom Fe/Au interface. During the reaction, the interaction between Fe and Au atoms becomes stronger, and the Fe/Au synergies affect the adsorption of reaction intermediates, thus improving the selectivity of CO up to 96.3% with a mass activity of 399 mA mg. These results highlight the significant importance of synergistic modulation for advancing the single-atom decorated nanoparticle catalysis.

摘要

电催化二氧化碳还原反应(CORR)为利用可再生能源制取燃料和原料提供了一条颇具吸引力的途径。金对电化学CORR生成CO具有活性,而不可避免地会发生竞争性析氢反应。在此,我们报道了一种协同策略,即通过引入原子分散的铁来调节金纳米颗粒的电子结构,以提高CO选择性。通过使用原位X射线吸收和红外光谱,我们揭示了单原子铁/金界面处的动态结构演变和反应物中间体的吸附情况。在反应过程中,铁和金原子之间的相互作用增强,铁/金协同效应影响反应中间体的吸附,从而将CO选择性提高到96.3%,质量活性为399 mA mg。这些结果突出了协同调制对于推进单原子修饰纳米颗粒催化的重要意义。

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