使用金属间催化剂实现糠醛加氢过程中的产物控制

IF 11.3 1区 化学 Q1 CHEMISTRY, PHYSICAL ACS Catalysis Pub Date : 2024-11-06 DOI:10.1021/acscatal.4c04091
Charles J. Ward, Minda Chen, Andrew Lamkins, Claudio Ordonez, Rong Sun, Puranjan Chatterjee, Minghui Niu, Ruoyu Cui, Da-Jiang Liu, Wenyu Huang
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引用次数: 0

摘要

金属间纳米粒子(iNPs)作为一种有效的催化剂备受关注,但通过调整表面性质来诱导立体效应的影响却相对较少。在此,我们报告了在双金属催化剂中调节立体阻碍的策略,以此作为一种方法,通过改变仲金属原子的大小来改变使用 Rh 基 iNPs 的糠醛加氢反应的产物选择性。在封闭的介孔二氧化硅井(MSW)中合成了 RhGa、RhIn 和 RhBi 纳米粒子,并对其在糠醛气相氢化中的应用进行了评估。与单金属 Rh@MSW 相比,RhGa 和 RhIn iNPs 实现了产品控制,并提高了对呋喃和糠醇的选择性(90%)。在 Rh 中加入 Bi 几乎完全抑制了糠醛的转化。原位漫反射红外傅立叶变换光谱研究和基于密度泛函理论的机器学习加速分子动力学模拟显示,次生金属的特性强烈影响活性位点上的首选糠醛吸附模式,从而导致观察到的催化控制。在反应和再生条件下,RhM@MSW 催化剂的介孔二氧化硅外壳可防止 NP 聚集,在回收研究中也表现出良好的稳定性。
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Achieving Product Control in Furfural Hydrogenation Using Intermetallic Catalysts
Intermetallic nanoparticles (iNPs) have garnered much attention as effective catalysts, but the impact of tuning surface properties to induce steric effects is relatively unexplored. Here, we report on the strategy of governing steric hindrance in bimetallic catalysts as a method to alter product selectivity in furfural hydrogenation using Rh-based iNPs by varying the size of the secondary metal atoms. RhGa, RhIn, and RhBi nanoparticles were synthesized within confined mesoporous silica wells (MSWs) and assessed for the vapor-phase hydrogenation of furfural. RhGa and RhIn iNPs enable product control with an enhanced selectivity to furan and furfuryl alcohol (>90%) compared to the monometallic Rh@MSW. Adding Bi to Rh inhibits the transformation of furfural almost entirely. In situ diffuse reflectance infrared Fourier transform spectroscopy studies and density functional theory-based machine-learning accelerated molecular dynamics simulations reveal that the secondary metal’s identity strongly impacts the preferred furfural adsorption mode on the active sites, leading to the observed catalysis control. The mesoporous silica shell of the RhM@MSW catalyst provides protection against NP aggregation under reaction and regeneration conditions, as supported by good stability during recycling studies.
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来源期刊
ACS Catalysis
ACS Catalysis CHEMISTRY, PHYSICAL-
CiteScore
20.80
自引率
6.20%
发文量
1253
审稿时长
1.5 months
期刊介绍: ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels. The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.
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