Recent developments in tetrathiafulvalene and dithiafulvalene based metal-free organic sensitizers for dye-sensitized solar cells: a mini-review
文献信息
Naresh Duvva, Ushasri Chilakamarthi, Lingamallu Giribabu
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.
期刊推荐

New Journal of Chemistry

Journal of Natural Medicines

Current Opinion in Solid State & Materials Science

Drug Discovery Today

Russian Journal of Applied Chemistry

Russian Journal of Organic Chemistry

Organic Process Research & Development

Russian Chemical Bulletin

Russian Journal of General Chemistry

Saudi Pharmaceutical Journal
相关文献
Calculating and assigning rovibrational energy levels of (15N2O)2, (15N14NO)2, 14N2O–15N2O and 15N14NO–15N2O
DOI: 10.1039/C3CP52548A
Copper(ii) binding to flexible triethanolamine-core PAMAM dendrimers: a combined experimental/in silico approach
Maria Francesca Ottaviani, Michela Cangiotti, Alberto Fattori, Concetta Coppola, Erik Laurini, Xiaoxuan Liu, Cheng Liu, Ling Peng
DOI: 10.1039/C3CP54005G
In situ deposition of Ag–Ag2S hybrid nanoparticles onto TiO2 nanotube arrays towards fabrication of photoelectrodes with high visible light photoelectrochemical properties
Wenguang Fan, Simon Jewell, Yiyi She, Michael K. H. Leung
DOI: 10.1039/C3CP54098G
In situ optical studies of methane and simulated biogas oxidation on high temperature solid oxide fuel cell anodes
John D. Kirtley, Daniel A. Steinhurst, Jeffery C. Owrutsky, Michael B. Pomfret, Robert A. Walker
DOI: 10.1039/C3CP53278J
Protein destabilisation in ionic liquids: the role of preferential interactions in denaturation
Angelo Miguel Figueiredo, Joao Sardinha, Geoffrey R. Moore, Eurico J. Cabrita
DOI: 10.1039/C3CP53395F
Synthesis of CdWO4 nanorods and investigation of the photocatalytic activity
Xiaojuan Bai, Jing Xu, Xinguo Ma, Yongfa Zhu
DOI: 10.1039/C3CP53403K
Strain relaxation and order–disorder phase transition in irradiated MgAl2O4
DOI: 10.1039/C3CP53532K
Ionization-induced π → H site-switching in phenol–CH4 complexes studied using IR dip spectroscopy
Mitsuhiko Miyazaki, Akihiro Takeda, Matthias Schmies, Makoto Sakai, Kentaro Misawa, Shun-ichi Ishiuchi, François Michels, Klaus Müller-Dethlefs, Otto Dopfer, Masaaki Fujii
DOI: 10.1039/C3CP53533A
Rational design, characterization and catalytic application of metal clusters functionalized with hydrophilic, chiral ligands: a proof of principle study
Patrick Schreiber, Martin Ludwig, Mark M. Maturi, Olaf Ackermann, Martin Tschurl, Ueli Heiz
DOI: 10.1039/C3CP53626B
Guanine binding to gold nanoparticles through nonbonding interactions
Xi Zhang, Chang Q. Sun, Hajime Hirao
DOI: 10.1039/C3CP52149D
您可能还喜欢
什么是2-氨基戊烷(CAS号:63493-28-7)?
2-氨基戊烷,又名pentan-2-amine,是一种有机化合物,分子式为C5H11NH2。它是一种无色透明液体,有氨味。该化合物在工业和研究中有一定的应用。
反式-4-[4-[[[5-[(3,4-二氟苯基)氨基]-1,3,4-恶二唑-2-基]羰基]氨基]苯基]环己烷乙酸(CAS号:892489-52-0)的物理化学性质是什么?
该化合物为白色固体,分子量为552.31 g/mol。它在水中溶解度较低,在有机溶剂如乙腈、乙酸乙酯中有较好的溶解性。该化合物具有较高的化学稳定性,对酸和碱具有...
如何处理含有Pyrotinib dimaleate(CAS号:1397922-61-0)的废料?
处理含有Pyrotinib dimaleate 的废料时,应遵循当地的法规要求。首先,收集废料并进行分类,确保没有与其他化学品混合。然后,采取适当的物理和化学处...
在合成中是否有4-(5-5-乙基-1,2,4-噁二唑-3-基)苯甲酸乙酯(CAS号:1166756-79-1)的替代品?
在合成过程中,可以考虑使用其他结构类似的化合物作为替代品,例如苯甲酸酯类化合物,如2-乙基-5-甲基噁二唑基苯甲酸乙酯等。这些替代品可能具有相似的化学性质,但在...
如何处理含有1-((叔丁氧基羰基)氨基)环丁烷甲酸甲酯(CAS号:880166-10-9)的废料?
处理含有该化合物的废液时,应先确保其完全反应并转化为无害物质。对于未反应的化合物,建议采用中和处理后进行蒸馏回收,剩余物可使用化学氧化法或焚烧法进行无害化处理。...
2-({[3,5-二(三氟甲基)苯基]磺酰基}氨基)-4-(甲基硫代)丁酸甲酯(CAS号:175202-21-8)的市场或研究趋势如何?
目前该化合物主要应用于药物合成领域,尤其在开发新型抗癌药物方面具有潜在应用。随着制药行业的持续发展,对于高效、低毒的合成中间体需求增加,预计该化合物的研究和应用...
N,N-乙烯双(碘乙酰胺)(CAS号:7250-43-3)的物理化学性质是什么?
N,N-乙烯双(碘乙酰胺)是一种白色或类白色固体,易溶于乙醇、丙酮等有机溶剂,但在水中溶解度较低。该化合物具有较高的反应活性,可以与其他含有活性氢的化合物发生酰...
7-Fluoro-1H-spiro[furo[3,4-c]pyridine-3,4'-piperidine](CAS号:1283090-73-2)通常如何合成?
该化合物可以通过环合反应合成,首先合成吡啶和哌啶的衍生物,然后在合适的条件下进行环合反应得到目标化合物。常用的催化剂包括某些金属盐类,产率一般在70%-90%之...
处理3-乙酰滇乌碱(CAS号:80787-51-5)时应注意哪些实验室安全事项?
在处理3-乙酰滇乌碱时,应穿戴适当的个人防护装备(PPE),如实验服、手套(丁腈手套或PVC手套)、护目镜和口罩。实验应在通风橱中进行,以减少吸入或皮肤接触的风...
如何储存2-溴-5-硝基-4-羧酸(CAS号:1053655-82-5)?
2-溴-5-硝基-4-羧酸应存放在阴凉、干燥、通风良好的地方,远离火源和热源。避免与还原剂、碱性物质接触。储存容器应密封,防止吸湿。



![2-Methyl-2-propanyl [2-(2-oxa-6-azaspiro[3.3]hept-6-yl)ethyl]carbamate structure 2-Methyl-2-propanyl [2-(2-oxa-6-azaspiro[3.3]hept-6-yl)ethyl]carbamate structure](https://cnstatic.chemtradehub.com/structs/141/1415562-38-7-c0a4.webp)
![4-{[4-(Trifluoromethoxy)benzyl]oxy}benzonitrile structure 4-{[4-(Trifluoromethoxy)benzyl]oxy}benzonitrile structure](https://cnstatic.chemtradehub.com/structs/103/1036629-63-6-2172.webp)
![Benzo[b]naphtho[2,1-d]thiophene structure Benzo[b]naphtho[2,1-d]thiophene structure](https://cnstatic.chemtradehub.com/structs/239/239-35-0-ff90.webp)