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水稳定的铜基金属有机框架纳米带实现选择性一氧化碳光还原

Selective CO Photoreduction Enabled by Water-stable Cu-based Metal-organic Framework Nanoribbons.

作者信息

Zhao Yuan, Chen Runhua, Luo Jingchen, Zhu Juncheng, Wu Yang, Qiao Panzhe, Yan Wensheng, Pan Yang, Zhu Junfa, Zu Xiaolong, Sun Yongfu

机构信息

Hefei National Research Center for Physical Sciences at Microscale, National Synchrotron Radiation Laboratory, University of Science and Technology of China, Hefei, Anhui, 230026, P. R. China.

Shanghai Synchrotron Radiation Facility, Shanghai Advanced Research Institute, Chinese Academy of Sciences, Shanghai, 201204, P. R. China.

出版信息

Chemphyschem. 2024 Mar 1;25(5):e202300368. doi: 10.1002/cphc.202300368. Epub 2024 Jan 26.

Abstract

The goal of photocatalytic CO reduction system is to achieve near 100 % selectivity for the desirable product with reasonably high yield and stability. Here, two-dimensional metal-organic frameworks are constructed with abundant and uniform monometallic active sites, aiming to be an emerged platform for efficient and selective CO reduction. As an example, water-stable Cu-based metal-organic framework nanoribbons with coordinatively unsaturated single CuII sites are first fabricated, evidenced by X-ray diffraction patterns and X-ray absorption spectroscopy. In situ Fourier-transform infrared spectra and Gibbs free energy calculations unravel the formation of the key intermediate COOH* and CO* is an exothermic and spontaneous process, whereas the competitive hydrogen evolution reaction is endothermic and non-spontaneous, which accounts for the selective CO reduction. As a result, in an aqueous solution containing 1 mol L KHCO and without any sacrifice reagent, the water-stable Cu-based metal-organic framework nanoribbons exhibited an average CO yield of 82 μmol g  h with the selectivity up to 97 % during 72 h cycling test, which is comparable to other reported photocatalysts under similar conditions.

摘要

光催化CO还原系统的目标是在具有合理高产量和稳定性的情况下,实现对所需产物接近100%的选择性。在此,构建了具有丰富且均匀单金属活性位点的二维金属有机框架,旨在成为高效且选择性CO还原的新兴平台。例如,首先制备了具有配位不饱和单CuII位点的水稳定铜基金属有机框架纳米带,这通过X射线衍射图谱和X射线吸收光谱得到证实。原位傅里叶变换红外光谱和吉布斯自由能计算揭示了关键中间体COOH和CO的形成是一个放热且自发的过程,而竞争性析氢反应是吸热且非自发的,这解释了选择性CO还原的原因。结果,在含有1 mol L KHCO且无任何牺牲试剂的水溶液中,水稳定铜基金属有机框架纳米带在72 h循环测试期间表现出平均CO产量为82 μmol g  h,选择性高达97%,这与在类似条件下其他报道的光催化剂相当。

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