在可见光照射下使用磷化镍负载 CdS 光催化还原二氧化碳至合成气

Poonam Yadav, Santosh Kumar, Nandhakumar Velankanni, Thomas D Kühne, Suresh Gosavi, R. Raghupathy, R. Bhosale, Georg Held, M. Shelke, Satishchandra B Ogale
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摘要

光催化二氧化碳还原是生产合成气(H2 + CO)的一种可持续途径,而合成气是在工业规模上生产许多重要液体燃料的关键原料。然而,实现合成气中 H2:CO 的适当可调比例以达到商业目的是一项具有挑战性的任务。在这项工作中,我们提出了一种低成本、非贵金属、基于磷化物的助催化剂--Ni2P负载CdS光催化剂系统,用于光催化还原二氧化碳。作为助催化剂,Ni2P 可有效分离 CdS 中产生的光激发电荷,从而产生合成气。3 wt.% 的 CdS/Ni2P 表现出卓越的性能,在合成气成分 H2:CO 比率为 2 到 4 的情况下,CO 演化率为 50.6 µmol/g/h ,H2 演化率为 115 µmol/g/h 。此外,我们还进行了第一原理密度泛函理论(DFT)计算,以研究催化剂体系的表面能效,结果发现与我们的实验发现一致。事实上,与纯表面相比,复合材料更有利于将 CO2 光还原成合成气。
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Photocatalytic CO2 reduction to syngas using nickel phosphide loaded CdS under visible light irradiation
Photocatalytic CO2 reduction is a sustainable pathway to produce syngas (H2 + CO) which is a key feed stock for the production of many important liquid fuels on the industrial scale. However, achieving appropriate tunable ratio of H2:CO in syngas for commercial purpose is a challenging task. In this work, we present a low cost and non-noble metal, phosphide based co-catalyst - Ni2P loaded CdS photocatalyst system for the photocatalytic CO2 reduction. Ni2P as a co-catalyst fosters efficient charge separation of photoexcited charges generated in CdS producing syngas. 3 wt.% CdS/Ni2P exhibited exceptional performance of 50.6 µmol/g/h of CO evolution rate and 115 µmol/g/h of H2 evolution rate with a syngas composition varying from 2 to 4 in H2:CO ratio. Further, the first-principles density functional theory (DFT) calculations were performed to study surface energetics of the catalyst system and the results are found to be consistent with our experimental findings. Indeed, they establish that the composite favors the CO2 photoreduction into syngas more efficiently as compared to pure surfaces.
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