0000000001319414

AUTHOR

Ganesh D. Sharma

showing 14 related works from this author

Nonfullerene Polymer Solar Cells Reaching a 9.29% Efficiency Using a BODIPY-Thiophene Backboned Donor Material

2018

A conjugated polymer donor containing BODIPY-thiophene dyads in the backbone, P(BdP-EHT), combined with a low bandgap nonfullerene acceptor (SMDPP) consisting of carbazole and diketopyrrolopyrrole units linked with a tetracyanobutadiene acceptor π-linker, was used to design bulk heterojunction polymer solar cells. After the optimization of the donor to acceptor weight ratio and solvent vapor annealing of the P(BdP-EHT):SMDPP active layer, the resulting polymer solar cell showed an overall power conversion efficiency of 9.29%, which is significantly higher than that for the polymer solar cell based on PC71BM (7.41%) processed under identical conditions. This improved power conversion efficie…

Materials scienceOrganic solar cellOpen-circuit voltageCarbazoleEnergy conversion efficiencyEnergy Engineering and Power Technology02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry7. Clean energy01 natural sciencesAcceptorPolymer solar cell0104 chemical scienceschemistry.chemical_compoundchemistryMaterials ChemistryElectrochemistryChemical Engineering (miscellaneous)Electrical and Electronic Engineering0210 nano-technologyHOMO/LUMOShort circuitACS Applied Energy Materials
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New BODIPY derivatives with triarylamine and truxene substituents as donors for organic bulk heterojunction photovoltaic cells

2021

Abstract We have designed two new BODIPY derivatives, denoted as 6a and 6b, substituted with truxene moiety and triphenylamine (TPA) unit groups and have investigated their optical and electrochemical properties. Dyes 6a and 6b were employed as donor along with PC71BM or Y6 as acceptor for the fabrication of binary and ternary organic solar cells. After optimization of the binary and ternary active layers, we have achieved over all power conversion efficiency (PCE) of 11.37 % and 13.32% for 6a:PC71BM:Y6 and 6b:PC71BM:Y6 ternary organic solar cells, respectively, which are higher than the binary organic solar cells based on PC71BM or Y6 acceptor. The higher power conversion efficiency for te…

Materials scienceOrganic solar cellRenewable Energy Sustainability and the EnvironmentEnergy conversion efficiencyPhotochemistryTriphenylamineAcceptorPolymer solar cellchemistry.chemical_compoundchemistryMoietyGeneral Materials ScienceBODIPYTernary operationSolar Energy
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A bacteriochlorin-diketopyrrolopyrrole triad as a donor for solution-processed bulk heterojunction organic solar cells

2019

We have designed an A–π–D–π–A small-molecule triad consisting of a bacteriochlorin (BC) donor central core linked with two diketopyrrolopyrrole (DPP) acceptors via ethynyl bridges (BC-DPP-1). BC-DPP-1 has a narrow optical bandgap of 1.38 eV with highest occupied molecular orbital and lowest unoccupied molecular orbital energy levels of −4.93 eV and −3.40 eV, respectively, and it was used as an electron donor along with [6,6]-phenyl-C71-butyric acid methyl ester (PC71BM) as an acceptor for solution-processed small-molecule organic solar cells. After optimizing the weight ratio between BC-DPP-1 and PC71BM and pyridine as a solvent additive and subsequent solvent vapor annealing using THF, an …

Materials scienceOrganic solar cellBand gapPhotovoltaic systemEnergy conversion efficiencyAnalytical chemistry02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology7. Clean energy01 natural sciencesAcceptorPolymer solar cell0104 chemical sciencesMaterials Chemistry0210 nano-technologyTernary operationHOMO/LUMOJournal of Materials Chemistry C
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Polymer solar cell based on ternary active layer consists of medium bandgap polymer and two non-fullerene acceptors

2020

Abstract An efficient PSCs consisting of a ternary active layer containing a medium bandgap conjugated polymer P and two well-known non-fullerene acceptors i.e. ITIC-m and Y6 was fabricated. An overall Power Conversion Efficiency (PCE) of about 15.13% was achieved, with the optimized ternary active layer consisting of 20 wt% of ITIC-m in acceptors i.e. P:ITIC-m:Y6 (1:0.3:1.2). This value is higher than that for the binary counter parts i.e. 12.10% and 13.16% for P:ITIC-m (1:1.5 w:w) and P:Y6 (1:1.5 w:w). The higher short circuit current density of the ternary active layer PSCs is related to the broader absorption spectra as compared to the binary active layer analogs. The open circuit volta…

Materials scienceRenewable Energy Sustainability and the EnvironmentBand gapOpen-circuit voltage020209 energyAnalytical chemistry02 engineering and technology021001 nanoscience & nanotechnologyAcceptorPolymer solar cellActive layer0202 electrical engineering electronic engineering information engineeringGeneral Materials Science0210 nano-technologyTernary operationShort circuitHOMO/LUMOSolar Energy
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Porphyrins and BODIPY as Building Blocks for Efficient Donor Materials in Bulk Heterojunction Solar Cells

