Interfacial engineering and configuration design of bilayered photoanode consisting of macroporous tin dioxide/titanium dioxide for high performance dye-sensitized solar cells
- 1. College of Electronic Science and Engineering, Jilin University (China)
- 2. Changchun Institute of Optics, Fine Mechanics and Physics (China)
Description
Highlights: • Hierarchical SnO2/TiO2 porous nanostructure combines fast electron transport, slow charge recombination and high specific surface area. • SnO2@TiO2 hollow sphere synthesized by a facile water bath method exhibits superior light scattering ability. • High efficiency of 7.79% is achieved for double layered photoanode based on macroporous SnO2/TiO2 composite nanomaterials. - Abstract: Two kinds of tin oxide (SnO2)/titanium oxide (TiO2) composite materials have been synthesized and applied as electrodes in dye-sensitized solar cells (DSSCs) with high performance. The porous SnO2/TiO2 material (PSTM) consisting of SnO2 nanosheets cluster and TiO2 nanoparticles (P25) shows a superior dye adsorption ability due to its large specific surface area (151.1 m2 g−1). The PSTM based cell exhibits the slowest electron recombination rate among the cells tested from electrochemical impedance spectra measurements, and obtains final power conversion efficiency (PCE) up to 6.80%. Another novel structure of SnO2@TiO2 hollow sphere (STHS) prepared via a facile water bath process is designed to improve the light utilization efficiency with its excellent light scattering ability. Though the charge recombination resistance of STHS (25.6 Ω) is smaller than that of P25 (30.6 Ω), the PCE of the DSSCs based on the former is 5.82%, showing over 9.2% increment than the latter (5.33%). This can be mainly ascribed to the enhanced light-harvesting ability and charge collection efficiency of the macroporous hollow sphere structure, both of which contribute to a higher short current density and hence for the better photovoltaic performance. Furthermore, we demonstrate a bilayered film of PSTM (charge conduction layer) and STHS (light scattering layer) as photoanode aiming to further improve the efficiency of DSSC by engineered integration of different promising materials. The results indicate that the PSTM+STHS based cell shows an obvious 14.6% increase of PCE (7.79% with a Jsc of 17.49 mA cm−2, Voc of 0.73 V and FF of 0.61) as compared to the single layered PSTM photoelectrode with the same thickness of ∼6.9 μm, providing the specific evidence for taking full advantages of the superior dye adsorption, fast charge collection as well as strong light harvesting simultaneously. Fundamentally, this study not only provides a scheme for the guidance of effective materials surface and interfacial modification, but also highlights the significance of the ideal photoanode configuration for high-efficiency solar cells application
Availability note (English)
Available from http://dx.doi.org/10.1016/j.electacta.2015.07.102Additional details
Identifiers
- DOI
- 10.1016/j.electacta.2015.07.102;
- PII
- S0013-4686(15)30170-5;
Publishing Information
- Journal Title
- Electrochimica Acta
- Journal Volume
- 176
- Journal Page Range
- p. 845-852
- ISSN
- 0013-4686
- CODEN
- ELCAAV
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 47051159
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- ADSORPTION; COMPARATIVE EVALUATIONS; COMPOSITE MATERIALS; EFFICIENCY; ELECTRONS; LIGHT SCATTERING; NANOMATERIALS; NANOPARTICLES; NANOSTRUCTURES; PHOTOVOLTAIC EFFECT; SOLAR CELLS; SPECIFIC SURFACE AREA; TIN OXIDES; TITANIUM OXIDES
- Descriptors DEC
- CHALCOGENIDES; DIRECT ENERGY CONVERTERS; ELEMENTARY PARTICLES; EQUIPMENT; EVALUATION; FERMIONS; LEPTONS; MATERIALS; OXIDES; OXYGEN COMPOUNDS; PARTICLES; PHOTOELECTRIC CELLS; PHOTOELECTRIC EFFECT; PHOTOVOLTAIC CELLS; PHYSICAL PROPERTIES; SCATTERING; SOLAR EQUIPMENT; SORPTION; TIN COMPOUNDS; TITANIUM COMPOUNDS; TRANSITION ELEMENT COMPOUNDS
Optional Information
- Copyright
- Copyright (c) 2015 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.