Role of the Charge Transfer State in Organic Donor-Acceptor Solar Cells

被引:632
作者
Deibel, Carsten [1 ]
Strobel, Thomas [1 ]
Dyakonov, Vladimir [1 ,2 ]
机构
[1] Univ Wurzburg, D-97074 Wurzburg, Germany
[2] Bavarian Ctr Appl Energy Res ZAE Bayern, D-97074 Wurzburg, Germany
关键词
OPEN-CIRCUIT VOLTAGE; PHOTOINDUCED ELECTRON-TRANSFER; INTERNAL QUANTUM EFFICIENCY; EXCITON DISSOCIATION; BULK HETEROJUNCTIONS; CONJUGATED POLYMER; DETAILED BALANCE; POLARON MOTION; BLEND FILMS; RECOMBINATION;
D O I
10.1002/adma.201000376
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Charge transfer complexes are interfacial charge pairs residing at the donor-acceptor heterointerface in organic solar cell. Experimental evidence shows that it is crucial for the photovoltaic performance, as both photocurrent and open circuit voltage directly depend on it. For charge photogeneration, charge transfer complexes represent the intermediate but essential step between exciton dissotiation and charge extraction. Recombination of free charges to the ground state is via the bound charge transfer state before being lost to the ground state. In terms of the open circuit voltage, its maximum achievable value is determined by the energy of the charge transfer state. An important question is whether or not maximum photocurrent and maximum open circuit voltage can be achieved simultaneously. The impact of increasing the CT energy in order to raise the open circuit voltage, but lowering the kinetic excess energy of the CT complexes at the same time on the charge photogeneration will accordingly be discussed. Clearly, the fundamental understanding of the processes involving the charge transfer state is essential for an optimisation of the performance of organic solar cells.
引用
收藏
页码:4097 / 4111
页数:15
相关论文
共 127 条
[1]   From short to long - Optical and electrical transients in photovoltaic bulk heterojunctions of polyfluorene/fullerenes [J].
Andersson, L. Mattias ;
Inganas, Olle .
CHEMICAL PHYSICS, 2009, 357 (1-3) :120-123
[2]   Hot exciton dissociation in a conjugated polymer [J].
Arkhipov, VI ;
Emelianova, EV ;
Bässler, H .
PHYSICAL REVIEW LETTERS, 1999, 82 (06) :1321-1324
[3]   Why is exciton dissociation so efficient at the interface between a conjugated polymer and an electron acceptor? [J].
Arkhipov, VI ;
Heremans, P ;
Bässler, H .
APPLIED PHYSICS LETTERS, 2003, 82 (25) :4605-4607
[4]   Effective transport energy versus the energy of most probable jumps in disordered hopping systems [J].
Arkhipov, VI ;
Emelianova, EV ;
Adriaenssens, GJ .
PHYSICAL REVIEW B, 2001, 64 (12)
[5]  
ARNE C, 2005, J CHEM PHYS, V122
[6]   Contemporary issues in electron transfer research [J].
Barbara, PF ;
Meyer, TJ ;
Ratner, MA .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (31) :13148-13168
[7]   Excitation transport and charge separation in an organic photovoltaic material: Watching excitations diffuse to interfaces [J].
Barbour, Larry W. ;
Pensack, Ryan D. ;
Hegadorn, Maureen ;
Arzhantsev, Sergei ;
Asbury, John B. .
JOURNAL OF PHYSICAL CHEMISTRY C, 2008, 112 (10) :3926-3934
[8]   Intrinsic photoconduction in PPV-type conjugated polymers [J].
Barth, S ;
Bassler, H .
PHYSICAL REVIEW LETTERS, 1997, 79 (22) :4445-4448
[9]   CHARGE TRANSPORT IN DISORDERED ORGANIC PHOTOCONDUCTORS - A MONTE-CARLO SIMULATION STUDY [J].
BASSLER, H .
PHYSICA STATUS SOLIDI B-BASIC RESEARCH, 1993, 175 (01) :15-56
[10]  
BASSLER H, 1995, PURE APPL CHEM, V67, P377, DOI 10.1117/12.200948