Literature DB >> 19081916

Rhodanine dyes for dye-sensitized solar cells : spectroscopy, energy levels and photovoltaic performance.

Tannia Marinado1, Daniel P Hagberg, Maria Hedlund, Tomas Edvinsson, Erik M J Johansson, Gerrit Boschloo, Håkan Rensmo, Tore Brinck, Licheng Sun, Anders Hagfeldt.   

Abstract

Three new sensitizers for photoelectrochemical solar cells were synthesized consisting of a triphenylamine donor, a rhodanine-3-acetic acid acceptor and a polyene connection. The conjugation length was systematically increased, which resulted in two effects: first, it led to a red-shift of the optical absorption of the dyes, resulting in an improved spectral overlap with the solar spectrum. Secondly, the oxidation potential decreased systematically. The excited state levels were, however, calculated to be nearly stationary. The experimental trends were in excellent agreement with density functional theory (DFT) computations. The photovoltaic performance of this set of dyes as sensitizers in mesoporous TiO2 solar cells was investigated using electrolytes containing the iodide/triiodide redox couple. The dye with the best absorption characteristics showed the poorest solar cell efficiency, due to losses by recombination of electrons in TiO2 with triiodide. Addition of 4-tert butylpyridine to the electrolyte led to a strongly reduced photocurrent for all dyes due to a reduced electron injection efficiency, caused by a 0.15 V negative shift of the TiO2 conduction band potential.

Entities:  

Year:  2008        PMID: 19081916     DOI: 10.1039/b812154k

Source DB:  PubMed          Journal:  Phys Chem Chem Phys        ISSN: 1463-9076            Impact factor:   3.676


  11 in total

1.  Effects of physical orientation of dye molecules and molecular orbitals on performance of solid-state dye sensitized solar cells.

Authors:  P K D D P Pitigala; M M Henary; A G U Perera
Journal:  Mater Today Proc       Date:  2019-07-10

2.  Cyano or o-nitrophenyl? Which is the optimal electron-withdrawing group for the acrylic acid acceptor of D-π-A sensitizers in DSSCs? A density functional evaluation.

Authors:  Ji Zhang; Yu-He Kan; Hai-Bin Li; Yun Geng; Yong Wu; Yu-Ai Duan; Zhong-Min Su
Journal:  J Mol Model       Date:  2012-12-29       Impact factor: 1.810

Review 3.  Dye-Sensitized Solar Cells: Fundamentals and Current Status.

Authors:  Khushboo Sharma; Vinay Sharma; S S Sharma
Journal:  Nanoscale Res Lett       Date:  2018-11-28       Impact factor: 4.703

4.  Triphenylamine-based indoline derivatives for dye-sensitized solar cells: a density functional theory investigation.

Authors:  Xue-Feng Ren; Guo-Jun Kang; Qiong-Qiong He
Journal:  J Mol Model       Date:  2015-12-11       Impact factor: 1.810

5.  Optical and Photovoltaic Properties of Thieno[3,2-b]thiophene-Based Push-Pull Organic Dyes with Different Anchoring Groups for Dye-Sensitized Solar Cells.

Authors:  Sara S M Fernandes; M Cidália R Castro; Ana Isabel Pereira; Adélio Mendes; Carlos Serpa; João Pina; Licínia L G Justino; Hugh D Burrows; M Manuela M Raposo
Journal:  ACS Omega       Date:  2017-12-29

6.  Revealing the influence of Cyano in Anchoring Groups of Organic Dyes on Adsorption Stability and Photovoltaic Properties for Dye-Sensitized Solar Cells.

Authors:  Wei-Chieh Chen; Santhanamoorthi Nachimuthu; Jyh-Chiang Jiang
Journal:  Sci Rep       Date:  2017-07-10       Impact factor: 4.379

7.  An Experimental and Theoretical Investigation of the Electronic Structures and Photoelectrical Properties of Ethyl Red and Carminic Acid for DSSC Application.

Authors:  Chaofan Sun; Yuanzuo Li; Peng Song; Fengcai Ma
Journal:  Materials (Basel)       Date:  2016-10-01       Impact factor: 3.623

Review 8.  Recent Advances on Nitrofluorene Derivatives: Versatile Electron Acceptors to Create Dyes Absorbing from the Visible to the Near and Far Infrared Region.

Authors:  Guillaume Noirbent; Frédéric Dumur
Journal:  Materials (Basel)       Date:  2018-11-30       Impact factor: 3.623

9.  Photochemical activation of TRPA1 channels in neurons and animals.

Authors:  David Kokel; Chung Yan J Cheung; Robert Mills; Jaeda Coutinho-Budd; Liyi Huang; Vincent Setola; Jared Sprague; Shan Jin; Youngnam N Jin; Xi-Ping Huang; Giancarlo Bruni; Clifford J Woolf; Bryan L Roth; Michael R Hamblin; Mark J Zylka; David J Milan; Randall T Peterson
Journal:  Nat Chem Biol       Date:  2013-02-10       Impact factor: 15.040

10.  Rhodanine-based Knoevenagel reaction and ring-opening polymerization for efficiently constructing multicyclic polymers.

Authors:  Ze Zhang; Xuan Nie; Fei Wang; Guang Chen; Wei-Qiang Huang; Lei Xia; Wen-Jian Zhang; Zong-Yao Hao; Chun-Yan Hong; Long-Hai Wang; Ye-Zi You
Journal:  Nat Commun       Date:  2020-07-21       Impact factor: 14.919

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.