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单原子Pd/α-MoC催化剂上糠醛在温和条件下的选择性加氢

Selective Hydrogenation of Furfural Under Mild Conditions Over Single-Atom Pd/α-MoC Catalyst.

作者信息

Liu Ziyue, Chen Xiaoli, Luo Mi, Jiang Qian, Li Xinyue, Yang Chengmei, Zhang Qi, Ma Longlong, Yan Long

机构信息

Department of Thermal Science and Energy Engineering, University of Science and Technology of China, Hefei, 230026, PR China.

CAS Key Laboratory of Renewable Energy, Guangdong Provincial Key Laboratory of New and Renewable Energy Research and Development, Guangzhou Institute of Energy Conversion, Chinese Academy of Sciences, Guangzhou, 510640, PR China.

出版信息

ChemSusChem. 2025 Apr 1;18(7):e202401802. doi: 10.1002/cssc.202401802. Epub 2024 Nov 10.

DOI:10.1002/cssc.202401802
PMID:39385700
Abstract

The selective activation of C=O bonds was the key challenge in the field of biomass utilization. Researchers worked on this purpose by developing high-active and high-selective catalysts. In this study, a Pd/α-MoC single-atom catalyst was synthesized and applied in selective hydrogenation of biomass-derived furfural with 96.7 % conversion and 92.4 % selectivity under a near-room temperature. With various characterizations, the formation of Pd single-atom sites over the surface of α-MoC was confirmed. Then, the dominant structure of Pd single-atom site and the reaction pathway were proposed with experimental and Density Functional Theory (DFT) studies. Compared with undecorated α-MoC, the introduction of Pd single-atom species significantly altered the reaction mechanism from Meerwein-Ponndorf-Verley (MPV) process. Moreover, the Pd single-atoms loading on α-MoC(111) surface notably reduced the energy barriers of H activation and C=O bond hydrogenation, which may lead to the improving catalytic performance of α-MoC based catalyst. Hence, this investigation could provide a new strategy and understanding for the development of high-active and low-cost catalysts.

摘要

C=O键的选择性活化是生物质利用领域的关键挑战。研究人员致力于通过开发高活性和高选择性催化剂来实现这一目标。在本研究中,合成了一种Pd/α-MoC单原子催化剂,并将其应用于生物质衍生糠醛的选择性加氢反应,在近室温条件下,糠醛转化率为96.7%,选择性为92.4%。通过各种表征手段,证实了α-MoC表面形成了Pd单原子位点。然后,通过实验和密度泛函理论(DFT)研究,提出了Pd单原子位点的主导结构和反应途径。与未修饰的α-MoC相比,Pd单原子物种的引入显著改变了反应机理,从迈尔外因-彭多夫-韦利(MPV)过程转变。此外,Pd单原子负载在α-MoC(111)表面显著降低了H活化和C=O键加氢的能垒,这可能导致基于α-MoC的催化剂催化性能的提高。因此,本研究可为开发高活性和低成本催化剂提供新的策略和认识。

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