Zhu Zi-Hao, Wu Xin-Yu, Lu Jian-Feng, Xu Hui, Hou Sheng-Li, Zhao Jian, Liu Sui-Jun, Wen He-Rui
School of Chemistry and Chemical Engineering, Jiangxi Provincial Key Laboratory of Functional Crystalline Materials Chemistry, Jiangxi University of Science and Technology, Ganzhou 341000, P.R. China.
Guangdong Provincial Key Laboratory of Functional Supramolecular Coordination Materials and Applications, Jinan University, Guangzhou 510632, P.R. China.
Inorg Chem. 2025 Apr 28;64(16):8261-8269. doi: 10.1021/acs.inorgchem.5c00541. Epub 2025 Apr 12.
Electrochemical CO reduction reaction provides a mild avenue for resource utilization of CO. Metal-organic framework (MOF) materials are considered among the promising catalysts due to unique structural advantages. However, the catalytic performance of MOFs is hindered by poor conductivity, making it crucial to enhance the charge transfer for improved efficiency. Herein, a hybrid catalyst was constructed based on the In-based porphyrin framework (In-TCPP) and conducting MXene nanosheets for efficient CO conversion. As expected, MXene as a unique conductive support significantly improves the catalytic performance of the hybrid material, achieving a Faraday efficiency for HCOO of 94.0% with a 2.2-fold increase in the practical current density. Furthermore, a pure formic acid solution with a concentration of ca. 0.22 M was prepared via execution in a solid-state electrolyte-mediated MEA (MEA-SSE) device. Theoretical calculations and in situ ATR-FTIR spectra reveal that the introduction of MXene not only endows the hybrid material with metallic properties to facilitate charge transfer but also modulates the electronic structure to optimize the adsorption of the key intermediate *OCHO. This work enlightens the rational design of MOF-based electrocatalysts via the regulation of MXene and demonstrates the promise of the MEA-SSE device for practical CO reduction applications.
电化学CO还原反应为CO的资源利用提供了一条温和的途径。金属有机框架(MOF)材料因其独特的结构优势而被认为是有前景的催化剂之一。然而,MOF的催化性能受到导电性差的阻碍,因此增强电荷转移以提高效率至关重要。在此,基于铟基卟啉框架(In-TCPP)和导电的MXene纳米片构建了一种混合催化剂,用于高效的CO转化。正如预期的那样,MXene作为一种独特的导电载体显著提高了混合材料的催化性能,实现了94.0%的HCOO法拉第效率,实际电流密度提高了2.2倍。此外,通过在固态电解质介导的MEA(MEA-SSE)装置中运行制备了浓度约为0.22 M的纯甲酸溶液。理论计算和原位ATR-FTIR光谱表明,MXene的引入不仅赋予混合材料金属特性以促进电荷转移,还调节电子结构以优化关键中间体*OCHO的吸附。这项工作通过MXene的调控为基于MOF的电催化剂的合理设计提供了启示,并展示了MEA-SSE装置在实际CO还原应用中的前景。