氢气储存
氢
化学吸附
材料科学
吸附低温
巴(单位)
纳米技术
化学工程
氢氟酸
储能
化学
催化作用
冶金
有机化学
热力学
物理
功率(物理)
气象学
工程类
作者
Shiyuan Liu,Jieyuan Liu,Xiaofang Liu,Jiaxiang Shang,Xu Li,Ronghai Yu,Jianglan Shui
标识
DOI:10.1038/s41565-020-00818-8
摘要
Hydrogen storage materials are the key to hydrogen energy utilization. However, current materials can hardly meet the storage capacity and/or operability requirements of practical applications. Here we report an advancement in hydrogen storage performance and related mechanism based on a hydrofluoric acid incompletely etched MXene, namely, a multilayered Ti2CTx (T is a functional group) stack that shows an unprecedented hydrogen uptake of 8.8 wt% at room temperature and 60 bar H2. Even under completely ambient conditions (25 °C, 1 bar air), Ti2CTx is still able to retain ~4 wt% hydrogen. The hydrogen storage is stable and reversible in the material, and the hydrogen release is controllable by pressure and temperature below 95 °C. The storage mechanism is deduced to be a nanopump-effect-assisted weak chemisorption in the sub-nanoscale interlayer space of the material. Such a storage approach provides a promising strategy for designing practical hydrogen storage materials. An incompletely etched Ti2CTx stack exhibits highly reversible hydrogen storage under near-ambient conditions by nanopump-effect-assisted weak chemisorption.
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