Recent developments in tetrathiafulvalene and dithiafulvalene based metal-free organic sensitizers for dye-sensitized solar cells: a mini-review

Literature Information

Publication Date 2017-04-13
DOI 10.1039/C7SE00068E
Impact Factor 6.367
Authors

Naresh Duvva, Ushasri Chilakamarthi, Lingamallu Giribabu


View Original

Abstract

Currently, there is a great need for green and clean energy sources to meet the needs of the ever-increasing population in the world. Consequently, scientists across the globe are paying much attention to the development of low cost and high performance renewable energy devices. Dye-sensitized solar cells (DSSCs) are the front-runners among new solar cell technologies owing to their low production cost and high efficiency. Dyes (sensitizers) are one of the essential components of DSSC devices in which the widely used sensitizers are Ru(II) polypyridyl complexes. Despite the fact that Ru(II) polypyridyl complexes show high efficiency, they have limitations due to technical constrains. Hence, research has been accelerated in the design and synthesis of various dyes based on non-ruthenium metal complexes, porphyrins, phthalocyanines and metal-free organic compounds. In recent years, tetrathiafulvalenes (TTFs), dithiafulvalenes (DTFs) and their derivatives have been found to be best alternatives to Ru(II) polypyridyl complexes based on their easy synthesis, and electronic and thermal properties. In this review, we summarize the recent progress in metal-free organic dyes using TTF and DTF scaffolds for dye-sensitized solar cells. The physical properties of devices can be tuned via the strategic design of sensitizers, which in turn help in increasing the performance of the devices. Herein, special attention is paid to correlate the structure activity relationship of the components of D–π–A systems to gain insight into the efficient design strategies.

Related Literature

Revolutionizing the structural design and determination of covalent–organic frameworks: principles, methods, and techniques

Yikuan Liu, Xiaona Liu, An Su, Chengtao Gong, Shenwei Chen, Liwei Xia, Chengwei Zhang, Xiaohuan Tao, Yue Li, Yonghe Li, Tulai Sun, Mengru Bu, Wei Shao, Jia Zhao, Xiaonian Li, Yongwu Peng, Yihan Zhu

2023-12-15 Review Article

DOI: 10.1039/D3CS00287J

Strengths of covalent bonds in LnO2 determined from O K-edge XANES spectra using a Hubbard model

Wayne W. Lukens, Jr, Stefan G. Minasian, Corwin H. Booth

2023-11-03 Edge Article

DOI: 10.1039/D3SC03304J

Strategies to engineer various nanocarrier-based hybrid catalysts for enhanced chemodynamic cancer therapy

Ji-Na Hao, Kaiming Ge, Guoli Chen, Bin Dai

2023-10-24 Tutorial Review

DOI: 10.1039/D3CS00356F

Nanotechnologies in ceramic electrochemical cells

Jiafeng Cao, Yuexia Ji, Zongping Shao

2023-12-15 Review Article

DOI: 10.1039/D3CS00303E

Trialkylphosphonium oxoborates as C(sp3)–H oxyanion holes and their application in catalytic chemoselective acetalization

Vincent Ming-Yau Leung, Hong-Chai Fabio Wong, Chun-Man Pook, Ying-Lung Steve Tse, Ying-Yeung Yeung

2023-10-20 Edge Article

DOI: 10.1039/D3SC03081D

Contents list

2024-01-22 Front/Back Matter

DOI: 10.1039/D4CS90006E

Azaphosphinines and their derivatives

J. Nolan McNeill, Jeremy P. Bard, Darren W. Johnson, Michael M. Haley

2023-11-24 Review Article

DOI: 10.1039/D3CS00737E

The synthesis and application of crystalline–amorphous hybrid materials

Hao Lan, Jiawei Wang, Liwei Cheng, Dandan Yu, Hua Wang, Lin Guo

2023-12-20 Review Article

DOI: 10.1039/D3CS00860F

Photoinduced asymmetric charge trapping in a symmetric tetraazapyrene-fused bis(tetrathiafulvalene) conjugate

Ping Zhou, Maryam Nazari Haghighi Pashaki, Hans-Martin Frey, Andreas Hauser, Silvio Decurtins, Andrea Cannizzo, Thomas Feurer, Robert Häner, Shi-Xia Liu

2023-10-25 Edge Article

DOI: 10.1039/D3SC03184E

You might also like

Compound Q&A

What are the main uses of (3alpha,5alpha)-3-Hydroxypregnane-11,20-dione (CAS: 23930-19-0)?

(3alpha,5alpha)-3-Hydroxypregnane-11,20-dione is primarily used in the pharmaceu...

23930-19-0(3alpha,5alpha)-3-Hy...
Compound Q&A

What is the market or research trend for 4-Amino-6-chloro-2-pyridinecarboxylic acid (CAS: 546141-56-4)?

The market for 4-Amino-6-chloro-2-pyridinecarboxylic acid (CAS: 546141-56-4) is ...

546141-56-44-Amino-6-chloro-2-p...
Compound Q&A

Are there alternatives to (2-Benzoylethyl)trimethylammonium chloride (CAS: 24472-88-6) in synthesis?

Alternatives to (2-Benzoylethyl)trimethylammonium chloride (CAS: 24472-88-6) in ...

24472-88-6(2-Benzoylethyl)trim...
Compound Q&A

Is N-[4-Nitro-3-(trifluoromethyl)phenyl]acetamide (CAS: 393-12-4) safe?

N-[4-Nitro-3-(trifluoromethyl)phenyl]acetamide (CAS: 393-12-4) is generally safe...

393-12-4N-[4-Nitro-3-(triflu...
Compound Q&A

Are there alternatives to N,N'-Bis(3-aminopropyl)-1,3-propanediamine (CAS: 4605-14-5) in synthesis?

There are alternatives to N,N'-Bis(3-aminopropyl)-1,3-propanediamine (CAS: 4605-...

4605-14-5N,N'-Bis(3-aminoprop...
Compound Q&A

What precautions should be taken when handling Aluminium trihexadecanoate (CAS: 555-35-1)?

When handling Aluminium trihexadecanoate, it is important to use appropriate per...

555-35-1Aluminium trihexadec...
Compound Q&A

What is (1,1-Dioxido-3-oxo-1,2-benzothiazol-2(3H)-yl)acetic acid (CAS: 52188-11-1)?

(1,1-Dioxido-3-oxo-1,2-benzothiazol-2(3H)-yl)acetic acid is a chemical compound ...

52188-11-1(1,1-Dioxido-3-oxo-1...
Compound Q&A

Are there alternatives to 5,5-dimethyloxolan-2-one (CAS: 3123-97-5) in synthesis?

Several alternatives to 5,5-dimethyloxolan-2-one (CAS: 3123-97-5) can be used in...

3123-97-55,5-dimethyloxolan-2...
Disclaimer
This page provides academic journal information for reference and research purposes only. We are not affiliated with any journal publishers and do not handle publication submissions. For publication-related inquiries, please contact the respective journal publishers directly.
If you notice any inaccuracies in the information displayed, please contact us at support@chemtradehub.com. We will promptly review and address your concerns.