scholarly journals An Effective D-π-A Type Donor Material Based on 4-Fluorobenzoylacetonitrile Core Unit for Bulk Heterojunction Organic Solar Cells

2021 ◽  
Vol 11 (2) ◽  
pp. 646
Author(s):  
Shabaz Alam ◽  
M. Shaheer Akhtar ◽  
Abdullah ◽  
Eun-Bi Kim ◽  
Hyung-Shik Shin ◽  
...  
Keyword(s):  
Solar Cells ◽  
Molecular Orbital ◽  
Organic Solar Cells ◽  
High Performance ◽  
Bulk Heterojunction ◽  
Energy Levels ◽  
Photovoltaic Properties ◽  
Donor Material ◽  
Highest Occupied Molecular Orbital ◽  
Lowest Unoccupied Molecular Orbital

In order to develop new and effective donor materials, a planar donor-π-acceptor (D-π-A) type small organic molecule (SOM), 2-(4-fluorobenzoyl)-3-(5″-hexyl-[2,2′:5′,2″-terthiophen]-5-yl) acrylonitrile, named as H3T-4-FOP, was synthesized by the reaction of 4-fluorobenzoylacetonitrile (as acceptor unit) and hexyl terthiophene (as donor unit) derivatives. Promising optical, solubility, electronic and photovoltaic properties were observed for the H3T-4-FOP SOM. Significantly, the presence of 4-fluorobenzoylacetonitrile as an acceptor unit in H3T-4-FOP SOM tuned the optical band gap to ~2.01 eV and procured the reasonable energy levels as highest occupied molecular orbital (HOMO) of −5.27 eV and lowest unoccupied molecular orbital (LUMO) −3.26 eV. The synthesized H3T-4-FOP SOM was applied as a donor material to fabricate solution-processed bulk heterojunction organic solar cells (BHJ-OSCs) with an active layer of H3T-4-FOP: PC61BM (1:2, w/w) and was validated as having a good power conversion efficiency (PCE) of ~4.38%. Our studies clearly inspire for future designing of multifunctional groups containing the 4-fluorobenzoylacetonitrile based SOM for high performance BHJ-OSCs.

scholarly journals Emphasizing the Operational Role of a Novel Graphene-Based Ink into High Performance Ternary Organic Solar Cells

2019 ◽  
Author(s):  
Minas M. Stylianakis ◽  
Dimitriοs M. Kosmidis ◽  
Katerina Anagnostou ◽  
Christos Polyzoidis ◽  
Miron Krassas ◽  
...  
Keyword(s):  
Solar Cells ◽  
Molecular Orbital ◽  
Organic Solar Cells ◽  
High Performance ◽  
Energy Levels ◽  
Fullerene Derivative ◽  
Highest Occupied Molecular Orbital ◽  
Lowest Unoccupied Molecular Orbital ◽  
Synthetic Routes

A novel solution-processed graphene-based material was synthesized by treating graphene oxide (GO) with 2,5,7-trinitro-9-oxo-fluorenone-4-carboxylic acid (TNF-COOH) moieties, via simple synthetic routes. The yielded molecule N-[(carbamoyl-GO)ethyl]-N’-[(carbamoyl)-(2,5,7-trinitro-9-oxo-fluorene)] (GO-TNF) was thoroughly characterized and it was shown that it presents favorable highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) energy levels to function as a bridge component between the polymeric donor poly({4,8-bis[(2-ethylhexyl)oxy]benzo[1,2-b:4,5-b′]dithiophene-2,6-diyl}{3-fluoro-2-[(2-ethylhexyl)carbonyl] thieno[3,4-b]thiophenediyl}) (PTB7) and the fullerene derivative acceptor [6,6]-phenyl-C71-butyric-acid-methylester (PC71BM). In this context, a GO-TNF based ink was prepared and directly incorporated within the binary photoactive layer, in different volume ratios (1-3% ratio to the blend), for the effective realization of inverted ternary organic solar cells (OSCs) of the structure ITO/PFN/PTB7:GO-TNF:PC71BM/MoO3/Al. The addition of 2% v/v GO-TNF ink led to a champion power conversion efficiency (PCE) of 8.71% that was enhanced by ~13% as compared to the reference cell.

scholarly journals Emphasizing the Operational Role of a Novel Graphene-Based Ink into High Performance Ternary Organic Solar Cells

Nanomaterials ◽  
2020 ◽  
Vol 10 (1) ◽  
pp. 89 ◽  
Author(s):  
Minas M. Stylianakis ◽  
Dimitrios M. Kosmidis ◽  
Katerina Anagnostou ◽  
Christos Polyzoidis ◽  
Miron Krassas ◽  
...  
Keyword(s):  
Solar Cells ◽  
Molecular Orbital ◽  
Organic Solar Cells ◽  
High Performance ◽  
Energy Levels ◽  
Fullerene Derivative ◽  
Highest Occupied Molecular Orbital ◽  
Lowest Unoccupied Molecular Orbital ◽  
Synthetic Routes

