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Heterolytic H2 Activation in Heterogeneous Hydrogenation/Hydroprocessing Catalysis

Authors
Kim, Tae WanKim, DongunKim, Soo HyunSuh, Young-Woong
Issue Date
Apr-2024
Publisher
Wiley - VCH Verlag GmbH & CO. KGaA
Keywords
Heterogeneous catalysis; Hydrogenation; Hydroprocessing; Heterolytic H-2 activation; Frustrated Lewis pairs
Citation
ChemCatChem, v.16, no.8, pp 1 - 10
Pages
10
Indexed
SCIE
SCOPUS
Journal Title
ChemCatChem
Volume
16
Number
8
Start Page
1
End Page
10
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/197302
DOI
10.1002/cctc.202301581
ISSN
1867-3880
1867-3899
Abstract
In heterogeneous catalysis, heterolytic H-2 activation for (selective) hydrogenation and hydroprocessing reactions involves the dissociation of adsorbed H-2 molecules into proton (H delta+) and hydride (H delta-) on the catalyst surface. This approach offers several advantages, including high selectivity for polar bond (s), a low energy barrier for H-2 dissociation, a high capacity for reaction-favorable H-2 adsorption, and reduced catalyst poisoning. This requires the construction of frustrated Lewis pairs on the catalyst surface, satisfying specific criteria, such as having an abundant quantity of Lewis pairs with steric hindrance and maintaining a certain distance of 3-5 & Aring; between the pairs. This review highlights intrinsic catalyst properties for heterolytic H-2 activation based on state-of-the-art reports. The main components necessary for this activation include supports with strong basic sites and/or oxygen vacancies, and/or metals of single atom. For this purpose, designed catalytic materials aim to strengthen the Lewis acidity and basicity, improve the polarization of Lewis pairs, enrich oxygen vacancies, maximize the interfacial area between metal species and Lewis base, and enhance metal-support interaction. Therefore, heterogeneous catalysts retaining such heterolytic H-2 activation characteristics will be significantly effective in various hydrogenation and hydroprocessing reactions.
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