Photoinduced infrared absorption spectra of CuCl quantum dots in NaCl

2001 ◽  
Vol 15 (28n30) ◽  
pp. 4005-4008
Author(s):  
K. Yamanaka ◽  
K. Edamatsu ◽  
T. Itoh

We have studied infrared transient absorption spectra of CuCl QDs grown inside a NaCl matrix under tunable UV laser excitation on resonance with the confined excitons. In addition to the transient excited-state absorption, there appears induced IR absorption with lifetime much longer than that of the confined exciton. The peak energy remains at ~0.3 eV regardless of the QD size. The optical density is proportional to the square root of the UV laser power. The decay of the induced absorption is logarithmic on time and is accelerated by the irradiation of light below the band gap. We assign this absorption to be originated from the electron-bound defect center called I e center generated in the NaCl side of the interface and discuss it phenomenon in relation with photo-irradiation effects, such as photofatigue, blinking of the luminescence and hole burning.

Author(s):  
Julian Hniopek ◽  
Carolin Müller ◽  
Thomas Bocklitz ◽  
Michael Schmitt ◽  
Benjamin Dietzek ◽  
...  

2015 ◽  
Vol 32 (8) ◽  
pp. 1693
Author(s):  
Hong Liu ◽  
Yulei Bai ◽  
Yun Zhang ◽  
Shuangli Ye ◽  
Weichao Xu ◽  
...  

Transient absorption spectra have been obtained by pulsed radiolysis and flash spectroscopy of neutral and alkaline solutions of benzophenone under anaerobic conditions. These spectra demonstrate the formation of the ketyl radical ion (C 6 H 5 ) 2 Ċ—O - as a primary product resulting from electron attachment to benzophenone. In neutral solution, the rapid neutralization of the ketyl ion produces the neutral radical (C 6 H 5 ) 2 Ċ—OH, and this is shown by a change in the optical absorption spectrum. Neither of the absorption spectra due to these species is observed in acid solutions. These observations show that in neutral and alkaline solution, the hydrated electron reacts directly with the solute, whereas in acid solution it is converted to the hydrogen atom before reacting with the solute.


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