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Photocathode functionalized with a molecular cobalt catalyst for selective carbon dioxide reduction in water

机译:用分子钴催化剂官能化的光电阴极用于选择性二氧化碳减少水中

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摘要

Artificial photosynthesis is a vibrant field of research aiming at converting abundant, low energy molecules such as water, nitrogen or carbon dioxide into fuels or useful chemicals by means of solar energy input. Photo-electrochemical reduction of carbon dioxide is an appealing strategy, aiming at reducing the greenhouse gas into valuable products such as carbon monoxide at low or without bias voltage. Yet, in such configuration, there is no catalytic system able to produce carbon monoxide selectively in aqueous media with high activity, and using earth-abundant molecular catalyst. Upon associating a p-type Cu(In,Ga)Se 2 semi-conductor with cobalt quaterpyridine complex, we herein report a photocathode complying with the aforementioned requirements. Pure carbon dioxide dissolved in aqueous solution (pH 6.8) is converted to carbon monoxide under visible light illumination with partial current density above 3?mA?cm -2 and 97% selectivity, showing good stability over time.
机译:人造光合作用是一种充满活力的研究领域,其旨在通过太阳能输入将诸如水,氮气或二氧化碳如水,氮气或二氧化碳如水,氮气或二氧化碳转化为燃料或有用的化学品。二氧化碳的光学电化学还原是一种吸引力的策略,旨在将温室气体降低到低或无偏置电压下的有价值的产品(如一氧化碳)。然而,在这种结构中,没有能够在具有高活性的含水介质中选择性地生产一氧化碳的催化系统,并使用土级分子催化剂。在将P型Cu(In,Ga)Se 2半导体与钴Quaterpyridine复合物相关联后,我们在本文中报告了符合上述要求的光电阴极。溶解在水溶液中的纯二氧化碳(pH6.8)在可见光照明下转化为一氧化碳,其部分电流密度高于3?mA = mc -2和97%的选择性,显示出良好的稳定性。

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