使用增强型可见光驱动的非均相光催化CO2甲烷化Cu2O@Cu-MOF-74薄膜

Hao Wu , Wahyu Prasetyo Utomo , Yuanmeng Tian , Chun Hong Mak , Hoi Ying Chung , Hsien-Yi Hsu , Jin Shang , Yun Hau Ng
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引用次数: 2

摘要

氧化亚铜是一种潜在的用于还原CO2的光催化剂。然而,其高电荷复合率和低吸附CO2的能力限制了其活性,特别是当使用气态CO2时。本文采用拓扑变换方法将具有高CO2吸附性的Cu基金属有机骨架(Cu-MOF-74)涂覆在Cu2O纳米线上。优化后的Cu2O@Cu-MOF-74在可见光照射(>;420nm)下,以水蒸气为电子供体的复合薄膜显示出比裸Cu2O高4.5倍的CH4析出速率。电化学阻抗谱、瞬态光电流测量和荧光光谱的分析结果共同表明,用Cu-MOF-74修饰Cu2O有助于从激发的Cu2O中提取电子,从而诱导用于还原CO2的长寿命光电荷。这项研究通过在过渡金属氧化物表面涂覆金属有机框架来对其进行改性,以应用于光催化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Enhanced visible-light-driven heterogeneous photocatalytic CO2 methanation using a Cu2O@Cu-MOF-74 thin film

Cuprous oxide is a potential photocatalyst for the reduction of CO2. However, its high rate of charge recombination and low ability to adsorb CO2 limit its activity, particularly when gaseous CO2 was used. Herein, a Cu-based metal-organic framework (Cu-MOF-74) with high CO2 adsorption is coated onto Cu2O nanowires by a topotactic transformation method. The optimized Cu2O@Cu-MOF-74 composite thin film showed a CH4 evolution rate 4.5 times higher than that of bare Cu2O under visible light illumination (>420 nm), with water vapor as the electron donor. Analysis results of electrochemical impedance spectroscopy, transient photocurrent measurements, and fluorescence spectroscopy collectively suggest that the decoration of Cu2O with Cu-MOF-74 facilitates electron extraction from excited Cu2O, thereby inducing long-lived photocharges for the reduction of CO2. This study provides insights into the modification of transition metal oxides for application in photocatalysis by coating the surface with metal-organic frameworks.

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