Enhanced dehydrogenation performance of LiBH4 by confinement in porous NiMnO3 microspheres

被引:15
作者
Xu, Xiaohong [2 ]
Zang, Lei [2 ]
Zhao, Yaran [2 ]
Liu, Yongchang [1 ,2 ]
Wang, Yijing [2 ]
Jiao, Lifang [2 ]
机构
[1] Univ Sci & Technol Beijing, Inst Adv Mat & Technol, Beijing 100083, Peoples R China
[2] Nankai Univ, Coll Chem, Key Lab Adv Energy Mat Chem MOE, Tianjin 300071, Peoples R China
基金
中国国家自然科学基金;
关键词
LiBH4; Nanoconfinement; Synergistic; Destabilization; Porous NiMnO3 nanoparticles; Hydrogen release; HYDROGEN STORAGE PROPERTIES; METAL-ORGANIC FRAMEWORK; CARBON; DESORPTION; NANOCONFINEMENT; RELEASE; CATALYSIS; KINETICS; NI; LIBH4-MG(BH4)(2);
D O I
10.1016/j.ijhydene.2017.08.088
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
The dehydrogenation behavior of LiBH4 has been investigated when confined into porous NiMnO3 microsphere via a wet chemical impregnation method. The confinement of LiBH4 in the pores of NiMnO3 nanoparticles leads to a significant decrease of the onset and the maximum desorption temperatures. The composites begin to release hydrogen at 150 degrees C and the maximum desorption temperature is 300 degrees C, which are much lower compared to the raw LiBH4. Also, the hydrogen release amount is found to be increased. Moreover, the LiBH4@NiMnO3 composites exhibit excellent dehydrogenation kinetics, with 2.8 wt% hydrogen released in 1 h at 300 degrees C. X-ray diffraction and Fourier transform infrared spectroscopy are used to deduce the desorption mechanism of NiMnO3. (C) 2017 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:25824 / 25830
页数:7
相关论文
共 55 条
[1]  
[Anonymous], J MAT CHEM A
[2]   First-principles study of LiBH4 nanoclusters interaction with models of porous carbon and silica scaffolds [J].
Blonski, Piotr ;
Lodziana, Zbigniew .
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2014, 39 (18) :9848-9853
[3]   Preparation of LiBH4@carbon micro-macrocellular foams: tuning hydrogen release through varying microporosity [J].
Brun, Nicolas ;
Janot, Raphael ;
Sanchez, Clement ;
Deleuze, Herve ;
Gervais, Christel ;
Morcrette, Mathieu ;
Backov, Renal .
ENERGY & ENVIRONMENTAL SCIENCE, 2010, 3 (06) :824-830
[4]   Enhanced hydrogen desorption from the Co-catalyzed LiBH4-Mg(BH4)2 eutectic composite [J].
Chen, Juner ;
Zhang, Yao ;
Xiong, Zhitao ;
Wu, Guotao ;
Chu, Hailiang ;
He, Teng ;
Chen, Ping .
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2012, 37 (17) :12425-12431
[5]   Significantly improved dehydrogenation of LiBH4•NH3 assisted by Al2O3 nanoscaffolds [J].
Chen, Xinyi ;
Cai, Wanyu ;
Guo, Yanhui ;
Yu, Xuebin .
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2012, 37 (07) :5817-5824
[6]   Modification of the hydrogen storage properties of Li3N by confinement into mesoporous carbons [J].
Demir-Cakan, Rezan ;
Tang, Wan Si ;
Darwiche, Ali ;
Janot, Raphael .
ENERGY & ENVIRONMENTAL SCIENCE, 2011, 4 (09) :3625-3631
[7]   Hydrogen storage performance of 5LiBH4+Mg2FeH6 composite system [J].
Deng, Shuaishuai ;
Xiao, Xuezhang ;
Han, Leyuan ;
Li, Yun ;
Li, Shouquan ;
Ge, Hongwei ;
Wang, Qidong ;
Chen, Lixin .
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2012, 37 (08) :6733-6740
[8]   Confinement of NaAIH4 in Nanoporous Carbon: Impact on H2 Release, Reversibility, and Thermodynamics [J].
Gao, Jinbao ;
Adelhelm, Philipp ;
Verkuijlen, Margriet H. W. ;
Rongeat, Carine ;
Herrich, Monika ;
van Bentum, P. Jan M. ;
Gutfleisch, Oliver ;
Kentgens, Arno P. M. ;
de Jong, Krijn P. ;
de Jongh, Petra E. .
JOURNAL OF PHYSICAL CHEMISTRY C, 2010, 114 (10) :4675-4682
[9]   Destabilization of LiBH4 by nanoconfinement in PMMA-co-BM polymer matrix for reversible hydrogen storage [J].
Gosalawit-Utke, Rapee ;
Meethom, Sukanya ;
Pistidda, Claudio ;
Milanese, Chiara ;
Laipple, Daniel ;
Saisopa, Thanit ;
Marini, Amedeo ;
Klassen, Thomas ;
Dornheim, Martin .
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2014, 39 (10) :5019-5029
[10]   Enhanced hydrogen storage kinetics of LiBH4 in nanoporous carbon scaffolds [J].
Gross, Adam F. ;
Vajo, John J. ;
Van Atta, Sky L. ;
Olson, Gregory L. .
JOURNAL OF PHYSICAL CHEMISTRY C, 2008, 112 (14) :5651-5657