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    MnOx、FeOx和CuOx基核壳催化剂在NH3-SCR脱硝中的研究进展

    Research progress of MnOx-, FeOx- and CuOx-based core-shell catalysts in NH3-SCR denitrification

    • 摘要: 为改善氨选择性催化还原(NH3-SCR)脱硝催化剂的低温活性与抗中毒性能,本文综述了MnOx、FeOx和CuOx基核壳催化剂的研究进展。通过系统分析核壳结构的设计策略,重点探讨了壳层包覆在保护活性位点、调控氧化还原性能以及增强界面协同作用方面的机制。研究表明,催化剂性能的提升主要归因于壳层结构对硫酸盐沉积的抑制、氧空位的有效生成以及表面酸性的合理调控。核壳结构的引入显著提高了催化剂的低温活性,拓宽了其反应窗口,并增强了抗水和抗硫性能。核壳结构被认为是构建高性能SCR催化剂的有效途径,然而目前仍面临制备工艺复杂、抗毒持久性不足等挑战。本研究为今后开发高性能核壳催化剂提供了理论依据与技术参考。

       

      Abstract: To improve the low-temperature activity and poisoning resistance of ammonia selective catalytic reduction (NH3-SCR) denitrification catalysts, this review summarizes recent progress in the development of MnOx-, FeOx-, and CuOx-based core-shell catalysts. By systematically examining design strategies for core-shell architectures, we emphasize the role of the shell layer in protecting active sites, tuning redox properties, and enhancing interfacial synergy. The findings reveal that the performance enhancement stems mainly from the suppression of sulfate deposition, effective generation of oxygen vacancies, and rational modulation of surface acidity enabled by the shell structure. The introduction of a core-shell configuration significantly promotes low-temperature catalytic activity, widens the operating temperature window, and improves resistance to H2O and SO2. The core-shell structure is recognized as an effective strategy for constructing high-performance SCR catalysts. However, challenges such as complex synthesis procedures and insufficient long-term anti-poisoning stability still persist. This work offers a theoretical basis and technical reference for the further development of high-performance core-shell catalysts.

       

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