Selective excitation of molecular mode in a mixture by femtosecond resonance-enhanced coherent anti-Stokes Raman scattering spectroscopy

被引:6
作者
He Ping [1 ,2 ]
Li Si-Ning [1 ]
Fan Rong-Wei [1 ]
Li Xiao-Hui [1 ]
Xia Yuan-Qin [1 ]
Yu Xin [1 ]
Chen De-Ying [1 ]
机构
[1] Harbin Inst Technol, Natl Key Lab Sci & Technol Tunable Laser, Inst Optoelect, Harbin 150080, Peoples R China
[2] Harbin Univ Commerce, Coll Fdn Sci, Harbin 150028, Peoples R China
基金
中国国家自然科学基金;
关键词
ultrafast spectroscopy; coherent anti-Stokes Raman scattering; vibrational analysis; resonance enhancement; FRACTIONAL REVIVALS; 2-PHOTON ABSORPTION; ELECTRONIC STATES; IODINE VAPOR; WAVE-PACKET; DYNAMICS; CARS; PORPHYRINS;
D O I
10.1088/1674-1056/21/2/027801
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
Femtosecond time-resolved coherent anti-Stokes Raman scattering (CARS) spectroscopy is used to investigate gaseous molecular dynamics. Due to the spectrally broad laser pulses, usually poorly resolved spectra result from this broad spectroscopy. However, it can be demonstrated that by the electronic resonance enhancement optimization control a selective excitation of specific vibrational mode is possible. Using an electronically resonance-enhanced effect, iodine molecule specific CARS spectroscopy can be obtained from a mixture of iodine-air at room temperature and a pressure of 1 atm (corresponding to a saturation iodine vapour as low as about 35 Pa). The dynamics on either the electronically excited state or the ground state of iodine molecules obtained is consistent with previous studies (vacuum, heated and pure iodine) in the femtosecond time resolved CARS spectroscopy, showing that an effective method of suppressing the non-resonant CARS background and other interferences is demonstrated.
引用
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页数:5
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