首页|Pt基团簇催化剂设计策略在丙烷脱氢中的研究进展

Pt基团簇催化剂设计策略在丙烷脱氢中的研究进展

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丙烷脱氢制丙烯(PDH)技术作为一种高效的丙烯生产途径,具备满足全球日益增长丙烯需求的潜力.然而,PDH反应的高吸热性限制了平衡转化,即便是高活性和高选择性的Pt基催化剂在高温条件下也会由于烧结和结焦问题而失活,进而影响催化剂的稳定性和寿命.综述了 Pt基团簇催化剂的几何结构和电子特性对催化性能的影响,探讨了提升Pt基团簇稳定性的设计策略.还总结了从传统液相合成、后处理技术到原子层沉积(ALD)等方法在调控Pt基催化剂结构及抑制失活方面的最新进展.最后,展望了通过ALD技术设计结构明确的Pt基催化剂的潜力,以深入理解催化剂活性位点的性质,并探讨在分子筛限域中进一步稳定Pt基团簇的可能性.这些研究方向为开发新一代高效、稳定的PDH催化剂提供了新的思路与启示.
Advances in Pt-based cluster catalyst design strategies for propane dehydrogenation
Propane dehydrogenation(PDH)technology presents an efficient route to meet the increasing global de-mand for propylene.However,the high endothermic nature of the PDH reaction limits equilibrium conversion,and even highly active and selective Pt-based catalysts are prone to deactivation at elevated temperatures due to sintering and coking,affecting their stability and lifespan.how the geometric structure and electronic properties of Pt-based cluster catalysts impact their catalytic performance was examined and strategies to enhance the stability of these clusters was discussed.recent advancements in controlling the structure of Pt-based catalysts was summarized and preventing deactivation through various approaches,including traditional liquid-phase synthesis,post-processing techniques,and atomic layer deposition(ALD).Additionally,highlight future research directions focusing on desig-ning well-defined Pt-based catalysts with ALD technology,aiming to gain a deeper understanding of active site char-acteristics and exploring methods to further stabilize Pt clusters within molecular sieve-constrained environments.These insights provide new perspectives for developing the next generation of efficient and stable PDH catalysts.

propane dehydrogenationPt-based catalystsclusteratomic layer depositionconfinement effect

单斌、徐洁、杜纯、陈蓉、戴云生

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华中科技大学材料科学与工程学院,湖北武汉 430074

华中科技大学机械科学与工程学院,湖北武汉 430074

稀贵金属综合利用新技术国家重点实验室,云南 昆明 650106

丙烷脱氢 Pt基催化剂 团簇 原子层沉积 限域

云南贵金属实验室重大科技专项

YPML-2023050205

2024

金属功能材料
中国钢研科技集团有限公司 中国金属学会功能材料分会

金属功能材料

CSTPCD
影响因子:0.527
ISSN:1005-8192
年,卷(期):2024.31(5)