Transition from chemisorption to physisorption of H2 on Ti functionalized [2,2,2]paracyclophane: A computational search for hydrogen storage
نویسندگان
چکیده
In this work, we studied the hydrogen adsorption-desorption properties and storage capacities of Ti functionalized [2,2,2]paracyclophane (PCP222) using density functional theory molecular dynamic simulation. The atom was bonded strongly with benzene ring PCP222 via Dewar interaction. Subsequently, calculation diffusion energy barrier revealed a significantly high 5.97 eV preventing clustering over surface. On adsorption hydrogen, first H2 molecule chemisorbed binding 1.79 metals. Further addition molecules, however, exhibited their PCP222-Ti through Kubas-type Charge transfer mechanism during explored by Hirshfeld charge analysis electrostatic potential map, PDOS, Bader's topological nature interaction between H2. three atoms showed maximum uptake capacity up to 7.37 wt%, which fairly above US-DOE criterion. practical estimation that at ambient conditions, gravimetric 6.06 wt% molecules could be usable, 1.31 adsorbed were retained host. ADMP dynamics simulations assured reversibility desorption structural integrity host material sufficiently temperature (300 K 500 K). Therefore, Ti-functionalized can considered as thermodynamically viable potentially reversible material.
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Department of Chemistry & Key Laboratory of Organic Optoelectronics and Molecular Engineering of Ministry of Education, Tsinghua UniVersity, Beijing 100084, China, Department of Physics, Washington State UniVersity, 2710 UniVersity DriVe, Richland, Washington 99354, and Chemical & Materials Sciences DiVision, Pacific Northwest National Laboratory, MS K8-88, P.O. Box 999, Richland, Washington 99352
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ژورنال
عنوان ژورنال: Journal of energy storage
سال: 2023
ISSN: ['2352-1538', '2352-152X']
DOI: https://doi.org/10.1016/j.est.2023.106951