Constructing organic D-A-π-A-featured sensitizers with a quinoxaline unit for high-efficiency solar cells: the effect of an auxiliary acceptor on the absorption and the energy level alignment.

Four organic D-A-π-A-featured sensitizers (TQ1, TQ2, IQ1, and IQ2) have been studied for high-efficiency dye-sensitized solar cells (DSSCs). We employed an indoline or a triphenylamine unit as the donor, cyanoacetic acid as the acceptor/anchor, and a thiophene moiety as the conjugation bridge. Additionally, an electron-withdrawing quinoxaline unit was incorporated between the donor and the π-conjugation unit. These sensitizers show an additional absorption band covering the broad visible range in solution. The contribution from the incorporated quinoxaline was investigated theoretically by using DFT and time-dependent DFT. The incorporated low-band-gap quinoxaline unit as an auxiliary acceptor has several merits, such as decreasing the band gap, optimizing the energy levels, and realizing a facile structural modification on several positions in the quinoxaline unit. As demonstrated, the observed additional absorption band is favorable to the photon-to-electron conversion because it corresponds to the efficient electron transitions to the LUMO orbital. Electrochemical impedance spectroscopy (EIS) Bode plots reveal that the replacement of a methoxy group with an octyloxy group can increase the injection electron lifetime by a factor of 2.4. IQ2 and TQ2 can perform well without any co-adsorbent, successfully suppress the charge recombination from TiO(2) conduction band to I(3)(-) in the electrolyte, and enhance the electron lifetime, resulting in a decreased dark current and enhanced open circuit voltage (V(oc)) values. By using a liquid electrolyte, DSSCs based on dye IQ2 exhibited a broad incident photon-to-current conversion efficiency (IPCE) action spectrum and high efficiency (η=8.50 %) with a short circuit current density (J(sc)) of 15.65 mA cm(-2), a V(oc) value of 776 mV, a fill factor (FF) of 0.70 under AM 1.5 illumination (100 mW cm(-2)). Moreover, the overall efficiency remained at 97% of the initial value after 1000 h of visible-light soaking.

[1]  Hidetoshi Miura,et al.  High efficiency of dye-sensitized solar cells based on metal-free indoline dyes. , 2004, Journal of the American Chemical Society.

[2]  P. Shih,et al.  Carbazole-Based Ladder-Type Heptacylic Arene with Aliphatic Side Chains Leading to Enhanced Efficiency of Organic Photovoltaics , 2011 .

[3]  Ying Fu,et al.  Improvement of dye-sensitized solar cells: what we know and what we need to know , 2010 .

[4]  Mingfei Xu,et al.  The structure–property relationship of organic dyes in mesoscopic titania solar cells: only one double-bond difference , 2011 .

[5]  S. P. Tiwari,et al.  Dithienopyrrole–quinoxaline/pyridopyrazine donor–acceptor polymers: synthesis and electrochemical, optical, charge-transport, and photovoltaic properties , 2011 .

[6]  Hironori Arakawa,et al.  Effect of additives on the photovoltaic performance of coumarin-dye-sensitized nanocrystalline TiO2 solar cells. , 2004, Langmuir : the ACS journal of surfaces and colloids.

[7]  Anders Hagfeldt,et al.  How the nature of triphenylamine-polyene dyes in dye-sensitized solar cells affects the open-circuit voltage and electron lifetimes. , 2010, Langmuir : the ACS journal of surfaces and colloids.

[8]  Takayuki Kitamura,et al.  Role of electrolytes on charge recombination in dye-sensitized TiO(2) solar cell (1): the case of solar cells using the I(-)/I(3)(-) redox couple. , 2005, The journal of physical chemistry. B.

[9]  M. Fischer,et al.  Metallfreie organische Farbstoffe für farbstoffsensibilisierte Solarzellen – von Struktur‐Eigenschafts‐Beziehungen zu Designregeln , 2009 .

[10]  J. Baek,et al.  Novel quinoxaline-based organic sensitizers for dye-sensitized solar cells. , 2011, Organic Letters.

[11]  Masanori Miyashita,et al.  Substituted carbazole dyes for efficient molecular photovoltaics: long electron lifetime and high open circuit voltage performance , 2009 .

[12]  C. Koval,et al.  Ferrocene as an internal standard for electrochemical measurements , 1980 .

[13]  Jomy Joseph,et al.  Oxidation of Alcohols and vic‐Diols with H2O2 by Using Catalytic Amounts of N‐Methylpyrrolidin‐2‐one Hydrotribromide , 2006 .

[14]  Saji Alex,et al.  Dye sensitization of nanocrystalline TiO2: enhanced efficiency of unsymmetrical versus symmetrical squaraine dyes , 2005 .

[15]  Min Xu,et al.  Conveniently synthesized isophorone dyes for high efficiency dye-sensitized solar cells: tuning photovoltaic performance by structural modification of donor group in donor-pi-acceptor system. , 2009, Chemical communications.

[16]  Chen Li,et al.  Polyphenylene-based materials for organic photovoltaics. , 2010, Chemical reviews.

[17]  A. Becke A New Mixing of Hartree-Fock and Local Density-Functional Theories , 1993 .

[18]  Anders Hagfeldt,et al.  Light-Induced Redox Reactions in Nanocrystalline Systems , 1995 .

