Ultrafast and slow charge recombination dynamics of diketopyrrolopyrrole-NiO dye sensitized solar cells

Lei Zhang, Ludovic Favereau, Yoann Farré, Edgar Mijangos, Yann Pellegrin, Errol Blart, Fabrice Odobel, Leif Hammarström

Research output: Contribution to journalArticle

26 Citations (Scopus)

Abstract

In a photophysical study, two diketopyrrolopyrrole (DPP)-based sensitizers functionalized with 4-thiophenecarboxylic acid as an anchoring group and a bromo (DPPBr) or dicyanovinyl (DPPCN2) group, and a dyad consisting of a DPP unit linked to a naphthalenediimide group (DPP-NDI), were investigated both in solution and grafted on mesoporous NiO films. Femtosecond transient absorption measurements indicate that ultrafast hole injection occurred predominantly on a timescale of ∼200 fs, whereas the subsequent charge recombination occurred on a surprisingly wide range of timescales, from tens of ps to tens of μs; this kinetic heterogeneity is much greater than is typically observed for dye-sensitized TiO2 or ZnO. Also, in contrast to what is typically observed for dye-sensitized TiO2, there was no significant dependence on the excitation power of the recombination kinetics, which can be explained by the hole density being comparatively higher near the valence band of NiO before excitation. The additional acceptor group in DPP-NDI provided a rapid electron shift and stabilized charge separation up to the μs timescale. This enabled efficient (∼95%) regeneration of NDI by a CoIII(dtb)3 electrolyte (dtb = 4,4′-di-tert-butyl-2,2′-bipyridine), according to transient absorption measurements. The regeneration of DPPBr and DPPCN2 by CoIII(dtb)3 was instead inefficient, as most recombination for these dyes occurred on the sub-ns timescale. The transient spectroscopy data thus corroborated the trend of the published photovoltaic properties of dye-sensitized solar cells (DSSCs) based on these dyes on mesoporous NiO, and show the potential of a design strategy with a secondary acceptor bound to the dye. The study identifies rapid initial recombination between the dye and NiO as the main obstacle to obtaining high efficiencies in NiO-based DSSCs; these recombination components may be overlooked when studies are conducted using only methods with ns resolution or slower.

Original languageEnglish
Pages (from-to)18515-18527
Number of pages13
JournalPhysical Chemistry Chemical Physics
Volume18
Issue number27
DOIs
Publication statusPublished - 2016

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Coloring Agents
solar cells
dyes
regeneration
Kinetics
Valence bands
Electrolytes
Dye-sensitized solar cells
diketopyrrolopyrrole dye
kinetics
polarization (charge separation)
Spectroscopy
excitation
Acids
Electrons
electrolytes
injection
valence
trends
acids

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry
  • Physics and Astronomy(all)

Cite this

Ultrafast and slow charge recombination dynamics of diketopyrrolopyrrole-NiO dye sensitized solar cells. / Zhang, Lei; Favereau, Ludovic; Farré, Yoann; Mijangos, Edgar; Pellegrin, Yann; Blart, Errol; Odobel, Fabrice; Hammarström, Leif.

In: Physical Chemistry Chemical Physics, Vol. 18, No. 27, 2016, p. 18515-18527.

Research output: Contribution to journalArticle

Zhang, L, Favereau, L, Farré, Y, Mijangos, E, Pellegrin, Y, Blart, E, Odobel, F & Hammarström, L 2016, 'Ultrafast and slow charge recombination dynamics of diketopyrrolopyrrole-NiO dye sensitized solar cells', Physical Chemistry Chemical Physics, vol. 18, no. 27, pp. 18515-18527. https://doi.org/10.1039/c6cp01762b
Zhang, Lei ; Favereau, Ludovic ; Farré, Yoann ; Mijangos, Edgar ; Pellegrin, Yann ; Blart, Errol ; Odobel, Fabrice ; Hammarström, Leif. / Ultrafast and slow charge recombination dynamics of diketopyrrolopyrrole-NiO dye sensitized solar cells. In: Physical Chemistry Chemical Physics. 2016 ; Vol. 18, No. 27. pp. 18515-18527.
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