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Electrochemical promotion of Ru nanoparticles deposited on a proton conductor electrolyte during CO2 hydrogenation

机译:CO2氢化过程中沉积在质子导体电解质上的Ru纳米粒子的电化学促进

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摘要

Recycling CO2 into a carbon-neutral source is a beneficial approach in reducing non-renewable energy sources. Herein, the electrochemical promotion of catalysis (EPOC) has been exploited to enhance the catalytic activity of Ru nanoparticles (0.7-1 nm) deposited on the proton conductor yttria-doped barium zirconate (BZY), as freestanding nanoparticles and supported on Co3O4 semiconductor, for CO2 hydrogenation. Under 250-450 degrees C and atmospheric pressure, both methanation and reverse water-gas shift (RWGS) reaction take place simultaneously over the Ru nanoparticles with a superior selectivity to CO. Under anodic polarization, free-standing Ru nanoparticles displayed an increase in CH4 and a decrease in CO production, while the opposite effect was observed under cathodic polarization. Ru supported on Co3O4 displayed a superior catalytic activity mostly due to enhanced metal-support interactions. The electronic effects induced by the pairing of Co3O4 and BZY resulted in a new approach to EPOC applications that brings it closer to industrial application.
机译:将CO2回收到碳中性源是减少不可再生能源的有益方法。在此,已经利用催化催化的电化学促进(EPOC)以增强Ru纳米粒子(0.7-1nm)的催化活性沉积在质子导体yttrai掺杂钡锆锆酸钡(BZY)上,作为独立式纳米颗粒并负载在Co3O4半导体上,用于CO2氢化。低于250-450℃和大气压,甲烷化和逆向水 - 气体移位(RWGS)反应在Ru纳米粒子上同时进行,具有优异的合作选择性。在阳极偏振下,立式Ru纳米粒子显示CH4的增加和CO生产的降低,而在阴极极化下观察到相反的效果。 Co3O4支持的Ru主要由于增强的金属支持相互作用而显示出优异的催化活性。 CO3O4和BZY配对引起的电子效果导致了EPOC应用的新方法,使其更接近工业应用。

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