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ZSM-5中受限铜单原子用于光催化苯羟基化制苯酚

Confined Cu Single Sites in ZSM-5 for Photocatalytic Hydroxylation of Benzene to Phenol.

作者信息

Zhang Jinwen, Ding Hongxin, Hui Hehua, Yao Qingying, Feng Wenhua, Chen Tian-Xiang, Lo Tsz Woon Benedict, Ren Yuanhang, Ye Lin, Yue Bin, He Heyong

机构信息

Department of Chemistry and Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai, 200438, China.

Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hong Kong, 999077, China.

出版信息

Small. 2024 Dec;20(49):e2405150. doi: 10.1002/smll.202405150. Epub 2024 Sep 20.

Abstract

Zeolites with band-like charge transport properties have exhibited their potential activities in sensing, optics, and electronics. Herein, a precisely designed Cu@ZSM-5 catalyst is presented with an ultra-wide bandgap of 4.27 eV, showing excellent photocatalytic activity in hydroxylation of benzene with benzene conversion 27.9% and phenol selectivity 97.6%. The SXRD and Rietveld refinement results illustrate that Cu@ZSM-5 has an average of 0.8 Cu atoms per unit cell and the single Cu atoms located in the cross-section of the sinusoidal and straight channels. XANES and EXAFS further demonstrate that the Cu atoms have an oxidation state of +2, coordinated with three O atoms and one ─OH group. Detailed characterizations demonstrate that the Cu@ZSM-5 with tailored bandgap is able to enhance the photoinduced electron-hole separation and hence promote selective hydroxylation of benzene to phenol via the superoxide radical route. This work may open a new way for designing electrically conductive zeolite-supported photocatalysts.

摘要

具有带状电荷传输特性的沸石在传感、光学和电子学领域展现出了潜在活性。在此,我们展示了一种精确设计的Cu@ZSM-5催化剂,其具有4.27 eV的超宽带隙,在苯的羟基化反应中表现出优异的光催化活性,苯转化率为27.9%,苯酚选择性为97.6%。SXRD和Rietveld精修结果表明,Cu@ZSM-5每个晶胞平均含有0.8个铜原子,单个铜原子位于正弦形和直通道的横截面中。XANES和EXAFS进一步证明,铜原子的氧化态为+2,与三个氧原子和一个羟基配位。详细表征表明,具有定制带隙的Cu@ZSM-5能够增强光生电子-空穴分离,从而通过超氧自由基途径促进苯选择性羟基化为苯酚。这项工作可能为设计导电沸石负载型光催化剂开辟一条新途径。

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