Enhanced hydrogen desorption/absorption properties of magnesium hydride with CeF3@Gn

Enhanced hydrogen desorption/absorption properties of magnesium hydride with CeF3@Gn
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CeF3@Gn 增强氢化镁的氢解吸/吸收性能

DOI:
10.1016/j.ijhydene.2019.12.111
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发表时间:
2020-02
影响因子:
7.2
通讯作者:
Yan Mi
Yan Mi
中科院分区:
工程技术2区
文献类型:
--
作者:
He Ting;Wang Xinhua;Liu Haizhen;Gao Shichao;Wang Yuanyuan;Li Shouquan;Yan Mi

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为了提高MgH 2的储氢性能,采用湿法球磨-煅烧的方法制备了石墨烯和CeF 3共催化的MgH 2(以下简称MgH 2 +CeF3@Gn)。研究了CeF3@Gn对MgH 2储氢性能的影响。实验结果表明,CeF3@Gn的加入显著降低了MgH 2的放氢/吸氢温度,改善了MgH 2的放氢/吸氢动力学。Mg + CeF3@Gn的开始放氢温度为232 °C,比未掺杂MgH 2的放氢温度低86 °C,放氢容量达到6.77wt%,是理论容量(6.84wt%)的99%。在300 °C和200 °C下,最大氢脱附速率比未经掺杂的球磨MgH 2快79.5和118倍。即使在150 °C的低温下,脱氢样品(Mg + CeF3@Gn)也表现出优异的吸氢动力学,在50 s内可吸5.71wt%的氢,最大吸氢速率达到15.0wt%H2/min,是未掺杂Mg的1765倍。此外,在15次氢解吸/吸收循环后,没有发生储氢容量的显著降低。Mg + CeF3@Gn催化剂表现出优异的吸放氢动力学性能,这是由于MgF 2和CeH 2 - 3原位生成,以及这些副产物的协同催化作用和Gn独特的结构。
In order to improve the hydrogen storage performance of MgH2, graphene and CeF3co-catalyzed MgH2(hereafter denoted as MgH2+CeF3@Gn) were prepared by wet method ball milling and hydriding, which is a simple and time-saving method. The effect of CeF3@Gn on the hydrogen storage behavior of MgH2was investigated. The experimental results showed that co-addition of CeF3@Gn greatly decreased the hydrogen desorption/absorption temperature of MgH2, and remarkably improved the dehydriding/hydriding kinetics of MgH2. The onset hydrogen desorption temperature of Mg + CeF3@Gn is 232 °C,which is 86 °C lower than that of as-milled undoped MgH2, and its hydrogen desorption capacity reaches 6.77 wt%, which is 99% of its theoretical capacity (6.84 wt%). At 300 °C and 200 °C the maximum hydrogen desorption rates are 79.5 and 118 times faster than that of the as-milled undoped MgH2. Even at low temperature of 150 °C, the dedydrided sample (Mg + CeF3@Gn) also showed excellent hydrogen absorption kinetics, it can absorb 5.71 wt% hydrogen within 50 s, and its maximum hydrogen absorption rate reached 15.0 wt% H2/min, which is 1765 times faster than that of the undoped Mg. Moreover, no eminent degradation of hydrogen storage capacity occurred after 15 hydrogen desorption/absorption cycles. Mg + CeF3@Gn showed excellent hydrogen de/absorption kinetics because of the MgF2and CeH2-3that are formed in situ, and the synergic catalytic effect of these by-products and unique structure of Gn.
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