Open Access
Facile synthesis of a Ni3S2@C composite using cation exchange resin as an efficient catalyst to improve the kinetic properties of MgH2
Liang Zeng
1
,
Zhi-Qiang Lan
1
,
Baobao Li
1
,
Huiren Liang
1
,
Xiaobin Wen
1
,
Xiantun Huang
2
,
Jun Tan
3
,
Haizhen Liu
1
,
Wenzheng Zhou
1
,
Jianhua Guo
1
Publication type: Journal Article
Publication date: 2022-12-01
scimago Q1
wos Q1
SJR: 3.282
CiteScore: 22.7
Impact factor: 13.8
ISSN: 22139567
Metals and Alloys
Mechanics of Materials
Abstract
• Ni 3 S 2 @C composites were prepared using cheap cation exchange resins and Ni(CH 3 COO) 2 ⋅4H 2 O. • The comprehensive hydrogen storage performance of MgH 2 was significantly improved by the addition of Ni 3 S 2 @C. • The hydrogenation apparent activation energy of MgH 2 -Ni 3 S 2 @C-4 was 39.6 kJ mol −1 . • The multi-phase (Mg/Mg 2 Ni, Mg/MgS, and Mg/C) interface provided more active sites to improve the hydrogen storage performance of MgH 2 . Carbon materials have excellent catalytic effects on the hydrogen storage performance of MgH 2 . Here, carbon-supported Ni 3 S 2 (denoted as Ni 3 S 2 @C) was synthesized by a facile chemical route using ion exchange resin and nickel acetate tetrahydrate as raw materials and then introduced to improve the hydrogen storage properties of MgH 2 . The results indicated the addition of 10 wt.% Ni 3 S 2 @C prepared by macroporous ion exchange resin can effectively improve the hydrogenation/dehydrogenation kinetic properties of MgH 2 . At 100 °C, the dehydrogenated MgH 2 Ni 3 S 2 @C-4 composite could absorb 5.68 wt.% H 2 . Additionally, the rehydrogenated MgH 2 Ni 3 S 2 @C-4 sample could release 6.35 wt.% H 2 at 275 °C. The dehydrogenation/hydrogenation enthalpy changes of MgH 2 Ni 3 S 2 @C-4 were calculated to be 78.5 kJ mol −1 /−74.7 kJ mol −1 , i.e., 11.0 kJ mol −1 /7.3 kJ mol −1 lower than those of MgH 2 . The improvement in the kinetic properties of MgH 2 was ascribed to the multi-phase catalytic action of C, Mg 2 Ni, and MgS, which were formed by the reaction between Ni 3 S 2 contained in the Ni 3 S 2 @C catalyst and Mg during the first hydrogen absorption–desorption process.
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Total citations:
53
Citations from 2024:
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(67.92%)
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GOST
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Zeng L. et al. Facile synthesis of a Ni3S2@C composite using cation exchange resin as an efficient catalyst to improve the kinetic properties of MgH2 // Journal of Magnesium and Alloys. 2022. Vol. 10. No. 12. pp. 3628-3640.
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Zeng L., Lan Z., Li B., Liang H., Wen X., Huang X., Tan J., Liu H., Zhou W., Guo J. Facile synthesis of a Ni3S2@C composite using cation exchange resin as an efficient catalyst to improve the kinetic properties of MgH2 // Journal of Magnesium and Alloys. 2022. Vol. 10. No. 12. pp. 3628-3640.
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RIS
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TY - JOUR
DO - 10.1016/j.jma.2021.03.013
UR - https://doi.org/10.1016/j.jma.2021.03.013
TI - Facile synthesis of a Ni3S2@C composite using cation exchange resin as an efficient catalyst to improve the kinetic properties of MgH2
T2 - Journal of Magnesium and Alloys
AU - Zeng, Liang
AU - Lan, Zhi-Qiang
AU - Li, Baobao
AU - Liang, Huiren
AU - Wen, Xiaobin
AU - Huang, Xiantun
AU - Tan, Jun
AU - Liu, Haizhen
AU - Zhou, Wenzheng
AU - Guo, Jianhua
PY - 2022
DA - 2022/12/01
PB - Elsevier
SP - 3628-3640
IS - 12
VL - 10
SN - 2213-9567
ER -
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@article{2022_Zeng,
author = {Liang Zeng and Zhi-Qiang Lan and Baobao Li and Huiren Liang and Xiaobin Wen and Xiantun Huang and Jun Tan and Haizhen Liu and Wenzheng Zhou and Jianhua Guo},
title = {Facile synthesis of a Ni3S2@C composite using cation exchange resin as an efficient catalyst to improve the kinetic properties of MgH2},
journal = {Journal of Magnesium and Alloys},
year = {2022},
volume = {10},
publisher = {Elsevier},
month = {dec},
url = {https://doi.org/10.1016/j.jma.2021.03.013},
number = {12},
pages = {3628--3640},
doi = {10.1016/j.jma.2021.03.013}
}
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MLA
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Zeng, Liang, et al. “Facile synthesis of a Ni3S2@C composite using cation exchange resin as an efficient catalyst to improve the kinetic properties of MgH2.” Journal of Magnesium and Alloys, vol. 10, no. 12, Dec. 2022, pp. 3628-3640. https://doi.org/10.1016/j.jma.2021.03.013.