The influence of 1D, meso- and crystal structures on charge transport and recombination in solid-state dye-sensitized solar cells

被引:19
作者
Docampo, Pablo [1 ]
Aruna, Ivaturi [2 ]
Gunning, Robert [1 ]
Diefenbach, Sandra [3 ,4 ]
Kirkpatrick, James [1 ]
Palumbiny, Claudia M. [3 ,4 ]
Sivaram, Varun [1 ]
Geaney, Hugh [5 ]
Schmidt-Mende, Lukas [3 ,4 ,6 ]
Welland, Mark E. [2 ]
Snaith, Henry J. [1 ]
机构
[1] Univ Oxford, Clarendon Lab, Oxford OX1 3PU, England
[2] Univ Cambridge, Dept Engn, Nanosci Ctr, Cambridge CB3 0FF, England
[3] Dept Phys, D-80799 Munich, Germany
[4] Ctr NanoSci, D-80799 Munich, Germany
[5] Univ Limerick, Dept Chem & Environm Sci, MSSI, Limerick, Ireland
[6] Univ Konstanz, Dept Phys, D-78457 Constance, Germany
关键词
HIGH-EFFICIENCY; ELECTRON-TRANSPORT; TRANSIENT PHOTOCURRENT; LIMITED RECOMBINATION; PHOTOVOLTAGE; DIFFUSION; LAYER; PHOTOCARRIERS; NETWORK;
D O I
10.1039/c3ta11855j
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
We have prepared single crystalline SnO2 and ZnO nanowires and polycrystalline TiO2 nanotubes (1D networks) as well as nanoparticle-based films (3D networks) from the same materials to be used as photoanodes for solid-state dye-sensitized solar cells. In general, superior photovoltaic performance can be achieved from devices based on 3-dimensional networks, mostly due to their higher short circuit currents. To further characterize the fabricated devices, the electronic properties of the different networks were measured via the transient photocurrent and photovoltage decay techniques. Nanowire-based devices exhibit extremely high, light independent electron transport rates while recombination dynamics remain unchanged. This indicates, contrary to expectations, a decoupling of transport and recombination dynamics. For typical nanoparticle-based photoanodes, the devices are usually considered electron-limited due to the poor electron transport through nanocrystalline titania networks. In the case of the nanowire-based devices, the system becomes limited by the organic hole transporter used. In the case of polycrystalline TiO2 nanotube-based devices, we observe lower transport rates and higher recombination dynamics than their nanoparticle-based counterparts, suggesting that in order to improve the electron transport properties of solid-state dye-sensitized solar cells, single crystalline structures should be used. These findings should aid future design of photoanodes based on nanowires or porous semiconductors with extended crystallinity to be used in dye-sensitized solar cells.
引用
收藏
页码:12088 / 12095
页数:8
相关论文
共 51 条
[1]   Solid-state dye-sensitized mesoporous TiO2 solar cells with high photon-to-electron conversion efficiencies [J].
Bach, U ;
Lupo, D ;
Comte, P ;
Moser, JE ;
Weissörtel, F ;
Salbeck, J ;
Spreitzer, H ;
Grätzel, M .
NATURE, 1998, 395 (6702) :583-585
[2]   Determination of rate constants for charge transfer and the distribution of semiconductor and electrolyte electronic energy levels in dye-sensitized solar cells by open-circuit photovoltage decay method [J].
Bisquert, J ;
Zaban, A ;
Greenshtein, M ;
Mora-Seró, I .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (41) :13550-13559
[3]   Analysis of the mechanisms of electron recombination in nanoporous TiO2 dye-sensitized solar cells.: Nonequilibrium steady-state statistics and interfacial electron transfer via surface states [J].
Bisquert, J ;
Zaban, A ;
Salvador, P .
JOURNAL OF PHYSICAL CHEMISTRY B, 2002, 106 (34) :8774-8782
[4]   Electron transport in porous nanocrystalline TiO2 photoelectrochemical cells [J].
Cao, F ;
Oskam, G ;
Meyer, GJ ;
Searson, PC .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (42) :17021-17027
[5]   Dye dependent regeneration dynamics in dye sensitized nanocrystalline solar cells:: Evidence for the formation of a ruthenium bipyridyl cation/iodide intermediate [J].
Clifford, John N. ;
Palomares, Emilio ;
Nazeeruddin, Md. K. ;
Gratzel, M. ;
Durrant, James R. .
JOURNAL OF PHYSICAL CHEMISTRY C, 2007, 111 (17) :6561-6567
[6]   Trap-limited electronic transport in assemblies of nanometer-size TiO2 particles [J].
de Jongh, PE ;
Vanmaekelbergh, D .
PHYSICAL REVIEW LETTERS, 1996, 77 (16) :3427-3430
[7]   Deposition of hole-transport materials in solid-state dye-sensitized solar cells by doctor-blading [J].
Ding, I-Kang ;
Melas-Kyriazi, John ;
Cevey-Ha, Ngoc-Le ;
Chittibabu, Kethinni G. ;
Zakeeruddin, Shaik M. ;
Graetzel, Michael ;
McGehee, Michael D. .
ORGANIC ELECTRONICS, 2010, 11 (07) :1217-1222
[8]   Charge Transport Limitations in Self-Assembled TiO2 Photoanodes for Dye-Sensitized Solar Cells [J].
Docampo, Pablo ;
Guldin, Stefan ;
Steiner, Ullrich ;
Snaith, Henry J. .
JOURNAL OF PHYSICAL CHEMISTRY LETTERS, 2013, 4 (05) :698-703
[9]   Unraveling the Function of an MgO Inter layer in Both Electrolyte and Solid-State SnO2 Based Dye-Sensitized Solar Cells [J].
Docampo, Pablo ;
Tiwana, Priti ;
Sakai, Nobuya ;
Miura, Hidetoshi ;
Herz, Laura ;
Murakami, Takurou ;
Snaith, Henry J. .
JOURNAL OF PHYSICAL CHEMISTRY C, 2012, 116 (43) :22840-22846
[10]   Pore Filling of Spiro-OMeTAD in Solid-State Dye-Sensitized Solar Cells Determined Via Optical Reflectometry [J].
Docampo, Pablo ;
Hey, Andrew ;
Guldin, Stefan ;
Gunning, Robert ;
Steiner, Ullrich ;
Snaith, Henry J. .
ADVANCED FUNCTIONAL MATERIALS, 2012, 22 (23) :5010-5019