氢气储存
纳米孔
动力学
气凝胶
材料科学
解吸
脱氢
化学工程
氢化物
氢
吸附
碳纤维
活化能
多孔性
无机化学
金属
纳米技术
化学
催化作用
吸附
物理化学
复合材料
有机化学
冶金
量子力学
复合数
工程类
物理
作者
Adam F. Gross,John J. Vajo,Sky L Van Atta,Gregory L. Olson
摘要
Enhanced kinetics for hydrogen exchange in LiBH4 incorporated within nanoporous carbon scaffolds are described. Dehydrogenation rates up to 50 times faster than those in the bulk material are measured at 300 °C in a nanostructured hydride formed by filling a porous carbon aerogel host with LiBH4. Furthermore, the activation energy for hydrogen desorption, measured using the approach developed by Ozawa, is reduced from 146 kJ/mol for bulk LiBH4 to 103 kJ/mol for nanostructured LiBH4, and the faster kinetics result in desorption temperatures that are reduced by up to 75 °C. In addition, nanostructured hydrides exhibit increased cycling capacity over multiple sorption cycles. This work demonstrates that confinement within a porous scaffold host is a promising approach for enhancing hydrogen uptake and release in reversible light-metal complex hydrides.
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