氮气
铅(地质)
相图
相(物质)
化学
材料科学
生物
有机化学
古生物学
作者
Sylvain Pitié,Ken Niwa,Gilles Frapper
标识
DOI:10.1021/acs.jpcc.4c05540
摘要
In this study, we employed a variable-composition evolutionary algorithm in conjunction with first-principles calculations to perform a comprehensive structural search for the Pb–N binary system under pressure and determine a hyperfine pressure–composition phase diagram. The findings revealed the existence of 11 new pressure-stabilized structures in the pressure range of 0–100 GPa and at 0 K. Six nitrogen-rich compositions, PbNz (z = 2–4, 6, 8, and 10), and seven thermodynamically stable phases were identified. The most prevalent nitrogen motif observed in the predicted PbNz phases is the N2 dumbbell (z = 2–4, 6, and 8). As z increases, the lowest N–N vibrational frequencies decrease from 2076 cm–1 in Im3̅ Pb(N2)4 to 1302 cm–1 in I4/mcm Pb(N2) at 25 GPa. This finding is related to a decrease in the charge transfer from Pb to N2 dimers. The νN–N frequencies act as a clear signature of the existence of high-pressure PbNz phases containing N2 dumbbells. In addition to N2 dimers, the aromatic pentazolate unit N5– is stabilized in the I4/m Pb(cyclo-N5)2 phase, which becomes thermodynamically stable at 25 GPa. This nitrogen-rich phase can be recoverable to ambient pressure and exhibits a high detonation velocity of 10.2 km/s. Additionally, one- and two-dimensional covalent nitrogen nets are also observed in PbNz (z = 6 and 8). Infinite polymeric chains are found in PbN6 and a two-dimensional nitrogen covalent net is encountered in Cc Pb@2D-N8, which is composed of fused aromatic 18-rings.
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