Xin Cao , Chun-Yu Liu , Yuming Dong , Tingyu Yang , Xinying Chen , Yongfa Zhu
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引用次数: 0
摘要
铜基催化剂一直被认为是太阳能催化还原二氧化碳为高附加值化学品的最有前途的候选催化剂,但其催化性能在精确构建铜催化活性位点方面遇到了内在限制。本研究以定义明确的 Cu2Cl2-bpy(bpy = 4,4′-联吡啶)为前驱体,在聚合氮化碳(DAS-Cu@PCN)上制备了双原子位点 Cu 光催化剂,双 Cu 原子间距为 2.8 Å。我们的研究结果为原子精确光催化剂的设计提供了宝贵的指导,有助于将二氧化碳高效光催化转化为高附加值的碳产品。
Dual-atom-site Cu@PCN photocatalyst selectively produces ethane from CO2 reduction†
Copper-based catalysts have been considered as the most promising candidates in the solar-driven catalytic reduction of CO2 to value-added chemicals, but their catalytic performance encounters intrinsic limitations in the precise construction of copper catalytic active sites. This work employed the well-defined Cu2Cl2-bpy (bpy = 4,4′-bipyridine) as the precursor and fabricated a dual atom site Cu photocatalyst on polymeric carbon nitride (DAS-Cu@PCN) with a distance between dual Cu atoms of ∼2.8 Å. The PCN substrate enhances the stability of double Cu catalytic sites, and the appropriate Cu–Cu spacing effectively promotes the C–C coupling, which greatly improves the performance of photocatalytic CO2 reduction. Our findings provide valuable guidelines for the atom precise photocatalyst design toward highly efficient photocatalytic CO2 conversion to high value-added carbon products.
期刊介绍:
A multidisciplinary journal focusing on cutting edge research across all fundamental science and technological aspects of catalysis.
Editor-in-chief: Bert Weckhuysen
Impact factor: 5.0
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