Crystal facet engineering of metal oxides for upgrading biomass-derived oxygenates: a perspective

IF 3.4 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Zihao Liu, Yonghua Guo, Qingfeng Ge and Xinli Zhu
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Abstract

Coordinatively unsaturated metal cations and oxygen anions on the surface of amphoteric metal oxides serve as acid and base centers, respectively, enabling a number of acid/base-catalyzed reactions. In particular, the O atom of oxygenates can readily coordinate with surface metal cations and can therefore initiate various reactions that are important for upgrading biomass-derived oxygenates. Metal oxide catalysts prepared via conventional methods expose various facets with distinct properties, making it difficult to elucidate the reaction chemistry and mechanism mediated on metal oxides at an atomic level. Advances in synthesis of nanocrystals of metal oxides with predominantly exposing a certain facet allow one to explore the reaction chemistry on well-defined metal oxide facets under real reaction conditions and thus may provide a powerful approach to investigate the facet-dependent structure–activity relationships of metal oxide-mediated reactions. In this perspective, we first elaborated on the fine structure and properties of various facets of TiO2 and CeO2 and then surveyed the dehydration/dehydrogenation of alcohols, ketonization of carboxylic acids, and aldol condensation of ketones and aldehydes mediated by metal oxides. In particular, we discussed the relationship between catalytic performances and the facet-dependent acid–base property and fine surface geometrical structure. Finally, we described challenges and opportunities associated with future research on metal oxide-mediated reactions via crystal facet engineering.

Abstract Image

金属氧化物的晶面工程升级生物质衍生的含氧化合物:一个前景
两性金属氧化物表面的配位不饱和金属阳离子和氧阴离子分别作为酸中心和碱中心,使许多酸/碱催化反应成为可能。特别是氧合物的O原子可以很容易地与表面金属阳离子配位,因此可以引发各种反应,这些反应对于升级生物质衍生的氧合物很重要。传统方法制备的金属氧化物催化剂暴露了具有不同性质的各个方面,使得在原子水平上难以阐明金属氧化物介导的反应化学和机理。金属氧化物纳米晶体的合成进展,主要暴露某一特定面,使人们能够在真实的反应条件下探索明确定义的金属氧化物面上的反应化学,从而可能为研究金属氧化物介导反应的面依赖的结构-活性关系提供有力的方法。在这方面,我们首先阐述了TiO2和CeO2各方面的精细结构和性能,然后考察了金属氧化物介导的醇类脱水/脱氢、羧酸酮化和酮醛缩合反应。特别地,我们讨论了催化性能与面相关的酸碱性质和精细的表面几何结构之间的关系。最后,我们描述了未来通过晶面工程研究金属氧化物介导反应的挑战和机遇。
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来源期刊
Reaction Chemistry & Engineering
Reaction Chemistry & Engineering Chemistry-Chemistry (miscellaneous)
CiteScore
6.60
自引率
7.70%
发文量
227
期刊介绍: Reaction Chemistry & Engineering is a new journal reporting cutting edge research into all aspects of making molecules for the benefit of fundamental research, applied processes and wider society. From fundamental, molecular-level chemistry to large scale chemical production, Reaction Chemistry & Engineering brings together communities of chemists and chemical engineers working to ensure the crucial role of reaction chemistry in today’s world.
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