Wen, YanweiXie, FanLiu, XiaolinLiu, XiaoChen, RongCho, KyeongjaeShan, Bin2018-09-242018-09-242017-04-132017-04-130360-3199http://hdl.handle.net/10735.1/6117Full text access from Treasures at UT Dallas is restricted to current UTD affiliates.Based on first-principles calculations, the H-2 adsorptions onto six types of modified graphene substrates decorated with light metals (Li, Na, K, Be, Mg, Ca) are investigated to shed light on the factors affecting the H-2 binding energies. It is demonstrated that the introduction of defects and dopants into graphene substrates is essential to prevent the metal clustering and achieve dispersed metal atoms desirable for H-2 adsorption. The interaction between H-2 and alkali/alkali-earth metal decorated graphene systems is attributed to the electrostatic effect induced by polarized dipole-dipole interaction. Via introducing defects and hetero-atoms to modify the electronegativity of the local structure, the H-2 adsorption energy can be tuned by choosing the combination of suitable metals and substrates. The calculated H-2 binding strength is positively correlated to the charge transfer from the metal to the substrates and the dipole momentum of metal decorated substrates. Compared the cases with different metals decoration, Mg and Ca are expected to the most promising candidates for multiple H-2 adsorptions.en©2017 Hydrogen Energy Publications LLCMolecular dynamicsCarbon nanotubesHydrogen--StorageAdsorptionOxidesGrapheneAlkaline earth metalsarticleWen, Yanwei, Fan Xie, Xiaolin Liu, Xiao Liu, et al. 2017. "Tunable H₂ binding on alkaline and alkaline earth metals decorated graphene substrates from first-principles calculations." International Journal of Hydrogen Energy 42(15): 10064-10071.4215