Role of impurities in determining the exciton diffusion length in organic semiconductors

2016 ◽  
Vol 108 (16) ◽  
pp. 163301 ◽  
Author(s):  
Ian J. Curtin ◽  
D. Wayne Blaylock ◽  
Russell J. Holmes
2016 ◽  
Vol 4 (16) ◽  
pp. 3437-3442 ◽  
Author(s):  
S. Matthew Menke ◽  
Russell J. Holmes

Temperature dependent measurements of the exciton diffusion length (LD) are performed for three archetypical small-molecule, organic semiconductors: aluminum tris-(8-hydroxyquinoline) (Alq3), dicyanovinyl-terthiophene (DCV3T), and boron subphthalocyanine chloride (SubPc).


2020 ◽  
Vol 11 (1) ◽  
Author(s):  
Yuliar Firdaus ◽  
Vincent M. Le Corre ◽  
Safakath Karuthedath ◽  
Wenlan Liu ◽  
Anastasia Markina ◽  
...  

Abstract The short exciton diffusion length associated with most classical organic semiconductors used in organic photovoltaics (5-20 nm) imposes severe limits on the maximum size of the donor and acceptor domains within the photoactive layer of the cell. Identifying materials that are able to transport excitons over longer distances can help advancing our understanding and lead to solar cells with higher efficiency. Here, we measure the exciton diffusion length in a wide range of nonfullerene acceptor molecules using two different experimental techniques based on photocurrent and ultrafast spectroscopy measurements. The acceptors exhibit balanced ambipolar charge transport and surprisingly long exciton diffusion lengths in the range of 20 to 47 nm. With the aid of quantum-chemical calculations, we are able to rationalize the exciton dynamics and draw basic chemical design rules, particularly on the importance of the end-group substituent on the crystal packing of nonfullerene acceptors.


2012 ◽  
Vol 108 (13) ◽  
Author(s):  
Oleksandr V. Mikhnenko ◽  
Roald Ruiter ◽  
Paul W. M. Blom ◽  
Maria Antonietta Loi

2014 ◽  
Vol 1 (2) ◽  
pp. 280-285 ◽  
Author(s):  
Jason D. A. Lin ◽  
Oleksandr V. Mikhnenko ◽  
Jingrun Chen ◽  
Zarifi Masri ◽  
Arvydas Ruseckas ◽  
...  

Six techniques are used to measure the exciton diffusion length as a function of systematic chemical modifications.


2010 ◽  
Vol 22 (11) ◽  
pp. 1233-1236 ◽  
Author(s):  
Richard R. Lunt ◽  
Jay B. Benziger ◽  
Stephen R. Forrest

2019 ◽  
Vol 7 (19) ◽  
pp. 5695-5701 ◽  
Author(s):  
Deepesh Rai ◽  
Russell J. Holmes

We develop a methodology to measure the diffusion of dark triplet excitons in organic semiconductor thin films using a phosphorescent sensitizer-based approach that explicitly quantifies quenching efficiency by varying sensitizer concentration.


2020 ◽  
Vol 89 (3) ◽  
pp. 30201 ◽  
Author(s):  
Xi Guan ◽  
Shiyu Wang ◽  
Wenxing Liu ◽  
Dashan Qin ◽  
Dayan Ban

Organic solar cells based on planar copper phthalocyanine (CuPc)/C60 heterojunction have been characterized, in which a 2 nm-thick layer of bathocuproine (BCP) is inserted into the CuPc layer. The thin layer of BCP allows hole current to tunnel it through but blocks the exciton diffusion, thereby altering the steady-state exciton profile in the CuPc zone (zone 1) sandwiched between BCP and C60. The short-circuit current density (JSC) of device is limited by the hole-exciton scattering effect at the BCP/CuPc (zone 1) interface. Based on the variation of JSC with the width of zone 1, the exciton diffusion length of CuPc is deduced to be 12.5–15 nm. The current research provides an easy and helpful method to determine the exciton diffusion lengths of organic electron donors.


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