氢气储存
重量分析
材料科学
氢
铂金
富勒烯
氢溢流
吸附
解吸
吸附低温
碳纤维
密度泛函理论
化学物理
Atom(片上系统)
纳米技术
物理化学
计算化学
催化作用
复合材料
化学
金属
合金
冶金
有机化学
复合数
计算机科学
嵌入式系统
作者
Heebin Lee,Dong Gyu Park,Joonho Park,Yong‐Hoon Kim,Jeung Ku Kang
标识
DOI:10.1002/aenm.202300041
摘要
Abstract The search for hydrogen storage materials allowing the storage of hydrogen in its molecular or atomic form at room temperature to meet the multistage targets such as the US Department of Energy (DOE) ultimate gravimetric and volumetric capacities of 6.5 wt% and 50 kg m ‐3 is of global importance. Here, it is reported that an amorphized defective fullerene (C 60‐ x ) offers a promising solution to this challenge. C 60‐ x immobilized with single‐atom platinum has ≈14‐fold higher surface area accessible for CH bonds compared to a crystalline C 60 , and its micro/meso pores give a ≈20‐fold larger volume for fast hydrogen transport. Indeed, hydrogen storage via spillover on C 60‐ x through pressure swing at room temperature is experimentally demonstrated to enable high reversible gravimetric (6.8 wt%) and volumetric (64.9 kg m ‐3 ) capacities, hitherto the highest reversible capacities close to DOE targets at room temperature. Also, the density functional theory calculations show that a key to efficient hydrogen storage is the preservation of a curved sp 2 ‐type local carbon geometry for spillover, which holds H radicals loosely for fast hydrogen migration. Moreover, H‐atom diffusion on the intact region of C 60‐ x is faster than that on the defect region. Furthermore, excellent capacity retention is achieved over repeated hydrogen adsorption/desorption cycles.
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