How Important is Working with an Ordered Electrode to Improve the Charge Collection Efficiency in Nanostructured Solar Cells?

被引:49
作者
Gonzalez-Vazquez, J. P. [1 ]
Morales-Florez, Victor [2 ]
Anta, Juan A. [1 ]
机构
[1] Univ Pablo Olavide, Area Quim Fis, Seville, Spain
[2] CSIC Univ Sevilla, Inst Ciencia Mat Sevilla, E-41092 Seville, Spain
来源
JOURNAL OF PHYSICAL CHEMISTRY LETTERS | 2012年 / 3卷 / 03期
关键词
GRAIN MORPHOLOGY; LOW-COST; TRANSPORT; DIFFUSION; DYNAMICS; POLYMER; SEMICONDUCTORS; RECOMBINATION; PERFORMANCE; INJECTION;
D O I
10.1021/jz2015988
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The collection efficiency of carriers in solar cells based on nanostructured electrodes is determined for different degrees or morphological one-dimensional order. The transport process is modeled by random walk numerical simulation in a mesoporous electrode that resembles the morphology of nanostructured TiO2 electrodes typically used in dye-sensitized solar cells and related systems. By applying an energy relaxation procedure in the presence of an external potential, a preferential direction is induced in the system. It is found that the partially ordered electrode can almost double the collection efficiency with respect to the disordered electrode. However, this improvement depends strongly on the probability of recombination. For too rapid or too slow recombination, working with partially ordered electrodes will not be beneficial. The computational method utilized here makes it possible to relate the charge collection efficiency with morphology. The collection efficiency is found to reach very rapidly a saturation value, meaning that, in the region of interest, a slight degree of ordering might be sufficient to induce a large improvement in collection efficiency.
引用
收藏
页码:386 / 393
页数:8
相关论文
共 61 条
[1]   Interpretation of diffusion coefficients in nanostructured materials from random walk numerical simulation [J].
Anta, Juan A. ;
Mora-Sero, Ivan ;
Dittrich, Thomas ;
Bisquert, Juan .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2008, 10 (30) :4478-4485
[2]   Combined effect of energetic and spatial disorder on the trap-limited electron diffusion coefficient of metal-oxide nanostructures [J].
Anta, Juan A. ;
Morales-Florez, Victor .
JOURNAL OF PHYSICAL CHEMISTRY C, 2008, 112 (27) :10287-10293
[3]   Dynamics of charge separation and trap-limited electron transport in TiO2 nanostructures [J].
Anta, Juan A. ;
Mora-Sero, Ivan ;
Dittrich, Thomas ;
Bisquert, Juan .
JOURNAL OF PHYSICAL CHEMISTRY C, 2007, 111 (37) :13997-14000
[4]   Random walk numerical simulation for solar cell applications [J].
Anta, Juan A. .
ENERGY & ENVIRONMENTAL SCIENCE, 2009, 2 (04) :387-392
[5]   Multichromophore light harvesting in hybrid solar cells [J].
Bandara, Jayasundera ;
Willinger, Katja ;
Thelakkat, Mukundan .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2011, 13 (28) :12906-12911
[6]  
Benkstein KD, 2003, J PHYS CHEM B, V107, P7759, DOI 10.1021/jp0226811
[7]  
Bisquert J., 2003, PHYS REV LETT, V91
[8]   A review of recent results on electrochemical determination of the density of electronic states of nanostructured metal-oxide semiconductors and organic hole conductors [J].
Bisquert, Juan ;
Fabregat-Santiago, Francisco ;
Mora-Sero, Ivan ;
Garcia-Belmonte, Germa ;
Barea, Eva M. ;
Palomares, Emilio .
INORGANICA CHIMICA ACTA, 2008, 361 (03) :684-698
[9]   Hopping transport of electrons in dye-sensitized solar cells [J].
Bisquert, Juan .
JOURNAL OF PHYSICAL CHEMISTRY C, 2007, 111 (46) :17163-17168
[10]   Simulation of Steady-State Characteristics of Dye-Sensitized Solar Cells and the Interpretation of the Diffusion Length [J].
Bisquert, Juan ;
Mora-Sero, Ivan .
JOURNAL OF PHYSICAL CHEMISTRY LETTERS, 2010, 1 (01) :450-456