A topological study of chemical bonds under pressure: solid hydrogen as a model case
Author(s) -
Vanessa Riffet,
Vanessa Labet,
Julia ContrerasGarcía
Publication year - 2017
Publication title -
physical chemistry chemical physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.053
H-Index - 239
eISSN - 1463-9084
pISSN - 1463-9076
DOI - 10.1039/c7cp04349j
Subject(s) - polymerization , trimer , hydrogen bond , chemical physics , cluster (spacecraft) , chemistry , chemical bond , polymer science , degree of polymerization , high pressure , dipole , non covalent interactions , computational chemistry , molecule , thermodynamics , physics , polymer , computer science , organic chemistry , dimer , programming language
International audienceIt is now well recognized that a fundamental understanding of the rules that govern chemistry under pressure is still lacking. Hydrogen being the “simplest” element as well as a central core to high pressure physics, we undertake a general study of the changes in the chemical bonding under pressure. We start from a simple trimer unit that has been found in high pressure phases, whose behavior has been found to reveal the basics of hydrogen polymerization under pressure. Making use of bond analysis tools, mainly the NCI (noncovalent interactions) index, we show that polymerization takes place in three steps: dipolar attraction, repulsion and bond formation. The use of a 1D Wigner–Seitz radius allowed us to extend the conclusions to 3D networks and to analyze their degree of polymerization. On the one hand, this approach provides new insight into the polymerization of hydrogen. On the other hand, it shows that complicated molecular solids can be understood from cluster models, where correlated methods can be applied, main differences in solid state arising at the transition points, where breaking/forming of bonds happens at once instead of continuously like in the cluster model
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