Affiliation:
1. Department of Chemical Engineering Hanyang University Seoul 04763 (Republic of Korea
2. R&D Team SK eco prime Co. Ltd. Gyeonggi-do 13494 (Republic of Korea
3. Research Institute of Industrial Science Hanyang University Seoul 04763 (Republic of Korea
Abstract
AbstractIn heterogeneous catalysis, heterolytic H2 activation for (selective) hydrogenation and hydroprocessing reactions involves the dissociation of adsorbed H2 molecules into proton (Hδ+) and hydride (Hδ−) on the catalyst surface. This approach offers several advantages, including high selectivity for polar bond (s), a low energy barrier for H2 dissociation, a high capacity for reaction‐favorable H2 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 Å between the pairs. This review highlights intrinsic catalyst properties for heterolytic H2 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 H2 activation characteristics will be significantly effective in various hydrogenation and hydroprocessing reactions.
Funder
Ministry of Higher Education and Scientific Research
Cited by
1 articles.
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