Key Laboratory of Chemical Additives for China National Light Industry School of Chemistry and Chemical Engineering, Shaanxi University of Science and Technology, Xi'an, 710021, P. R. China.
School of Environmental Science and Engineering, Shaanxi University of Science and Technology, Xi'an, 710021, P. R. China.
Chemistry. 2022 Dec 27;28(72):e202201992. doi: 10.1002/chem.202201992. Epub 2022 Nov 8.
CoFeO nanosheets were synthesized by a facile coprecipitation and calcination method. The effect of calcination temperature on the crystal texture, morphology and surface areas of CoFeO were fully explored. CoFeO sample calcined at 600 °C (CoFeO -600) showed superior catalytic performance for the reduction of CO under visible light. Compared with the pure Ru(bpy) -sensitized CO reduction system, the CoFeO -added system achieved 19-fold enhancement of CO production (45.7 μmol/h). The mixed valence state and nanosheet-like structure of CoFeO cocatalyst support its ultra-high charge transfer and abundant CO active adsorption sites exposure, which promote the separation of photogenerated charges, and thus improve the photocatalytic CO reduction activity. Carbon source of CO from CO was verified by CO isotopic labelling experiment. Repeated activity experiments confirmed the good stability of CoFeO in the CO photoreduction system. This work would provide prospective insights into developing novel cost-effective, efficient, and durable non-precious metal cocatalysts to improve the efficiency of photocatalytic reduction of CO .
CoFeO 纳米片通过简便的共沉淀和煅烧方法合成。充分探讨了煅烧温度对 CoFeO 的晶体结构、形态和表面积的影响。在 600°C 下煅烧的 CoFeO 样品(CoFeO-600)在可见光下对 CO 的还原表现出优异的催化性能。与纯 Ru(bpy)敏化的 CO 还原体系相比,添加 CoFeO 的体系的 CO 产量提高了 19 倍(45.7 μmol/h)。CoFeO 助催化剂的混合价态和纳米片状结构支持其超高的电荷转移和丰富的 CO 活性吸附位暴露,这促进了光生电荷的分离,从而提高了光催化 CO 还原活性。通过 CO 同位素标记实验验证了 CO 作为 CO 来源的碳源。重复活性实验证实了 CoFeO 在 CO 光还原体系中的良好稳定性。这项工作将为开发新型经济高效、耐用的非贵金属助催化剂提供有前景的见解,以提高 CO 光催化还原的效率。