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Intermolecular Interactions in Highly Disordered, Confined Dense N2
Author(s) -
Mario Santoro,
Federico A. Gorelli,
Roberto Bini,
Julien Haines
Publication year - 2017
Publication title -
the journal of physical chemistry letters
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 2.563
H-Index - 203
ISSN - 1948-7185
DOI - 10.1021/acs.jpclett.7b00902
Subject(s) - intermolecular force , intramolecular force , raman spectroscopy , chemical physics , zeolite , molecule , diffraction , silicon , polymerization , materials science , crystallography , nitrogen , chemistry , polymer , physics , stereochemistry , catalysis , organic chemistry , optics , metallurgy , composite material
Molecular nitrogen is a benchmark system for condensed matter and, in particular, for looking at universal properties of strongly confined dense systems. We conducted Raman and X-ray diffraction measurements on a dense and disordered form of molecular nitrogen subnanoconfined in a noncatalytic pure SiO 2 zeolite under pressure, up to 50 GPa. In this form, N 2 -N 2 interactions and, consequently, distances are found to be very close to those of bulk N 2 and intramolecular interactions progressively weaken upon increasing pressure. Surprisingly, the filled zeolite is still crystalline at 50 GPa with silicon in tetrahedral coordination by oxygen, which is a record pressure for this type of coordination among all the known forms of silica. We have thus found a rationale for the polymerization of a number molecules occurring in the microchannels of noncatalytic zeolites under pressure, where the pressure threshold is found to be very similar to that observed in bulk samples.

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