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High-pressure stability, transformations, and vibrational dynamics of nitrosonium nitrate from synchrotron infrared and raman spectroscopy

机译:同步加速器红外和拉曼光谱法测定硝酸硝氮的高压稳定性,转变和振动动力学

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The properties of nitrosonium nitrate (NO~+NO_3~-) were investigated following synthesis by laser heating of N_2O and N_2O_4 under high pressures in a diamond anvil cell. Synchrotron infrared absorption spectra of NO~+NO_3~- were measured at pressures up to 32 GPa at room temperature.Raman spectra were obtained at pressures up to 40 Gpa at room temperature and up to 14 GPa at temperatures down to 80 K. For both lattice and intramolecular vibrational modes, a smooth evolution of spectral bands with pressure indicates that NO~+NO_3~- forms a single phase over a broad range above 10 GPa, whereas marked changes, particularly evident in the Raman spectra at low temperature, indicate a phase transition occurs near 5 GPa. NO~+NO_3~- could be recovered at atmospheric pressure and low temperature, persisting to 180 K. The Raman and IR spectroscopic data suggest that the NO~+NO_3~- produced by laser heating of N_2O followed by decompression may differ in structure or orientational order-disorder from that produced by autoionization of N_2O_4.
机译:在金刚石砧室中,在高压下通过激光加热N_2O和N_2O_4进行合成后,研究了硝酸亚硝酸盐(NO〜+ NO_3〜-)的性质。在室温下最高32 GPa的压力下测量NO〜+ NO_3〜-的同步辐射红外吸收光谱。室温下最高40 Gpa的压力下获得的拉曼光谱;在温度低至80 K时最高14 GPa的条件下获得的拉曼光谱。晶格和分子内的振动模式,随着压力谱带的平滑演化,表明NO〜+ NO_3〜-在高于10 GPa的宽范围内形成单相,而明显的变化,特别是在低温下的拉曼光谱中,则表明相变发生在5 GPa附近。 NO〜+ NO_3〜-可以在常压和低温下回收,持续到180K。拉曼光谱和红外光谱数据表明,激光加热N_2O减压后产生的NO〜+ NO_3〜-的结构或结构可能不同。 N_2O_4自电离产生的取向有序无序。

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