Effect of Ni/tubular g-C3N4 on hydrogen storage properties of MgH2

被引:55
作者
Li, Xinjun [2 ]
Fu, Yaokun [2 ]
Xie, Yichao [2 ]
Cong, Lian [2 ]
Yu, Han [2 ]
Zhang, Lu [1 ,2 ]
Li, Yuan [1 ,2 ]
Han, Shumin [1 ,2 ]
机构
[1] Yanshan Univ, State Key Lab Metastable Mat Sci & Technol, Qinhuangdao 066004, Hebei, Peoples R China
[2] Yanshan Univ, Sch Environm & Chem Engn, Hebei Key Lab Appl Chem, Qinhuangdao 066004, Hebei, Peoples R China
基金
中国国家自然科学基金;
关键词
Hydrogen storage materials; Magnesium hydride; NI/tubular g-C3N4; Cycle stability; MAGNESIUM HYDRIDE; SYNERGETIC CATALYSIS; NANOPARTICLES; PERFORMANCE; SORPTION; CO; DEHYDROGENATION; NANOSTRUCTURES; NANOTUBES; PALLADIUM;
D O I
10.1016/j.ijhydene.2021.07.166
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
Additive doping is one of the effective methods to overcome the shortcomings of MgH2 on the aspect of relatively high operating temperatures and slow desorption kinetics. In this paper, hollow g-C3N4 (TCN) tubes with a diameter of 2 1.tm are synthesized through the hydrothermal and high-temperature pyrolysis methods, and then nickel is chemically reduced onto TCN to form Ni/TCN composite at 278 K. Ni/TCN is then introduced into the MgH2/Mg system by means of hydriding combustion and ball milling. The MgH2-Ni/TCN composite starts to release hydrogen at 535 K, which is 116 K lower than the as-milled MgH2 (651 K). The MgH2-Ni/TCN composite absorbs 5.24 wt% H-2 within 3500 s at 423 K, and takes up 3.56 wt% H-2 within 3500 s, even at a temperature as low as 373 K. The apparent activation energy (E-a) of the MgH2 decreases from 161.1 to 82.6 kJ/mol by the addition of Ni/TCN. Moreover, the MgH2-Ni/TCN sample shows excellent cycle stability, with a dehydrogenation capacity retention rate of 98.0% after 10 cycles. The carbon material enhances sorption kinetics by dispersing and stabilizating MgH2. Otherwise, the phase transformation between Mg2NiH4 and Mg2NiH0.3 accelerates the re/dehydrogenation reaction of the composite. (C) 2021 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:33186 / 33196
页数:11
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