Ultra-small PdAuIr nanoparticles on amine-functionalized porous organic polymers for efficient dehydrogenation from FA at room temperature

被引:6
作者
Guo, Xiaosha [1 ]
Tian, Fengwu [1 ]
Tang, Tian [1 ]
Di, Xixi [1 ]
Wang, Wei [1 ]
Zhao, Zuoping [1 ,2 ]
Ji, Xiaohui [1 ]
Shao, Xianzhao [1 ]
机构
[1] Shaanxi Univ Technol, Sch Chem & Environm Sci, Shaanxi Key Lab Catalysis, Hanzhong 723001, Peoples R China
[2] Shaanxi Univ Technol, State Key Lab Qinba Bioresource & Ecol Environm, Hanzhong 723001, Peoples R China
关键词
Porous organic polymers; Formic acid dehydrogenation; PdAuIr alloy; High activity; FORMIC-ACID DECOMPOSITION; HYDROGEN GENERATION; GRAPHENE-OXIDE; CATALYST; CARBON; PD; OPPORTUNITIES; PERFORMANCE; FRAMEWORK; MIL-101;
D O I
10.1016/j.ijhydene.2023.06.188
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Formic acid (FA) is a prospective hydrogen storage agent, which has attracted much attention for its low toxicity and stability and plays a significant role in the comprehensive implementation of the hydrogen economy. In this regard, it is very important to utilize additive free FA dehydrogenation, for which few heterogeneous catalysts are available. Herein, we report ultra-small PdAuIr nanoparticles (NPs) supported on amine-based amorphous porous organic polymers (POPs), which exhibit excellent FA dehydrogenation activity with an initial total turnover number (TOF) of 9635 h-1 without additives at room temperature and apparent activation energy (Eaapp) of 36.5 kJ/mol. The results show that the excellent performance can be attributed to the synergistic effect of trimetallic alloys and strong metal-support interaction effect (SMSI), as well as to the amine groups (-NH2) grafted on POPs which facilitates the O-H bond splitting on FA. Overall, the simple and efficient synthetic strategy provides a new method for the selective dehydrogenation of FA.(c) 2023 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:38708 / 38718
页数:11
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