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Uncovering Atomic-Scale Stability and Reactivity in Engineered Zinc Oxide Electrocatalysts for Controllable Syngas Production

机译:揭示用于可控合成气生产的工程化氧化锌电催化剂的原子尺度稳定性和反应性

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Abstract In this study, scalable, flame spray synthesis is utilized to develop defective ZnO nanomaterials for the concurrent generation of H2 and CO during electrochemical CO2 reduction reactions (CO2RR). The designed ZnO achieves an H2/CO ratio of ≈1 with a large current density (j) of 40 mA cm−2 during long‐term continuous reaction at a cell voltage of 2.6 V. Through in situ atomic pair distribution function analysis, the remarkable stability of these ZnO structures is explored, addressing the knowledge gap in understanding the dynamics of oxide catalysts during CO2RR. Through optimization of synthesis conditions, ZnO facets are modulated which are shown to affect reaction selectivity, in agreement with theoretical calculations. These findings and insights on synthetic manipulation of active sites in defective metal‐oxides can be used as guidelines to develop active catalysts for syngas production for renewable power‐to‐X to generate a range of fuels and chemicals.
机译:摘要在本研究中,利用可伸缩的火焰喷雾合成来开发用于在电化学CO2还原反应(CO2RR)期间H2和CO的同时产生的缺陷ZnO纳米材料。设计的ZnO在长期连续反应下实现了40 mA cm-2的大电流密度(j)的H2 / Co比,在2.6V的电池电压下。通过原位原子对分布函数分析,所述探讨了这些ZnO结构的显着稳定性,解决了在CO 2R期间理解氧化物催化剂的动态的知识间隙。通过合成条件的优化,调节ZnO刻面,其显示出影响反应选择性,同时与理论计算。这些发现和关于有缺陷金属氧化物中活性位点的合成操纵的发现和见解可用作为可再生能源-TO-X产生合成气生产的活性催化剂,以产生一系列燃料和化学品。

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