z-logo
Premium
Improved Hydrogen Absorption/Desorption Properties of MgH 2 by Co–Catalyzing of YH 2 and Co@C
Author(s) -
Xu Cheng,
Lin HuaiJun,
Liu Jiangchuan,
Zhang Peng,
Meng Yuying,
Liu Yana,
Zhang Jiguang,
Li Liquan,
Zhu Yunfeng
Publication year - 2019
Publication title -
chemistryselect
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.437
H-Index - 34
ISSN - 2365-6549
DOI - 10.1002/slct.201901475
Subject(s) - desorption , kinetics , dehydrogenation , catalysis , hydrogen , calcination , chemistry , absorption (acoustics) , hydrogen storage , inorganic chemistry , materials science , adsorption , organic chemistry , physics , quantum mechanics , composite material
Hydrogen absorption and desorption kinetics properties of MgH 2 were improved by co‐doping of commercial YH 2 and a synthesized Carbon supported nano‐Co (Co@C) catalyst, which was prepared by calcination of Zeolitic Imidazolate Framework‐67 (ZIF‐67) precursor. YH 2 addition shows great enhancement on the hydrogen absorption kinetics. The ball‐milled MgH 2 ‐YH 2 absorbs 6.5 wt.% of hydrogen within 100 s at 300 °C. The Co@C catalyst greatly enhances the absorption and desorption kinetics, while the absorption kinetics is slightly slower than that of MgH 2 ‐YH 2 at 250 °C and 275 °C. MgH 2 ‐YH 2 ‐Co@C exhibited prominent absorption and desorption kinetics, reaching full hydrogenation within 150 s at 250 °C and releasing 6 wt.% hydrogen within 1700 s at 300 °C. After hydrogenation and dehydrogenation, particle size of YH 3 remains ∼500 nm, and the fine Co@C particles distributed homogeneously in the MgH 2 matrix.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom