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CS_2 ~1B_2(~1Σ_u^+)态预离解产物CS的振转布居研究 被引量:1
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作者 郭颖 周晓国 +4 位作者 徐海峰 李奇峰 戴静华 刘世林 马兴孝 《Chinese Journal of Chemical Physics》 SCIE CAS CSCD 北大核心 2003年第6期435-439,共5页
用一束波长为 2 10 .2 7nm的激光将CS2 分子激发至预离解态1B2 (1Σ+ u) ,用另一束激光通过激光诱导荧光 (LIF)方法检测碎片CS ,在 2 5 0 .5~ 2 86 .5nm获得了CS碎片A1Π←X1Σ+ 振转分辨的激发谱 .通过对光谱强度的分析 ,获得了CS碎片... 用一束波长为 2 10 .2 7nm的激光将CS2 分子激发至预离解态1B2 (1Σ+ u) ,用另一束激光通过激光诱导荧光 (LIF)方法检测碎片CS ,在 2 5 0 .5~ 2 86 .5nm获得了CS碎片A1Π←X1Σ+ 振转分辨的激发谱 .通过对光谱强度的分析 ,获得了CS碎片v″ =0~ 8的振动布居和v″=1,4~ 8振动态的转动布居 .结果发现 ,碎片CS的振动布居呈双模结构 ,分别对应于CS2 分子1B2 (1Σ+ u)态的两个解离通道 ,即CS(X1Σ+ ,v″=0~ 9) +S(3 PJ)和CS(X1Σ+ ,v″ =0~ 1)+S(1B2 ) .由此得到两个解离通道的分支比S(3 PJ) :S(1B2 )为 5 .6± 1.2 .与前人 193nm处的研究结果相比 ,2 10 .2 7nm激发更有利于S(3 PJ)通道的生成 .此外 ,实验还发现CS的转动布居不满足热平衡分布 。 展开更多
关键词 CS2 ^1B2(^1∑u^+)态 振转布居 通道分支比 预离解
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He(2^3S1),NE(^3P0,2)与NH3的传能动力学 被引量:1
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作者 王黎明 李学初 +2 位作者 陈宏 沈关林 楼南泉 《物理化学学报》 SCIE CAS CSCD 北大核心 1995年第8期704-709,共6页
在分子束条件下利用化学发光技术研究了亚稳态惰性气体原子He(23S1)和Ne(3P0,2)与NH3碰撞的解离激发反应.He(23S1)与NH3的反应中观察到NH(A-X,c-a,c-b),NH+(B-X)和H*-Balmer发射.对NH(A-X,c-a)的谱图进行了... 在分子束条件下利用化学发光技术研究了亚稳态惰性气体原子He(23S1)和Ne(3P0,2)与NH3碰撞的解离激发反应.He(23S1)与NH3的反应中观察到NH(A-X,c-a,c-b),NH+(B-X)和H*-Balmer发射.对NH(A-X,c-a)的谱图进行了拟合.分析NH(c-b)谱发现NH(c)倾向于生成具有f对称性的转动能级,NH3可能是经由一个NH2中间体分两步解离,这与121.6nm光解NH3时的倾向性正好相反.利用参比反应测得生成NH(A,c)的速度为k=1.0×10-11cm3·s-1.He(23S1)与NH3生成的NH(A,v’=1)的转动激发比v’=0时要高,根据含角动量守恒的相空间理论,其生成过程可能具有较大的解离半碰撞参数.Ne(3P0,2)与NH3反应只有NH(A-X,c-a)发射,NH(A,c)的振转布居可由简单相空间理论三体解离模式解释. 展开更多
关键词 解离激发 振转布居 传能动力学
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化学发光光谱的计算机模拟及应用 被引量:4
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作者 于化忠 王黎明 +2 位作者 陈宏 顾月姝 李学初 《光谱学与光谱分析》 SCIE EI CAS CSCD 北大核心 1995年第3期61-66,共6页
本文报道了模拟计算化学发光光谱的基本原理和程序编写。以双原于分于NO(A2Σ→X2Π)跃迁为例,系统介绍了模拟的过程和相应的理论处理。同时讨论了常用的面积比方法存在的问题以及光谱模拟在微观反应动力学中对于探讨反应机理... 本文报道了模拟计算化学发光光谱的基本原理和程序编写。以双原于分于NO(A2Σ→X2Π)跃迁为例,系统介绍了模拟的过程和相应的理论处理。同时讨论了常用的面积比方法存在的问题以及光谱模拟在微观反应动力学中对于探讨反应机理的应用。 展开更多
关键词 化学发光光谱 计算机模拟 振转布居
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Isotope Effects on Two-Photon Population Transfer Processes of HF and DF
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作者 庞玉慧 王彬彬 +2 位作者 韩永昌 丛书林 牛英煜 《Chinese Journal of Chemical Physics》 SCIE CAS CSCD 2016年第3期297-302,I0001,共7页
The isotope effects of XF (X=H, D) on the population transfer process via two-photon resonance excitation are investigated by solving the time-dependent SchrSdinger equation. The vibrational levels v=0 and 2 of the ... The isotope effects of XF (X=H, D) on the population transfer process via two-photon resonance excitation are investigated by solving the time-dependent SchrSdinger equation. The vibrational levels v=0 and 2 of the ground electronic state are taken to be the initial and target states, respectively, for the two molecular systems. The influences of the field peak amplitude and pulse duration on the population transfer process are discussed in detail. The pulse duration is required to be longer than 860 fs for the DF molecule to achieve a relatively high transfer probability (more than 80%), while the one for the HF molecule is just required to be longer than 460 fs. Moreover, the intermediate level v=1 and the higher level v=3 may play more important roles in the two-photon resonance process for the DF molecule, compared to the roles in the process for the HF molecule. 展开更多
