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    CO2加氢制甲醇非贵金属催化剂研究进展与展望

    Research advances and prospects of non-noble metal catalysts for CO2 hydrogenation to methanol

    • 摘要: 人为CO2排放激增引发的环境危机加速了碳中和技术的发展,其中CO2加氢制甲醇因兼具碳减排、绿氢储能与高附加值化学品转化潜力备受关注,但其工业化应用受限于高效催化剂的开发与反应机制的深入解析。围绕具有良好工业前景的非贵金属催化体系,系统综述其热力学路径、催化剂设计与反应机理的最新进展。研究指出,Cu基催化剂通过活性位优化与界面工程显著提升活性位点密度与氧空位再生能力;In2O3基催化剂因高氧空位稳定性与抗烧结特性展现优异性能;Zr基固溶体催化剂则通过晶格应力与氧空位协同作用效应优化电子结构,突破单组分性能瓶颈。此外,载体比表面积与路易斯酸碱位、助剂的选择及其电子转移功能以及制备策略对金属活性位的精准调控,被证实为关键优化方向。反应机理层面,实验与理论计算揭示甲酸盐路径(*HCOO主导)与逆水煤气变换–羰基化路径(*COOH解离)的竞争机制,具体主导机制与催化剂结构特性密切相关。本综述通过多维度整合催化剂设计、表界面特性、反应性能与动力学行为的关联性研究,为构建新型高效CO2制甲醇体系的开发提供理论支撑,推动碳循环技术与绿氢经济的深度融合,对碳中和目标下能源−环境协同技术发展具有重要参考价值。

       

      Abstract: The environmental crisis triggered by the dramatic surge in anthropogenic CO2 emissions has accelerated the development of carbon neutrality technologies. Among these, CO2 hydrogenation to methanol has garnered significant attention due to its triple potential for carbon emission reduction, green hydrogen energy storage, and high-value-added chemical conversion. However, its industrial application remains constrained by the development of efficient catalysts and comprehensive understanding of reaction mechanisms. This review systematically focuses on non-noble metal catalytic systems with promising industrial prospects, summarizing the latest advances in their thermodynamic pathways, catalyst material design, and reaction mechanisms. Key findings reveal that Cu-based catalysts demonstrate enhanced active site density and oxygen vacancy regeneration through optimized active site configuration and interface engineering. In2O3-based catalysts exhibit superior performance owing to their exceptional oxygen vacancy stability and anti-sintering characteristics. Zr-based solid solution catalysts, meanwhile, optimize electronic structures via the synergistic effect of lattice stress and oxygen vacancies, overcoming the performance limitations of single-component catalysts. Moreover, key optimization directions have been identified: specific surface area and Lewis acid-base sites of supports, selection of promoters and their electron transfer functions, and preparation strategies for precise regulation of metallic active sites. Mechanistic studies combining experimental and theoretical approaches unveil a competitive relationship between the formate pathway (dominated by *HCOO intermediates) and the reverse water-gas shift-carbonylation pathway (governed by *COOH dissociation), with pathway dominance strongly correlated to catalyst structural characteristics. By integrating multiscale catalyst design with interfacial properties and kinetic behavior analysis, this review provides theoretical guidance for constructing efficient CO2-to-methanol conversion systems. It advances the integration of carbon cycling technologies with green hydrogen economy, offering valuable insights for developing energy-environment synergistic technologies under carbon neutrality objectives.

       

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