期刊文献+

K_2(~1∧_g)高位态的预解离和碰撞转移

Predissociation and collisional transfer of the high-lying of the K_2(~1∧_g)
下载PDF
导出
摘要 利用光学双共振和激光光谱技术,测量了K_2(~1A_g)态的预解离率和碰撞转移率.脉冲激光将K_2(1~1∑_g^+)基态激发至1~1∑_u^+态,由连续激光激发1~1∑_u^+至激高位~1A_g态.在不同K密度下,记录~1A_g→~1A_u跃迁的时间分辨荧光,光强的对数与衰变时间成线性关系,从直线的斜率得到~1A_g态的有效寿命,由Stern-Volmer方程得到~1A_g态的辐射率与预解离率之和及总的碰撞去布居截面.在不同的K密度下测量时间积分荧光强度I_3[K_2(~1A_g)→K_2(~1A_u)],I_2[K(6S)→K(4P_(3/2))]和I_1[K(4D)→K(4P_(3/2))],光强比I_1/I_3和I_2/I_3与K密度也成线性关系.从直线的斜率和截距并结合从Stern-Volmer方程得到的结果,确定K_3(~1A_g)的预解离率Γ_(P6S)=(1.2±0.4)×10~7s^(-1),Γ_(P4D)=(0.8±0.3)×10~7s^(-1)和碰撞转移截面σss=(1.9±0.6)×10^(-14)cm^2,σ_(4D)=(9.0±3.0)×10^(-15)cm^2. The high-lying ^1∧g state of K2 is excited by using optical-optical double resonance spectroscopy technique. The predissociative rates and collissonal transfer rates of K2(^1∧g) states are experimentally measured. A pulse laser was used to pump K2 from ground state 1^1∑g^+ to the intermediate 1^1∑u^+ state. Then a cw laser was used to excite high-lying ^1∧g state. Predissociative state radiative process was monitored by time-resolved fluorescence from the upper 1As state to lower rovibrational level of the ^1∧u state. From time-resolved fluorescence for the ^1∧g→^1∧u transition at different K densities, the semilog plots were shown. The slopes yielded the effective lifetimes of the ^1∧g state. Based on the Stern-Volmer equation, the sum of the radiative and predissociative rates and the total cross section for deactivation of the K2 (^1∧g) have been determined means of collision with K is (5.6 ±1.1)× 10^-14 cm62. At different K density, the time-integrated intensities of I3[K2(^1∧g)→K2(^1∧u)],I2[K(6S)→K(4P3/2)] and I1[K(4D)→K(4P3/2)] were measured . The rations I1/I3 and I2/I3 versus the K densities can be fitted by the straight lines. By combining the slope and the intercept with the result obtained by the Stern-Volmer equation we obtain predissociative rates, ГP6S=(1.2±0.4)×10^7s^-1 ,ГP4D=(0.8±0.3)×10^7s^-1 and collisional transfer cross sections σ6S=(1.9±0.6)×10^-14cm^2,σ4D=(9.0±3.0)×10^15cm^2.
出处 《原子与分子物理学报》 CAS CSCD 北大核心 2010年第4期685-694,共10页 Journal of Atomic and Molecular Physics
基金 国家自然科学基金(10664003)
关键词 光谱 碰撞转移 预解离 时间分辨荧光 时间积分强度 K2 spectroscopy, collision transfer, predissociation, time-resolved fluorescence, time-integrated intensity, K2
  • 相关文献

