Dual-site adsorption regulation on a bcc/fcc heterophase PdCuIn metallene for efficient urea electrosynthesis
You Xu1, Jiwei Zhang1, Youwei Sheng1
1State Key Laboratory of Green Chemical Synthesis and Conversion, Zhejiang Key Laboratory of Surface and Interface Science and Engineering for Catalysts, College of Chemical Engineering, Zhejiang University of Technology, Hangzhou 310014, P. R. China. yxu@zjut.edu.cn.
Abstract:
Electrochemical co-reduction of CO2 and nitrate to produce urea is a sustainable alternative to the Bosch-Meiser process, yet its practical application is impeded by slow C-N coupling kinetics and limited urea selectivity. Here, we design a bcc/fcc hetero-phase PdCuIn metallene (b/f-PdCuIn-ene) catalyst for urea electrosynthesis from CO2 and nitrate. The resultant b/f-PdCuIn-ene catalyst achieves a urea yield rate of 2096.2 μg h-1 mgcat.-1 and a faradaic efficiency of 37.7% at a low potential of -0.3 V vs. the reversible hydrogen electrode, along with good stability. Attenuated total reflection Fourier transform infrared spectroscopy verifies the generation of key *CO and *NH2 intermediates during the CO2/nitrate co-reduction process. Density functional theory calculations reveal that the bcc/fcc hetero-phase structure could balance the adsorption of *CO and *NH2 intermediates and promote the C-N coupling reaction for urea synthesis. This study provides an effective crystal phase engineering strategy for tailoring metallene catalysts toward urea electrosynthesis.
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