氢气储存
氢
化学吸附
材料科学
吸附低温
堆栈(抽象数据类型)
巴(单位)
纳米技术
化学工程
氢氟酸
储能
化学
催化作用
计算机科学
冶金
有机化学
热力学
物理
功率(物理)
气象学
工程类
程序设计语言
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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