Literature DB >> 23023240

Porphyrin-sensitized solar cells.

Lu-Lin Li1, Eric Wei-Guang Diau.   

Abstract

Nature has chosen chlorophylls in plants as antennae to harvest light for the conversion of solar energy in complicated photosynthetic processes. Inspired by natural photosynthesis, scientists utilized artificial chlorophylls - the porphyrins - as efficient centres to harvest light for solar cells sensitized with a porphyrin (PSSC). After the first example appeared in 1993 of a porphyrin of type copper chlorophyll as a photosensitizer for PSSC that achieved a power conversion efficiency of 2.6%, no significant advance of PSSC was reported until 2005; beta-linked zinc porphyrins were then reported to show promising device performances with a benchmark efficiency of 7.1% reported in 2007. Meso-linked zinc porphyrin sensitizers in the first series with a push-pull framework appeared in 2009; the best cell performed comparably to that of a N3-based device, and a benchmark 11% was reported for a porphyrin sensitizer of this type in 2010. With a structural design involving long alkoxyl chains to envelop the porphyrin core to suppress the dye aggregation for a push-pull zinc porphyrin, the PSSC achieved a record 12.3% in 2011 with co-sensitization of an organic dye and a cobalt-based electrolyte. The best PSSC system exhibited a panchromatic feature for light harvesting covering the visible spectral region to 700 nm, giving opportunities to many other porphyrins, such as fused and dimeric porphyrins, with near-infrared absorption spectral features, together with the approach of molecular co-sensitization, to enhance the device performance of PSSC. According to this historical trend for the development of prospective porphyrin sensitizers used in PSSC, we review systematically the progress of porphyrins of varied kinds, and their derivatives, applied in PSSC with a focus on reports during 2007-2012 from the point of view of molecular design correlated with photovoltaic performance.

Entities:  

Year:  2012        PMID: 23023240     DOI: 10.1039/c2cs35257e

Source DB:  PubMed          Journal:  Chem Soc Rev        ISSN: 0306-0012            Impact factor:   54.564


  64 in total

1.  Interaction of YD2 and TiO₂ in dye-sensitized solar cells (DSSCs): a density functional theory study.

Authors:  Fernando Mendizabal; Alfredo Lopéz; Ramiro Arratia-Pérez; Natalia Inostroza; Cristian Linares-Flores
Journal:  J Mol Model       Date:  2015-08-13       Impact factor: 1.810

2.  Watching energy transfer in metalloporphyrin heterodimers using stimulated X-ray Raman spectroscopy.

Authors:  Jason D Biggs; Yu Zhang; Daniel Healion; Shaul Mukamel
Journal:  Proc Natl Acad Sci U S A       Date:  2013-09-09       Impact factor: 11.205

3.  Metal-free organic sensitizers for use in water-splitting dye-sensitized photoelectrochemical cells.

Authors:  John R Swierk; Dalvin D Méndez-Hernández; Nicholas S McCool; Paul Liddell; Yuichi Terazono; Ian Pahk; John J Tomlin; Nolan V Oster; Thomas A Moore; Ana L Moore; Devens Gust; Thomas E Mallouk
Journal:  Proc Natl Acad Sci U S A       Date:  2015-01-12       Impact factor: 11.205

4.  Does the position of the electron-donating nitrogen atom in the ring system influence the efficiency of a dye-sensitized solar cell? A computational study.

Authors:  Abul Kalam Biswas; Sunirmal Barik; Amitava Das; Bishwajit Ganguly
Journal:  J Mol Model       Date:  2016-05-07       Impact factor: 1.810

Review 5.  Neo-Porphyrinoids: New Members of the Porphyrinoid Family.

Authors:  Poornenth Pushpanandan; Mangalampalli Ravikanth
Journal:  Top Curr Chem (Cham)       Date:  2021-05-19

Review 6.  Solar energy conversion using first row d-block metal coordination compound sensitizers and redox mediators.

Authors:  Catherine E Housecroft; Edwin C Constable
Journal:  Chem Sci       Date:  2022-01-05       Impact factor: 9.825

Review 7.  Small Molecules Containing Amphoteric Imidazole Motifs as Sensitizers for Dye-Sensitized Solar Cells: An Overview.

Authors:  Govardhana Babu Bodedla; Xunjin Zhu; Zhi Zhou; Wai-Yeung Wong
Journal:  Top Curr Chem (Cham)       Date:  2022-09-20

8.  Where Is the Electronic Oscillator Strength? Mapping Oscillator Strength across Molecular Absorption Spectra.

Authors:  Lianjun Zheng; Nicholas F Polizzi; Adarsh R Dave; Agostino Migliore; David N Beratan
Journal:  J Phys Chem A       Date:  2016-03-15       Impact factor: 2.781

9.  Iron sensitizer converts light to electrons with 92% yield.

Authors:  Tobias C B Harlang; Yizhu Liu; Olga Gordivska; Lisa A Fredin; Carlito S Ponseca; Ping Huang; Pavel Chábera; Kasper S Kjaer; Helena Mateos; Jens Uhlig; Reiner Lomoth; Reine Wallenberg; Stenbjörn Styring; Petter Persson; Villy Sundström; Kenneth Wärnmark
Journal:  Nat Chem       Date:  2015-10-12       Impact factor: 24.427

10.  Traumatic Brain Injury Imaging in the Second Near-Infrared Window with a Molecular Fluorophore.

Authors:  Xiao-Dong Zhang; Huasen Wang; Alexander L Antaris; Lulin Li; Shuo Diao; Rui Ma; Andy Nguyen; Guosong Hong; Zhuoran Ma; Joy Wang; Shoujun Zhu; Joseph M Castellano; Tony Wyss-Coray; Yongye Liang; Jian Luo; Hongjie Dai
Journal:  Adv Mater       Date:  2016-06-02       Impact factor: 30.849

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