参考文献15

  • 1Hang X, Zhao J Z, Xing G Q, etal. The reaction of Cs(8^2P) and Cs(9^2P) with hydrogen molecules[J]. J. Chem. Phys., 1996, 104(4):1338.
  • 2Chang Y P, Hsiao M K, Liu D K, et al. Rotational and vibrational state distributions of Nail in the reactions of Na(4^2S,3^2D, and 6'S) with H2: insertion versus harpoon-type mechanism [ J ]. J. Chem. Phys. , 2008, 128:234309.
  • 3Liu D K, Lin K C. Rotational population distribution of KH(V=0,1,2,and 3) in the reaction of K(5^2P1, 6^2P1 ,7^2P1) with H2: reaction mechanism and prod- uct energy disposal[J].J. Chem. Phys., 1996, 105 (20) : 9121.
  • 4Bililign S, Hattaway B C, Robinson T L, et al. Farwing scattering studies on the reaction Li^* (2P,3P) +H2→LiH(v″=1,2,J″)+H[J]. T. Chem. Phys., 2001, 114(16): 7052.
  • 5Fan L H, ChenJ J, Lin Y Y, etal. Reaction of Rb (5^2D,7^2S) with H2[J]. J. Phys. Chem. A,1999, 103 : 1300.
  • 6姜轶,刘静,王淑英,戴康,沈异凡.Cs(8S-4F)-Ar,H_2的碰撞能量转移[J].原子与分子物理学报,2009,26(1):97-100. 被引量:2
  • 7Bililign S, Hattaway B C, Geum N, et al. Energy transfer in Li^* (3P)- H2 collisions[J]. J. Phys. Chem. A, 2000, 104: 9454.
  • 8L'Hermite J M, Rehmat G, Vetter R. The Cs(7P)+H2→CsH+ H reaction. Ⅱ. Rotationally resolved total cross sections [J]. J. Chem. Phys. , 1991, 95: 3347.
  • 9Cavero V, L'Hermite J M, Rehmat G, et al. Cs (6D3/2)+H2→CsH+H react-ion. IV. Rotationally resolved total cross sections[J]. J. Chem. Phys. , 1999, 110(7): 3428.
  • 10Lin K C, Chang H C. State-selective reaction of excited potassium atom with hydrogen molecule. K+H2KHq-H [J]. J. Chem. Phys., 1989, 90: 6151.

二级参考文献10

  • 1[1]Lou Y L,Lin K C,Liu D K,et al.Collisional deactivation for K in high-lying 2S and 2D states by H2[J].Phys.Rev.A,1992,46(7):3834
  • 2[2]Bililign S,Hattaway B C,Robinson T L,et al.Far-wing scattering studies on the reaction Li*(2p,3p)+H2→LiH(v″=1,2,J″)+H[J].J.Chem.Phys,2001,114(16):7052
  • 3[3]Vadla C,Horvatic V,Niemax K.Radiative transport and collisional transfer of excitation energy in Cs vapors mixed with Ar or He[J].Spectrochim.Acta B:Atom.Spectrosc.,2003,58:1235
  • 4[4]Fan L H,Chen J J,Liu Y Y,et al.Reaction of Rb(52D,72S) with H2[J].J.Phys.Chem.,1999,A103:1300
  • 5[5]Hattaway B C,Bililign S,Uhl L,et al.Energy transfer in Li(4p)+(Ar,H2,CH4) collisions[J].J.Chem.Phys.,2004,120(4):1739
  • 6[7]Kleiber P D,Wong T H,Bililign S.collisional energy transfer in Na(4p-3d)-He,H2 collisions[J].J.Chem.Phys.,1993,98(2):1101
  • 7[8]Caver V,L′Hermite J M,Rahmat G,et al.Cs(6D3/2)+H2→CsH+H reaction.Ⅳ.Rotationally resolved total cress section[J].J.Chem.Phys.,1999,110(7):3428
  • 8[9]L′Hermite J M,Rahmat G,Vetter R.The Cs(7P)+H2→CsH+H reaction Ⅱ.Rotationally resovlved total cross sections[J].J.Chem.Phys.,1991,95(5):3347
  • 9[10]Visticot J P,Ferray M,Cozingot J,et al.Investigation of various ways of forming CsH by irradiating a Cs+H2 mixture with laser light[J].J.Chem.Phys.,1983,79 (6):2839
  • 10[11]Theodosiou C E.Lifetimes of alkali-metal-atom Rydberg states[J].Phys.Rev.A,1984,30(6):2881

共引文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部