Efficient hydrolytic dehydrogenation of ammonia borane over ultrafine Ru nanoparticles supported on biomass-derived porous carbon

被引:30
|
作者
Li, Shuai-Hui [1 ,2 ]
Song, Xing-Rui [2 ]
Li, Yong-Ting [2 ]
Zhao, Ying-Qiang [3 ]
Zheng, Xiu-Cheng [2 ,4 ]
机构
[1] Zhengzhou Univ, Henan Prov Peoples Hosp, Peoples Hosp, Zhengzhou 450003, Peoples R China
[2] Zhengzhou Univ, Coll Chem, Green Catalysis Ctr, Zhengzhou 450001, Peoples R China
[3] Shandong Normal Univ, Coll Chem Chem Engn & Mat Sci, Jinan 250014, Peoples R China
[4] Nankai Univ, Key Lab Adv Energy Mat Chem, Minist Educ, Coll Chem, Tianjin 300071, Peoples R China
基金
中国国家自然科学基金;
关键词
Ultrafine Ru nanoparticles; Cattail fiber biomass; Hierarchical porous carbon; Ammonia borane hydrolysis; Hydrogen generation; MONODISPERSE RUTHENIUM NANOPARTICLES; REDUCED GRAPHENE OXIDE; HYDROGEN GENERATION; FACILE SYNTHESIS; SODIUM-BOROHYDRIDE; PT/CNT CATALYSTS; H-2; GENERATION; EVOLUTION; NANOSHEETS; INSIGHTS;
D O I
10.1016/j.ijhydene.2021.06.029
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
Ammonia borane hydrolysis is a promising strategy for developing sustainable hydrogen energy. However, this reaction is not kinetically feasible at ambient temperature, thus developing a proper catalyst is indispensable. In this work, Porous carbon is facilely prepared from cattail fibers by using K2CO3, and then used to stabilize Ru nanoparticles. The effects of different synthesis parameters for the biomass-derived carbon supports (e. g. K2CO3 dosage and calcination temperature) and various catalytic reaction conditions (e. g. the amounts of the catalysts, ammonia borane and NaOH, and reaction temperature) on the hydrolysis rate of ammonia borane are investigated. Benefitting from the interconnected hierarchical pores of the optimal porous carbon (p-C), which was prepared with a mass ratio of 6 : 1 for K2CO3 to cattail fibers and calcined at 873 K, and the high dispersion of Ru nanoparticles, the optimal Ru/p-C catalysts exhibit excellent catalytic performance. The corresponding apparent activation energy (28.8 kJ mol(-1)) and turnover frequency 744.7 min(-1) in alkaline solution) are superior to many catalysts previously reported. This work offers a competitive catalyst for the hydrolytic dehydrogenation of chemical hydrogen storage materials. (C) 2021 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:27555 / 27566
页数:12
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