PbS/CH3NH3PbI3 Sensitized Quantum dot solar cells Based on efficient charge extracting Nanorods
Gabseok Seo a, Tae Kyu Ahn a
a Sungkyunkwan Univ, KRICT, 83205, Research complex 2 , Sungkyunkwan University, Suwon, gyunggi-do, S.korea, 440746, Korea, Republic of
International Conference on Hybrid and Organic Photovoltaics
Proceedings of International Conference on Hybrid and Organic Photovoltaics 2015 (HOPV15)
Roma, Italy, 2015 May 11th - 13th
Organizer: Filippo De Angelis
Poster, Gabseok Seo, 314
Publication date: 5th February 2015
Semiconductor quantum dots (QDs) have received great attention as a solar energy material due to a high extinction coefficient, tunable band gap, easy production, large dipole moment and multiple exciton generation (MEG) effect. Among them, PbS is one of most explored materials in QD solar cells because of a broad light harvesting from the visible to the infrared (IR) range by easily adjusting QD sizes. Recently, it was reported that lead halide perovskite materials (CH3NH3PbX3, X=Cl, Br, I) possess a high carrier mobility and long carrier diffusion length. Herein, we report fast charge extracting template TiO2 nanorod (NRs) electrode with directly attached PbS QDs/CH3NH3PbI3 Core/Shell-sensitizer. The  successive ionic layer adsorption and reaction (SILAR) application of a PbI2 and Na2S solution on mesoporous TiO2 electrode by repeating spin-coating and the subsequent dipping into CH3NH3I solution in a final stage enabled the formation of CH3NH3PbI3-capped PbS QDs. Then, hole transporting polymers (P3HT and PEDOT:PSS) were also spin-coated and an Au counter electrode was deposited by thermal evaporation to complete the device. The resulting device showed a fully filled with PbS QDs/CH3NH3PbI3 sensitized solar cell reaching overall efficiency to 4.1% under simulated solar illumination (AM1.5, 100 mW·cm-2). (See Figure as below)
Figure 1 Solar cell performance of PbS quantum dots and enclosed in situ with Perovskite thin layer
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