A novel solution-processed, graphene-based material was synthesized by treating graphene oxide (GO) with 2,5,7-trinitro-9-oxo-fluorenone-4-carboxylic acid (TNF-COOH) moieties, via simple synthetic routes. The yielded molecule N-[(carbamoyl-GO)ethyl]-N′-[(carbamoyl)-(2,5,7-trinitro-9-oxo-fluorene)] (GO-TNF) was thoroughly characterized and it was shown that it presents favorable highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) energy levels to function as a bridge component between the polymeric donor poly({4,8-bis[(2-ethylhexyl)oxy]benzo[1,2-b:4,5-b′]dithiophene-2,6-diyl}{3-fluoro-2-[(2-ethylhexyl)carbonyl] thieno[3,4-b]thiophenediyl}) (PTB7) and the fullerene derivative acceptor [6,6]-phenyl-C71-butyric-acid-methylester (PC71BM). In this context, a GO-TNF based ink was prepared and directly incorporated within the binary photoactive layer, in different volume ratios (1%–3% ratio to the blend) for the effective realization of inverted ternary organic solar cells (OSCs) of the structure ITO/PFN/PTB7:GO-TNF:PC71BM/MoO3/Al. The addition of 2% v/v GO-TNF ink led to a champion power conversion efficiency (PCE) of 8.71% that was enhanced by ~13% as compared to the reference cell.

scholarly journals D-A-D structured organic molecules with diketopyrrolopyrrole acceptor unit for solution-processed organic solar cells

2014 ◽  
Vol 372 (2013) ◽  
pp. 20130009 ◽  
Author(s):  
Jing Zhang ◽  
Chang He ◽  
Zhi-Guo Zhang ◽  
Dan Deng ◽  
Maojie Zhang ◽  
...  
Keyword(s):  
Solar Cells ◽  
Organic Solar Cells ◽  
Organic Molecules ◽  
Bulk Heterojunction ◽  
Energy Levels ◽  
Orbital Energy ◽  
Broad Absorption ◽  
Photovoltaic Properties ◽  
Solution Processed ◽  
Highest Occupied Molecular Orbital

Four solution-processable D-A-D structured organic molecules with diketopyrrolopyrrole (DPP) as acceptor unit and triphenylamine (TPA) or (4-hexyl)thieno [3,2-b]thiophene (HTT) as donor unit, DPP8-TPA, DPP8-TPA-OR, DPP6-HTT and DPP8-HTT, were designed and synthesized for the application as donor materials in solution-processed organic solar cells (OSCs). The molecules show broad absorption and relatively lower highest occupied molecular orbital energy levels. Photovoltaic properties of the molecules were investigated by fabricating the bulk-heterojunction OSCs with the molecules as donor and PC 71 BM as acceptor. Power conversion efficiency of the OSC based on DPP8-HTT reached 1.5% under the illumination of AM1.5, 100 mW cm −2 .

Impact of side-chain fluorination on photovoltaic properties: fine tuning of the microstructure and energy levels of 2D-conjugated copolymers

2017 ◽  
Vol 5 (32) ◽  
pp. 16702-16711 ◽  
Author(s):  
Jisoo Shin ◽  
Min Kim ◽  
Boseok Kang ◽  
Jaewon Lee ◽  
Heung Gyu Kim ◽  
...  
Keyword(s):  
Solar Cells ◽  
Molecular Orbital ◽  
Polymer Solar Cells ◽  
Energy Levels ◽  
Fine Tuning ◽  
Side Chain ◽  
Photovoltaic Properties ◽  
Highly Efficient ◽  
Highest Occupied Molecular Orbital ◽  
Lowest Unoccupied Molecular Orbital

The control of the molecular energy levels of the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO) is crucial to the design of highly efficient polymer solar cells (PSCs).

Side chain modification: an effective approach to modulate the energy level of benzodithiophene based polymers for high-performance solar cells

2015 ◽  
Vol 3 (35) ◽  
pp. 18115-18126 ◽  
Author(s):  
Haimei Wu ◽  
Baofeng Zhao ◽  
Weiping Wang ◽  
Zhaoqi Guo ◽  
Wei Wei ◽  
...  
Keyword(s):  
Solar Cells ◽  
Energy Level ◽  
Conjugated Polymers ◽  
Molecular Orbital ◽  
High Performance ◽  
Bulk Heterojunction ◽  
Polymer Solar Cells ◽  
Side Chain ◽  
The Past ◽  
Highest Occupied Molecular Orbital

Over the past few years, it has been proven that deepening the highest occupied molecular orbital (HOMO) levels of conjugated polymers is one of the most successful strategies to develop novel materials for high performance bulk heterojunction polymer solar cells.

