三吡啶
堆积
光催化
配体(生物化学)
催化作用
超分子化学
光化学
猝灭(荧光)
光致发光
超分子组装
量子产额
金属
材料科学
化学
结晶学
荧光
晶体结构
有机化学
生物化学
受体
物理
光电子学
量子力学
冶金
作者
Youting Fang,Ting Liu,Longxin Chen,Duobin Chao
标识
DOI:10.1021/acscatal.2c04845
摘要
Coordination-driven metallo-supramolecular assemblies are potentially efficient catalysts in photocatalytic CO2 reduction. However, the relationship between morphology and photocatalytic performance remains barely explored. In this work, three metallo-supramolecular assemblies composed of Zn2+ and a flexible tris(terpyridine) ligand have been prepared for noble metal-free CO2 photoreduction on the basis of metal–ligand coordination, hydrogen bonding, and π–π stacking. The three assemblies possess distinct self-assembled morphologies including spherical particle, fibrous-like gel, and microrod. It has been found that the fibrous-like gel exhibits the best catalytic performance in photoreduction of CO2 to CO with a yield of 6.3 mmol g–1 h–1 and 94.7% selectivity over H2 generation. Photoelectrochemical measurements, photoluminescence quenching experiments, and UV–vis absorption spectroscopy studies have demonstrated that the ligand-based electron transfer of the gel is more efficient compared with the other two assemblies.
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