[19]  I. F. Perepichka,et al.  Dibenzothiophene-S,S-dioxide-fluorene co-oligomers. Stable, highly-efficient blue emitters with improved electron affinity. , 2005, Chemical communications.

[20]  Hiromu Kobayashi,et al.  Temperature dependence of open-circuit voltage in dye-sensitized solar cells , 2009 .

[21]  Hidetoshi Miura,et al.  High-conversion-efficiency organic dye-sensitized solar cells with a novel indoline dye. , 2008, Chemical communications.

[22]  Eiji Suzuki,et al.  Alkyl-functionalized organic dyes for efficient molecular photovoltaics. , 2006, Journal of the American Chemical Society.

[23]  Joachim Luther,et al.  Modeling and interpretation of electrical impedance spectra of dye solar cells operated under open-circuit conditions , 2002 .

[24]  Prashant V. Kamat,et al.  Controlling Dye (Merocyanine-540) Aggregation on Nanostructured TiO2 Films. An Organized Assembly Approach for Enhancing the Efficiency of Photosensitization , 1999 .

[25]  Vincenzo Barone,et al.  Time-dependent density functional theory for molecules in liquid solutions , 2001 .

[26]  Michael Grätzel,et al.  Effect of a coadsorbent on the performance of dye-sensitized TiO2 solar cells: shielding versus band-edge movement. , 2005, The journal of physical chemistry. B.

[27]  Thomas W. Hamann,et al.  Dye-sensitized solar cell redox shuttles , 2011 .

[28]  Yan Cui,et al.  Thiophene-Functionalized Coumarin Dye for Efficient Dye-Sensitized Solar Cells: Electron Lifetime Improved by Coadsorption of Deoxycholic Acid , 2007 .

[29]  Liyuan Han,et al.  A novel metal-free panchromatic TiO2 sensitizer based on a phenylenevinylene-conjugated unit and an indoline derivative for highly efficient dye-sensitized solar cells. , 2011, Chemical communications.

[30]  Gang Zhou,et al.  Incorporating Benzotriazole Moiety to Construct D–A−π–A Organic Sensitizers for Solar Cells: Significant Enhancement of Open-Circuit Photovoltage with Long Alkyl Group , 2011 .

[31]  Donald G. Truhlar,et al.  Adiabatic connection for kinetics , 2000 .

[32]  Assaf Y Anderson,et al.  Structure/function relationships in dyes for solar energy conversion: a two-atom change in dye structure and the mechanism for its effect on cell voltage. , 2009, Journal of the American Chemical Society.

[33]  Eiji Suzuki,et al.  Interfacial electron-transfer kinetics in metal-free organic dye-sensitized solar cells: combined effects of molecular structure of dyes and electrolytes. , 2008, Journal of the American Chemical Society.

[34]  A. Monkman,et al.  Dipolar stabilization of emissive singlet charge transfer excited states in polyfluorene copolymers. , 2008, The journal of physical chemistry. B.

[35]  Moon-Sung Kang,et al.  Molecular engineering of organic sensitizers containing p-phenylene vinylene unit for dye-sensitized solar cells. , 2008, The Journal of organic chemistry.

[36]  Jing Zhang,et al.  Engineering organic sensitizers for iodine-free dye-sensitized solar cells: red-shifted current response concomitant with attenuated charge recombination. , 2011, Journal of the American Chemical Society.

[37]  Jun-Ho Yum,et al.  Panchromatic engineering for dye-sensitized solar cells , 2011 .

[38]  Y. Chang,et al.  Triaryl linked donor acceptor dyads for high-performance dye-sensitized solar cells , 2009 .

[39]  M. Fischer,et al.  Metal-free organic dyes for dye-sensitized solar cells: from structure: property relationships to design rules. , 2009, Angewandte Chemie.

[40]  Jingui Qin,et al.  New pyrrole-based organic dyes for dye-sensitized solar cells: convenient syntheses and high efficiency. , 2009, Chemistry.

[41]  Liyuan Han,et al.  Improvement of efficiency of dye-sensitized solar cells based on analysis of equivalent circuit , 2006 .

[42]  Fred Wudl,et al.  Light‐Emitting Polythiophenes , 2005 .

[43]  Chulwoo Kim,et al.  High molar extinction coefficient organic sensitizers for efficient dye-sensitized solar cells. , 2010, Chemistry.

[44]  G. Wegner,et al.  SYNTHESIS OF ALKYL-SUBSTITUTED AND ALKOXY-SUBSTITUTED BENZILS AND OXIDATIVE COUPLING TO TETRAALKOXYPHENANTHRENE-9,10-DIONES , 1994 .

[45]  Yongfang Li,et al.  Novel two‐dimensional donor–acceptor conjugated polymers containing quinoxaline units: Synthesis, characterization, and photovoltaic properties , 2008 .

[46]  Juan Bisquert,et al.  Physical Chemical Principles of Photovoltaic Conversion with Nanoparticulate, Mesoporous Dye-Sensitized Solar Cells , 2004 .

[47]  Xin Li,et al.  Organic D‐A‐π‐A Solar Cell Sensitizers with Improved Stability and Spectral Response , 2011 .

[48]  Peng Wang,et al.  Redox couple related influences of π-conjugation extension in organic dye-sensitized mesoscopic solar cells , 2011 .

[49]  G. Sharma,et al.  New photosensitizer with phenylenebisthiophene central unit and cyanovinylene 4-nitrophenyl terminal units for dye-sensitized solar cells , 2011 .