scholarly journals The use of near-infrared charge-transfer transitions of low-spin ferric chlorins in axial ligand assignment

FEBS Letters ◽  
1994 ◽  
Vol 356 (2-3) ◽  
pp. 159-161 ◽  
Author(s):  
Qinyun Peng ◽  
Jim Peterson
2018 ◽  
Vol 9 (6) ◽  
pp. 1610-1620 ◽  
Author(s):  
Ryan M. Clarke ◽  
Tiffany Jeen ◽  
Serena Rigo ◽  
John R. Thompson ◽  
Loren G. Kaake ◽  
...  

We detail the rational design of a series of bimetallic bis-ligand radical Ni salen complexes in which the relative orientation of the ligand radical chromophores provides a mechanism to tune the energy of intense intervalence charge transfer (IVCT) bands in the near infrared (NIR) region.


2019 ◽  
Vol 21 (30) ◽  
pp. 16665-16675 ◽  
Author(s):  
Iván González-Veloso ◽  
Jesús Rodríguez-Otero ◽  
Enrique M. Cabaleiro-Lago

The endohedral alkali cations in M+@C60⋯[10]CPP complexes boost the near infrared absorption bands associated with charge transfer from the nanoring to the fullerene.


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Jonas Kublitski ◽  
Axel Fischer ◽  
Shen Xing ◽  
Lukasz Baisinger ◽  
Eva Bittrich ◽  
...  

AbstractDetection of electromagnetic signals for applications such as health, product quality monitoring or astronomy requires highly responsive and wavelength selective devices. Photomultiplication-type organic photodetectors have been shown to achieve high quantum efficiencies mainly in the visible range. Much less research has been focused on realizing near-infrared narrowband devices. Here, we demonstrate fully vacuum-processed narrow- and broadband photomultiplication-type organic photodetectors. Devices are based on enhanced hole injection leading to a maximum external quantum efficiency of almost 2000% at −10 V for the broadband device. The photomultiplicative effect is also observed in the charge-transfer state absorption region. By making use of an optical cavity device architecture, we enhance the charge-transfer response and demonstrate a wavelength tunable narrowband photomultiplication-type organic photodetector with external quantum efficiencies superior to those of pin-devices. The presented concept can further improve the performance of photodetectors based on the absorption of charge-transfer states, which were so far limited by the low external quantum efficiency provided by these devices.


2015 ◽  
Vol 14 (01) ◽  
pp. 1550002 ◽  
Author(s):  
Kaushik Hatua ◽  
Prasanta K. Nandi

Multimetallocene complexes ( Cp – M n– Cp ) of Be , Mg and Ca have been considered for the theoretical study of static second hyperpolarizability using a number of DFT functionals. Owing to the cooperative effect in bonding, beryllium forms multiberyllocene complexes ( Cp – Be n– Cp ) which have sufficient thermal stability with respect to dissociation into neutral fragments up to n = 10. On the other hand, multimetallocene complexes of Mg and Ca are found to be stable for n ≤ 5 which may be due to the weaker covalent bonding interaction between the larger metal atoms. The rather small variation of linear and cubic polarizabilities of Cp – Be n– Cp complexes beyond n = 5 arises from the rather weaker charge transfer transitions. The difference in NLO property among the investigated metal complexes arises from the extent of charge transfer from the terminal metal atoms and the distance between them. The charge transfer at longer distances in the ground state of Mg and Ca complexes leads to more intense electronic transition — the spectroscopic parameters of which strongly favors the enhancement of second hyperpolarizability.


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