氢溢出机制的DFT洞察:金属种类、尺寸和支撑的影响

IF 3.2 3区 化学 Q2 CHEMISTRY, PHYSICAL
Cheng-Hsi Yeh, Ho Viet Thang, Yves Ira A. Reyes, Carmine Coluccini, Hsin-Yi Tiffany Chen
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引用次数: 0

摘要

氢溢出是多相催化的重要机理。本文采用密度泛函理论计算方法,利用Ru、Ni和Pt的单原子(M1)和四原子团簇(M4)模型,在锐钛矿TiO2(101)、金红石TiO2(110)、MgO(100)、MgO(110)和石墨烯上负载,研究金属-载体相互作用(MSI)和氢溢出机制,包括金属尺寸、金属种类和载体效应。对于M1体系,结合能(Eb)在不同的M1种类和底物表面上变化很大。与MSI受金属类型影响的M1体系相反,支持的M4模型主要由支撑物决定:r-TiO2(110) >;a-TiO2祝辞(101);分别以(110)在分别以(100)在石墨烯。在热力学上,有利的氢溢出在氧化物支持的M1模型上需要6 ML的氢覆盖(θ),而对应的M4系统需要3 ML。因此,氧化物支持的团簇催化剂比单原子催化剂更能促进有利的氢溢出;氢向TiO2的溢出比向MgO的溢出更有利。相比之下,在石墨烯支撑的M1和M4模型上没有观察到有利的氢溢出。尽管考虑了相同的途径,但根据载体的不同,观察到不同的氢溢出机制:(1)在可还原的TiO2上,氢以质子的形式溢出,电子转移到载体上;(ii)在不可还原的氧化镁上,氢作为质子溢出,但电子仍然局限于被束缚的金属;(iii)在石墨烯上,氢以中性氢原子的形式溢出。值得注意的是,从热力学和动力学的角度来看,具有更强MSI的支撑型M4模型预计会表现出更容易的氢溢出,特别是当考虑不同支撑的相同金属种类时。这些详细的见解有望促进对催化剂氢溢出的理解,这将对未来的设计和开发有价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

DFT Insights into Hydrogen Spillover Mechanisms: Effects of Metal Species, Size, and Support

DFT Insights into Hydrogen Spillover Mechanisms: Effects of Metal Species, Size, and Support
Hydrogen spillover is a crucial mechanism in heterogeneous catalysis. Herein, density functional theory calculations were conducted to study the metal–support interactions (MSI) and the hydrogen spillover mechanisms in terms of metal size, metal species, and support effects using single-atom (M1) and four-atom cluster (M4) models of Ru, Ni, and Pt, supported on anatase TiO2(101), rutile TiO2(110), MgO(100), MgO(110), and graphene. For M1 systems, the binding energies (Eb) vary widely across different M1 species and substrate surfaces. In contrast to M1 systems whose MSI are affected by metal type, those supported M4 models are determined primarily by the support: r-TiO2(110) > a-TiO2(101) > MgO(110) > MgO(100) > graphene. Thermodynamically favorable hydrogen spillover on oxide-supported M1 models required hydrogen coverages (θ) of ∼6 ML, whereas counterpart M4 systems require ∼3 ML. Therefore, oxide-supported cluster catalysts can facilitate favorable hydrogen spillover better than single-atom catalysts; hydrogen spillover to TiO2 is more favorable than to MgO. In contrast, no favorable hydrogen spillover was observed on graphene-supported M1 and M4 models. Despite considering the same route, different hydrogen spillover mechanisms are observed depending on the support: (i) on reducible TiO2, hydrogen spills over as a proton with the electron transferred to the support; (ii) on nonreducible MgO, hydrogen spills over as a proton but the electron remains localized to the bound metal; (iii) on graphene, hydrogen spills over as a neutral hydrogen atom. Notably, supported M4 models with stronger MSI are predicted to exhibit a more facile hydrogen spillover from both thermodynamic and kinetic perspectives, particularly when considering the same metal species across different supports. These detailed insights are expected to advance the understanding of hydrogen spillover on catalysts, which will be valuable for their future design and development.
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来源期刊
The Journal of Physical Chemistry C
The Journal of Physical Chemistry C 化学-材料科学:综合
CiteScore
6.50
自引率
8.10%
发文量
2047
审稿时长
1.8 months
期刊介绍: The Journal of Physical Chemistry A/B/C is devoted to reporting new and original experimental and theoretical basic research of interest to physical chemists, biophysical chemists, and chemical physicists.
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