Electrochemistry, a Useful Tool in the Synthesis of Oligothiophenes

2021 ◽  
Vol 25 ◽  
Author(s):  
Fabiana Pandolfi ◽  
Martina Bortolami ◽  
Marta Feroci ◽  
Leonardo Mattiello ◽  
Vincenzo Scarano ◽  
...  
Keyword(s):  
Molecular Orbital ◽  
Organic Semiconductors ◽  
Organic Solar Cells ◽  
Field Effect Transistors ◽  
Energy Levels ◽  
Organic Field Effect Transistors ◽  
Light Emitting ◽  
Highest Occupied Molecular Orbital ◽  
Lowest Unoccupied Molecular Orbital ◽  
Organic Photodetectors

: Thiophene derivatives, either "small molecules," oligomers or polymers, play a role of primary importance among organic semiconductors. Therefore they have numerous and different technological applications in the field of Organic Electronics. For this reason, thiophene-based materials are found in devices such as organic light-emitting diodes (OLEDs), organic field-effect transistors (OFETs), organic solar cells (OSCs), organic photodetectors, and many others. Oligothiophenes and polythiophenes have in common excellent charge transport properties and synthetic procedures that are now well established. Furthermore, oligothiophenes do not possess the intrinsic disadvantages of polythiophenes, such as the lack of well-defined structures and the inevitable presence of impurities. Electrochemistry can give a significant contribution to the field of oligothiophenes not only by allowing the determination of the highest-occupied molecular orbital (HOMO) and the lowest-unoccupied molecular orbital (LUMO) energy levels by the means of cyclic voltammetry (CV), but also rendering oligothiophenes syntheses more expeditious in comparison with the classical organic ones. This review outlines the application of electrochemistry techniques to the synthesis of oligothiophene derivatives.

scholarly journals PffBT4T-2OD Based Solar Cells with Aryl-Substituted N-Methyl-Fulleropyrrolidine Acceptors

Materials ◽  
2019 ◽  
Vol 12 (24) ◽  
pp. 4100 ◽  
Author(s):  
Hugo Gaspar ◽  
Flávio Figueira ◽  
Karol Strutyński ◽  
Manuel Melle-Franco ◽  
Dzmitry Ivanou ◽  
...  
Keyword(s):  
Solar Cells ◽  
Molecular Orbital ◽  
Density Functional ◽  
Polymer Solar Cells ◽  
Energy Levels ◽  
The Novel ◽  
Functional Theory ◽  
Reduction Potentials ◽  
Highest Occupied Molecular Orbital ◽  
Lowest Unoccupied Molecular Orbital

Novel C60 and C70 N-methyl-fulleropyrrolidine derivatives, containing both electron withdrawing and electron donating substituent groups, were synthesized by the well-known Prato reaction. The corresponding highest occupied molecular orbital (HOMO)/lowest unoccupied molecular orbital (LUMO) energy levels were determined by cyclic voltammetry, from the onset oxidation and reduction potentials, respectively. Some of the novel fullerenes have higher LUMO levels than the standards PC61BM and PC71BM. When tested in PffBT4T-2OD based polymer solar cells, with the standard architecture ITO/PEDOT:PSS/Active-Layer/Ca/Al, these fullerenes do not bring about any efficiency improvements compared to the standard PC71BM system, however they show how the electronic nature of the different substituents strongly affects the efficiency of the corresponding organic photovoltaic (OPV) devices. The functionalization of C70 yields a mixture of regioisomers and density functional theory (DFT) calculations show that these have systematically different electronic properties. This electronic inhomogeneity is likely responsible for the lower performance observed in devices containing C70 derivatives. These results help to understand how new fullerene acceptors can affect the performance of OPV devices.

Optical properties of (Z)-2-(2-phenylhydrazinylidene)acenaphthen-1(2H)-one: a potential electron donor in organic solar cells

2017 ◽  
Vol 73 (6) ◽  
pp. 458-463
Author(s):  
Yan-Xiao Su ◽  
Chao-Zhi Zhang ◽  
Ming-Xia Song
Keyword(s):  
Solar Cells ◽  
Molecular Orbital ◽  
Organic Solar Cells ◽  
Energy Gap ◽  
Lumo Energy ◽  
Face To Face ◽  
Highest Occupied Molecular Orbital ◽  
Lowest Unoccupied Molecular Orbital ◽  
Title Molecule ◽  
Homo Lumo

Electron-donating molecules play an important role in the development of organic solar cells. (Z)-2-(2-Phenylhydrazinylidene)acenaphthen-1(2H)-one (PDAK), C18H12N2O, was synthesized by a Schiff base reaction. The crystal structure shows that the molecules are planar and are linked together forming `face-to-face' assemblies held together by intermolecular C—H...O, π–π and C—H...π interactions. PDAK exhibits a broadband UV–Vis absorption (200–648 nm) and a low HOMO–LUMO energy gap (1.91 eV; HOMO is the highest occupied molecular orbital and LUMO is the lowest unoccupied molecular orbital), while fluorescence quenching experiments provide evidence for electron transfer from the excited state of PDAK to C60. This suggests that the title molecule may be a suitable donor for use in organic solar cells.

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