Generation of terahertz from ZnGeP2 crystal and its application to record the time-resolved photoacoustic spectra of nitromethane

被引:6
|
作者
Rao, K. S. [1 ]
Ganesh, D. [1 ]
Chaudhary, A. K. [1 ]
机构
[1] Univ Hyderabad, ACRHEM, Hyderabad 500046, Andhra Prades, India
来源
关键词
Pulsed THz; UV; PA spectra; Nitromethane; Methanol; DIFFERENCE-FREQUENCY-GENERATION; LOW-LEVEL DETECTION; OPTICAL RECTIFICATION; DOMAIN SPECTROSCOPY; FINGERPRINT SPECTRA; THERMAL-STABILITY; INTERNAL DYNAMICS; LASER LINES; PHOTODISSOCIATION; EMISSION;
D O I
10.1016/j.optlastec.2018.01.009
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
This paper reports the generation of THz radiation through the optical rectification process from type-I cut Zinc germanium phosphate (ZnGeP(2)or ZGP) crystal using optical parametric amplifier pulses (tunable between 1.15-1.6 mu m range, at 60 fs pulse duration and 1 kHz repetition rate) as pump wavelengths at an average power of 50 mW. Also, we have ascertained the conversion efficiency of the generated THz signal, which is of the order of 0.62% at 1.5 THz. Further, the generated radiation is employed for the recording of absorption bands (in terms of PA spectra) of nitromethane and methanol vapor at room temperature using bandpass filters having central frequencies of 0.5 and 1.5 THz. In addition, we have employed the UV-266 nm as an excitation wavelength to record the time domain photoacoustic (PA) spectra of nitromethane (CH3NO2). In case of UV and THz radiations, the excitation mechanisms follow strong electronic (pi* <- n) and weak vibrational-rotational due to ultrafast transition, respectively. In case of UV 266 nm the characteristic PA spectra has been also presented as a function of vapor pressure and data acquisition time with two different PA cells. The current study reveals the effect of the nanoseconds and the ultrafast pulses on some of the common excited acoustic modes (due to similar functional group), which follow two different types of excitation mechanism. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:126 / 134
页数:9
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