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Combined Simulation and Experimental Study of Electrolysis Flow Cell for Continuous CO_2 Conversion

机译:电解流动细胞连续CO_2转换的综合模拟与实验研究

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Electrochemical carbon dioxide reduction reaction (CO_2RR) is a promising strategy to sequester CO_2 while synthesizing valuable chemicals and utilizing intermittent renewable energy supply from solar and wind energy. Electrolysis is often studied in H-cells that are composed of planar electrodes immersed in an aqueous electrolyte, which have severely limited mass transport across the electrolyte and hydrodynamic boundary layer. To avoid these limitations alkaline flow cells with a gas diffusion electrode (GDE) operated in a flow-by mode are sometimes used to achieve more realistic conditions. Although they provide higher current densities (CD) and energy efficiencies (EE), they suffer from carbonate salt precipitation in the stagnant pores of the GDE, moreover in KOH electrolyte CO_2 is parasitically converted to bicarbonate. To remedy the latter problem neutral electrolytes, such as K_2SO_4 or KHCO_3, can replace alkaline electrolytes, but these have so far demonstrated low EE due to high ohmic resistance and overpotentials in the GDE.
机译:电化学二氧化碳还原反应(CO_2RR)是螯合CO_2的有希望的策略,同时合成有价值的化学品,利用来自太阳能和风能的间歇可再生能源供应。通常在H细胞中研究电解,其由浸入水性电解质中的平面电极组成,其在电解质和流体动力边界层上具有严重限制的质量传输。为了避免这些限制,有时用于在流动模式下操作的气体扩散电极(GDE)的碱性流动细胞用于实现更现实的条件。虽然它们提供更高的电流密度(CD)和能量效率(EE),但它们在GDE的停滞孔中遭受碳酸盐盐沉淀,而在KOH电解质CO_2中则寄生转化为碳酸氢盐。为了补救后一种问题中性电解质,例如K_2SO_4或KHCO_3,可以代替碱性电解质,但到目前为止,由于GDE中的高欧姆抗性和过电位,这些迄今为止已经证明了低EE。

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