Abstract
We report on the synthesis, electrochemical, photophysical, and photovoltaic properties of a series of three organic dyads comprising a perylene monoimide (PMI) dye connected to a naphthalene diimide (NDI) or a fullerene (C60) for application in dye-sensitized solar cells (DSCs) with nanocrystalline NiO electrodes. It was found that the secondary electron acceptor (NDI or C60) in all the three dyads extends the charge separated state lifetime by about five orders of magnitude compared to the respective parent PMI dye. Nanosecond pump-probe experiments of the NiO/dyads in the presence of the electrolyte show that the reduction of triiodide by the secondary electron acceptor is slow in all the dyads, which we ascribe to a weak driving force for this reaction. This reaction is significantly faster with the cobalt electrolyte (tris(4,4′-di-tert-butyl-2,2′-bipyridine) cobalt(ii/iii)), whose driving force is larger; however, its reaction with the reduced dyads is still rather slow. We demonstrate that the larger photovoltage observed with the cobalt electrolyte (VOC = 285 mV) relative to the iodide electrolyte (VOC = 120 mV) is due to a decrease in the dark current for the former owing to slower interfacial electron transfer of the reduced mediator with the injected holes into the NiO electrode. In terms of photovoltaic performances, the most efficient dyad is the system in which the NDI is directly connected to the PMI (η = 0.14% under AM 1.5 with the cobalt electrolyte), but the dyad containing the fullerene acceptor exhibits the highest IPCE and the highest short circuit current density (IPCE = 57%, J SC = 1.88 mA cm-2) with the iodide electrolyte. The latter performances are attributed to the slightly stronger reducing power of C 60 relative to NDI, which favours the reduction of the mediator in the electrolyte.
| Original language | English |
|---|---|
| Pages (from-to) | 2075-2084 |
| Number of pages | 10 |
| Journal | Energy and Environmental Science |
| Volume | 4 |
| Issue number | 6 |
| DOIs | |
| Publication status | Published - Jun 2011 |
Fingerprint
ASJC Scopus subject areas
- Renewable Energy, Sustainability and the Environment
- Environmental Chemistry
- Pollution
- Nuclear Energy and Engineering
Cite this
Synthesis, photophysical and photovoltaic investigations of acceptor-functionalized perylene monoimide dyes for nickel oxide p-type dye-sensitized solar cells. / Le Pleux, Loïc; Smeigh, Amanda L.; Gibson, Elizabeth; Pellegrin, Yann; Blart, Errol; Boschloo, Gerrit; Hagfeldt, Anders; Hammarström, Leif; Odobel, Fabrice.
In: Energy and Environmental Science, Vol. 4, No. 6, 06.2011, p. 2075-2084.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Synthesis, photophysical and photovoltaic investigations of acceptor-functionalized perylene monoimide dyes for nickel oxide p-type dye-sensitized solar cells
AU - Le Pleux, Loïc
AU - Smeigh, Amanda L.
AU - Gibson, Elizabeth
AU - Pellegrin, Yann
AU - Blart, Errol
AU - Boschloo, Gerrit
AU - Hagfeldt, Anders
AU - Hammarström, Leif
AU - Odobel, Fabrice
PY - 2011/6
Y1 - 2011/6
N2 - We report on the synthesis, electrochemical, photophysical, and photovoltaic properties of a series of three organic dyads comprising a perylene monoimide (PMI) dye connected to a naphthalene diimide (NDI) or a fullerene (C60) for application in dye-sensitized solar cells (DSCs) with nanocrystalline NiO electrodes. It was found that the secondary electron acceptor (NDI or C60) in all the three dyads extends the charge separated state lifetime by about five orders of magnitude compared to the respective parent PMI dye. Nanosecond pump-probe experiments of the NiO/dyads in the presence of the electrolyte show that the reduction of triiodide by the secondary electron acceptor is slow in all the dyads, which we ascribe to a weak driving force for this reaction. This reaction is significantly faster with the cobalt electrolyte (tris(4,4′-di-tert-butyl-2,2′-bipyridine) cobalt(ii/iii)), whose driving force is larger; however, its reaction with the reduced dyads is still rather slow. We demonstrate that the larger photovoltage observed with the cobalt electrolyte (VOC = 285 mV) relative to the iodide electrolyte (VOC = 120 mV) is due to a decrease in the dark current for the former owing to slower interfacial electron transfer of the reduced mediator with the injected holes into the NiO electrode. In terms of photovoltaic performances, the most efficient dyad is the system in which the NDI is directly connected to the PMI (η = 0.14% under AM 1.5 with the cobalt electrolyte), but the dyad containing the fullerene acceptor exhibits the highest IPCE and the highest short circuit current density (IPCE = 57%, J SC = 1.88 mA cm-2) with the iodide electrolyte. The latter performances are attributed to the slightly stronger reducing power of C 60 relative to NDI, which favours the reduction of the mediator in the electrolyte.
AB - We report on the synthesis, electrochemical, photophysical, and photovoltaic properties of a series of three organic dyads comprising a perylene monoimide (PMI) dye connected to a naphthalene diimide (NDI) or a fullerene (C60) for application in dye-sensitized solar cells (DSCs) with nanocrystalline NiO electrodes. It was found that the secondary electron acceptor (NDI or C60) in all the three dyads extends the charge separated state lifetime by about five orders of magnitude compared to the respective parent PMI dye. Nanosecond pump-probe experiments of the NiO/dyads in the presence of the electrolyte show that the reduction of triiodide by the secondary electron acceptor is slow in all the dyads, which we ascribe to a weak driving force for this reaction. This reaction is significantly faster with the cobalt electrolyte (tris(4,4′-di-tert-butyl-2,2′-bipyridine) cobalt(ii/iii)), whose driving force is larger; however, its reaction with the reduced dyads is still rather slow. We demonstrate that the larger photovoltage observed with the cobalt electrolyte (VOC = 285 mV) relative to the iodide electrolyte (VOC = 120 mV) is due to a decrease in the dark current for the former owing to slower interfacial electron transfer of the reduced mediator with the injected holes into the NiO electrode. In terms of photovoltaic performances, the most efficient dyad is the system in which the NDI is directly connected to the PMI (η = 0.14% under AM 1.5 with the cobalt electrolyte), but the dyad containing the fullerene acceptor exhibits the highest IPCE and the highest short circuit current density (IPCE = 57%, J SC = 1.88 mA cm-2) with the iodide electrolyte. The latter performances are attributed to the slightly stronger reducing power of C 60 relative to NDI, which favours the reduction of the mediator in the electrolyte.
UR - http://www.scopus.com/inward/record.url?scp=79958070207&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=79958070207&partnerID=8YFLogxK
U2 - 10.1039/c1ee01148k
DO - 10.1039/c1ee01148k
M3 - Article
AN - SCOPUS:79958070207
VL - 4
SP - 2075
EP - 2084
JO - Energy and Environmental Science
JF - Energy and Environmental Science
SN - 1754-5692
IS - 6
ER -