Delaminated MoS2 as a structural and functional modifier for MgH2 - Better hydrogen desorption kinetics through induced worm-like morphologies

被引:9
|
作者
Setijadi, Eki J. [1 ]
Li, Xiaobo [2 ]
Masters, Anthony F. [2 ]
Maschmeyer, Thomas [2 ,3 ]
Aguey-Zinsou, Kondo-Francois [1 ]
机构
[1] Univ New S Wales, Sch Chem Engn, MERLin Grp, Sydney, NSW 2052, Australia
[2] Univ Sydney, Sch Chem, Lab Adv Catalysis Sustainabil, Sydney, NSW 2006, Australia
[3] Univ Sydney, Australian Inst Nanoscale Sci & Technol, Sydney, NSW 2006, Australia
基金
澳大利亚研究理事会;
关键词
Hydrogen storage; Magnesium; Molybdenum disulfide; Nanoparticles; Thermodynamics; Kinetics; STORAGE PROPERTIES; MAGNESIUM HYDRIDE; EVOLUTION-REACTION; NANOPARTICLES; ABSORPTION; SORPTION; NB2O5; MGO;
D O I
10.1016/j.ijhydene.2015.12.161
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
Magnesium hydride (MgH2) nanoparticles have been synthesized in the presence of MoS2 via a simple hydrogenolysis route, involving the decomposition of di-n-butylmagnesium. Remarkably using delaminated MoS2 instead of bulk MoS2 led to the formation of magnesium worm-like structures, which collapsed and recrystallized to some extent upon hydrogen cycling. Hydrogen release from these structures occurred at a relatively low temperature (300 degrees C), and MoS2 was found to effectively improve the hydrogen desorption kinetics of nanosized MgH2. It took less than 150 min to fully release hydrogen from MgH2 catalyzed by delaminated MoS2. In comparison, uncatalysed nanosized MgH2 particles required more than 300 min. Furthermore, MoS2 was found to significantly influence the thermodynamic properties of the Mg/MgH2 reaction, via the destabilization of the Mg-H bond. Compared to ball-milled MgH2, the MoS2 modified materials showed significantly higher hydrogen absorption plateau pressures (similar to 0.15 MPa). This demonstrates that pathways enabling the tuning of the hydrogen storage properties of nanosized MgH2 toward lower temperatures and fast kinetics may exist. Copyright (C) 2016, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:3551 / 3560
页数:10
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