Published October 1, 2012 | Version v1
Journal article

Low temperature synthesis of flower-like TiO2 nanospheres directly from block-graft copolymer precursors and their uses in quasi-solid-state dye-sensitized solar cells

  • 1. Department of Chemical and Biomolecular Engineering, Yonsei University, 262 Seongsanno, Seodaemun-gu, Seoul 120-749 (Korea, Republic of)
  • 2. Department of Environmental Engineering and Energy, Myongji University, Yongin, Kyeonggido 499-728 (Korea, Republic of)

Description

We report a low temperature synthetic method for preparing flower-like TiO2 nanospheres (f-TiO2 NS) directly from an amphiphilic block-graft copolymer precursor. The copolymer, consisting of poly(ethylene glycol) titanium triisopropoxide (PEGTTIP) and polystyrene (PS), was synthesized via atom transfer radical polymerization (ATRP) and was characterized by Fourier transform infrared (FT-IR) spectroscopy. The copolymer was directly hydrolyzed at 90 °C for 6 h without any additives to generate rutile-phase f-TiO2 NS that were approximately 800 nm in size, as confirmed by field emission scanning electron microscopy (FE-SEM), energy-filtering transmission electron microscopy (EF-TEM) and X-ray diffraction (XRD). The energy conversion efficiency of quasi-solid-state dye-sensitized solar cells (qssDSSCs) fabricated with f-TiO2 NS (4.4% at 100 mW/cm2) as a scattering layer (SL) was greater than those without f-TiO2 NS (3.8% for 10 μm, 3.9% for 17 μm) and was quite comparable to cells with a commercial scattering layer (CSL). The improved efficiency is attributed to the increased dye loading and improved light scattering effect, as confirmed by incident photon-to-electron conversion efficiency (IPCE) measurements

Availability note (English)

Available from http://dx.doi.org/10.1016/j.electacta.2012.06.058

Additional details

Identifiers

DOI
10.1016/j.electacta.2012.06.058;
PII
S0013-4686(12)01033-X;

Publishing Information

Journal Title
Electrochimica Acta
Journal Volume
80
Journal Page Range
p. 27-33
ISSN
0013-4686
CODEN
ELCAAV

Optional Information

Copyright
Copyright (c) 2012 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.