关键词 Population transfer Two-photon resonance transition Isotope effects DF
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Systematical Study on Photodissociation Dynamics of BrCN from 225 nm to 260 nm
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作者 Tonghui Yin Liying Ma +1 位作者 Hong Gao Min Cheng 《Chinese Journal of Chemical Physics》 SCIE EI CAS CSCD 2022年第1期86-94,I0063,共10页
The photodissociation dynamics of Br-C bond cleavage for BrCN in the wavelength region from 225 nm to 260 nm has been studied by our homebuilt time-slice velocity-map imaging setup.The images for both of the ground st... The photodissociation dynamics of Br-C bond cleavage for BrCN in the wavelength region from 225 nm to 260 nm has been studied by our homebuilt time-slice velocity-map imaging setup.The images for both of the ground state Br(^(2)P_(3/2))and spin-orbit excited Br^(*)(^(2)P_(1/2))channels are obtained at several photodissociation wavelengths.From the analysis of the translational energy release spectra,the detailed vibrational and rotational distributions of CN products have been measured for both of the Br and Br^(*) channels.It is found that the internal excitation of the CN products for the Br^(*) channel is colder than that for the Br channel.The most populated vibrational levels of the CN products are v=0 and 1 for the Br and Br^(*) channels,respectively.For the Br channel,the photodissociation dynamics at longer wavelengths are found to be different from those at shorter wavelengths,as revealed by their dramatically different vibrational and rotational excitations of the CN products. 展开更多
关键词 Photodissociation dynamics Cyanogen bromide Ro-vibronic distribution Energy partitioning Velocity-map imaging
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Enhanced Deflection of Light Ray by Atomic Ensemble on Coherent Population Oscillation
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作者 LU Jing ZHOU Lan KUANG Le-Man 《Communications in Theoretical Physics》 SCIE CAS CSCD 2009年第1期139-144,共6页
In recent experiments [e.g., Nature Physics 2 (2006) 332], the enhanced light deflection in an atomic ensemble due to inhomogeneous fields is demonstrated by the electromagneticaJly induced transparency (EIT) base... In recent experiments [e.g., Nature Physics 2 (2006) 332], the enhanced light deflection in an atomic ensemble due to inhomogeneous fields is demonstrated by the electromagneticaJly induced transparency (EIT) based mechanism. In this paper, we explore a different mechanism for the similar phenomenon of the enhanced light deflection. This mechanism is based on the coherent population oscillation, which leads to the hole burning in the absorption spectrum. The medium causing the deflection of probe light is an ensemble of two-level atoms manipulated by a strong controlled field on the two photon resonances. In the large detuning condition, the response of the medium to the pump field and signal field is obtained with steady state approximation. And it is found that after the probe field travels across the medium, the signal ray bends due to the spatial-dependent profile of the control beam. 展开更多
关键词 coherent population oscillation atomic response large detuning
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