二氧化碳加氢制高附加值化学品的多相催化体系。
Heterogeneous Catalytic Systems for Carbon Dioxide Hydrogenation to Value-Added Chemicals.
机构信息
Department of Chemical and Process Engineering, University of Canterbury, Christchurch, New Zealand.
School of Physical and Chemical Sciences, University of Canterbury, Christchurch, New Zealand.
出版信息
Chempluschem. 2023 Jul;88(7):e202300157. doi: 10.1002/cplu.202300157.
Utilizing renewable energy to hydrogenate carbon dioxide into fuels eliminates massive CO emissions from the atmosphere and diminishes our need for using fossil fuels. This review presents the most recent developments for designing heterogeneous catalysts for the hydrogenation of CO to formate, methanol, and C hydrocarbons. Thermodynamic challenges and mechanistic insights are discussed, providing a strong foundation to propose a suitable catalyst. The main body of this review focuses on nanostructured catalysts for constructing efficient heterogeneous systems. The most important factors affecting catalytic performance are highlighted, including active metals, supports and promoters that can potentially be used. The summary of the results and the outlook are presented in the final section. During the past few decades, heterogeneous CO hydrogenation has gained much attention and made tremendous progress. Thus, many highly efficient catalysts have been studied to discover their active sites and provide mechanistic insights. This paper summarizes recent advances in CO hydrogenation and its conversion into various hydrocarbons such as formate, methanol, and C products. As for formate production, Au and Ru nanocatalysts show superior activity. However, considering the catalyst cost, Cu-based catalysts have an excellent prospect for methanol production, among other catalysts. Ultra-small nanoparticles and nanoclusters appear promising to provide highly active cost-effective catalysts. A growing number of researchers are investigating the possibility of directly synthesizing C products through CO hydrogenation. The major challenge in producing heavy hydrocarbons is breaking the ASF limitations, which have been achieved over bifunctional catalysts using zeolites. Using suitable support and promoter can lead to a superior activity, ascribed to structural, electronic, and chemical promotional effects.
利用可再生能源将二氧化碳加氢转化为燃料,可以消除大气中大量的 CO 排放,减少我们对化石燃料的依赖。本综述介绍了用于设计将 CO 加氢为甲酸盐、甲醇和 C 烃的多相催化剂的最新进展。讨论了热力学挑战和反应机理的见解,为提出合适的催化剂提供了坚实的基础。本综述的主要内容集中在用于构建高效多相体系的纳米结构催化剂上。强调了影响催化性能的最重要因素,包括可能使用的活性金属、载体和促进剂。在最后一节中给出了结果的总结和展望。在过去的几十年中,多相 CO 加氢得到了广泛关注,并取得了巨大进展。因此,研究了许多高效催化剂以发现其活性位点并提供反应机理的见解。本文总结了 CO 加氢及其转化为各种烃类,如甲酸盐、甲醇和 C 产物的最新进展。对于甲酸盐的生产,Au 和 Ru 纳米催化剂表现出优异的活性。然而,考虑到催化剂成本,Cu 基催化剂在甲醇生产等方面具有极好的前景。超小纳米颗粒和纳米团簇似乎有望提供高活性、经济高效的催化剂。越来越多的研究人员正在研究通过 CO 加氢直接合成 C 产物的可能性。生产重质烃类的主要挑战是打破 ASF 限制,这已经在使用沸石的双功能催化剂上实现。使用合适的载体和促进剂可以提高活性,这归因于结构、电子和化学促进作用。