首页|12.45~14.10 eV光子能量范围内二氟甲烷振动态分辨的阈值光电子能谱研究

12.45~14.10 eV光子能量范围内二氟甲烷振动态分辨的阈值光电子能谱研究

扫码查看
本文利用阈值光电子-光离子符合实验测量与密度泛函理论计算相结合的方法,对二氟甲烷的阈值光电子能谱进行了重新研究.在12.45~14.10 eV光子能量范围内,观测到具有明显振动结构.在M06-2X/cc-pVTZ水平上计算了 CH2F2中性分子及其阳离子电子基态的几何优化构型和振动频率,在此基础上进行Franck-Condon光谱模拟,并进一步通过引入非谐性因子,获得了与实验光谱完美吻合的模拟光谱.基于这些可靠的振动光谱归属,确定了CH2F2的绝热电离能和垂直电离能分别为12.371±0.010 eV和13.281±0.010 eV,同时还得到了 CH2F2+(X2B1)离子四种a1对称性的振动模式频率.
Exploration of Vibrationally Resolved Threshold Photoelectron Spectrum of Difluoromethane within Photon Energy Range of 12.45-14.10 eV
Threshold photoelectron spectrum of CH2F2 in the photon energy range of 12.45-14.10 eV was re-investigated by means of a combination of photo-electron-photoion coincidence experi-ments and density functional theory calculations.A series of vibrational peaks were distinctly observed in this range.Using optimized geometries and vibrational frequencies of the CH2F2 neutral and its cation in ground state at the M06-2X/cc-pVTZ level of theory,Franck-Condon factor simulations were conducted.Taking into account anharmonicity influences,a perfect agreement between the simulated and experimental spectra has been achieved.From the reliable vibrational assign-ments,adiabatic and vertical ionization energies of CH2F2 are derived as 12.371±0.010 eV and 13.281±0.010 eV,respectively.In addition,the experimental frequencies of four vibra-tional modes with a1 symmetry for CH2F2+(X2B1)ions are determined.

Threshold photoelectron spectroscopyFranck-Condon simulationVibrational frequency analysesIonization energyCH2F2

崔雪琪、杨新浪、于同坡、周晓国、刘世林

展开 >

中国科学技术大学化学物理系,合肥微尺度物质科学国家研究中心,合肥 230026

合肥工业大学物理系,合肥 230009

阈值光电子光谱 Franck-Condon拟合 振动频率分析 电离能 二氟甲烷

2024

化学物理学报(英文版)
中国物理学会

化学物理学报(英文版)

CSTPCDEI
影响因子:0.162
ISSN:1674-0068
年,卷(期):2024.37(6)