2017

International audience; Advances in the synthesis and application of highly efficient polymers and small molecules over the last two decades have enabled the rapid advancement in the development of organic solar cells and photovoltaic technology as a promising alternative to conventional solar cells, based on silicon and other inorganic semiconducting materials. Among the different types of organic semiconducting materials, porphyrins and BODIPY-based small molecules and conjugated polymers attract high interest as efficient semiconducting organic materials for dye sensitized solar cells and bulk heterojunction organic solar cells. The highest power conversion efficiency exceeding 9% has be…

Materials scienceOrganic solar cellEnergy Engineering and Power Technologypower-conversion efficiency02 engineering and technologydonor materials010402 general chemistryporphyrins7. Clean energy01 natural sciencesPolymer solar cellbulk heterojunction solar cellsphotoinduced electron-transferchemistry.chemical_compoundBODIPYElectrical and Electronic Engineeringsmall-moleculelow-bandgap polymerbusiness.industryfield-effect transistors[CHIM.MATE]Chemical Sciences/Material chemistryHybrid solar cellpi-conjugated copolymersd-a021001 nanoscience & nanotechnologyAtomic and Molecular Physics and Optics0104 chemical sciencesElectronic Optical and Magnetic Materialsphotovoltaic propertieschemistryopen-circuit voltage[ CHIM.MATE ] Chemical Sciences/Material chemistryOptoelectronicsorganic photovoltaicsBODIPY0210 nano-technologybusiness
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Photovoltaic Properties of a Porphyrin-Containing Polymer as Donor in Bulk Heterojunction Solar Cells With Low Energy Loss

2017

chemistry.chemical_classificationMaterials sciencebusiness.industryPhotovoltaic systemEnergy conversion efficiencyEnergy Engineering and Power Technology02 engineering and technologyPolymer010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesPorphyrinAtomic and Molecular Physics and OpticsPolymer solar cell0104 chemical sciencesElectronic Optical and Magnetic Materialschemistry.chemical_compoundLow energychemistryOptoelectronicsElectrical and Electronic Engineering0210 nano-technologybusinessSolar RRL
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BODIPY–diketopyrrolopyrrole–porphyrin conjugate small molecules for use in bulk heterojunction solar cells

2018

Two small molecules denoted as BD-pPor and BD-tPor composed of a central BODIPY core surrounded with two DPP and two porphyrin units have been designed and synthesized. In BD-pPor and BD-tPor, porphyrins are linked to the central BODIPY by phenyl and thiophene bridges, respectively. The optical and electrochemical properties were systematically investigated in order to employ them as donors along with PC71BM as an acceptor for solution processed bulk heterojunction organic solar cells. After the optimization of the active layer, the organic solar cells based on BD-pPor and BD-tPor exhibit overall power conversion efficiencies of 6.67% and 8.98% with an energy loss of 0.63 eV and 0.50 eV. Th…

Materials scienceOrganic solar cell02 engineering and technology010402 general chemistryPhotochemistry7. Clean energy01 natural sciencesPolymer solar cellchemistry.chemical_compound[CHIM.ANAL]Chemical Sciences/Analytical chemistryThiopheneGeneral Materials Science[CHIM.COOR]Chemical Sciences/Coordination chemistryHOMO/LUMOComputingMilieux_MISCELLANEOUSRenewable Energy Sustainability and the Environment[CHIM.ORGA]Chemical Sciences/Organic chemistryGeneral Chemistry[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnologySmall moleculeAcceptorPorphyrin0104 chemical scienceschemistryBODIPY0210 nano-technology
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Ternary Organic Solar Cell with a Near‐Infrared Absorbing Selenophene–Diketopyrrolopyrrole‐Based Nonfullerene Acceptor and an Efficiency above 10%

2020

Materials scienceOrganic solar cellNear-infrared spectroscopyEnergy Engineering and Power TechnologyElectrical and Electronic EngineeringPhotochemistryTernary operationAcceptorAtomic and Molecular Physics and OpticsElectronic Optical and Magnetic MaterialsSolar RRL
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High-efficiency fullerene free ternary organic solar cells based with two small molecules as donor

2021

Abstract Herein, we have designed a ternary system comprising of two small molecules (B2 and B3), as donor and a narrow bandgap non-fullerene small molecule acceptor Y6. The chemical structures of B2 and B3 are close to each other but their absorption spectra are complementary with different energy levels. Using these small-molecules, a ternary organic solar cell was fabricated. The presence of B2 in the B3:Y6 blend increases the photon harvesting as well as also forms cascade energy level arrangement which benefits assisting the balancing between the dissociation of excitons into free charge carriers and their subsequent charge transfer between the two donors (B2 and B3) and the acceptor (…

Materials scienceTernary numeral systemPhotoluminescenceOrganic solar cellAbsorption spectroscopyBand gapOrganic Chemistry02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciencesAcceptorAtomic and Molecular Physics and Optics0104 chemical sciencesElectronic Optical and Magnetic MaterialsInorganic ChemistryCharge carrierElectrical and Electronic EngineeringPhysical and Theoretical Chemistry0210 nano-technologyTernary operationSpectroscopyOptical Materials
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Synthesis and characterization of zinc carboxy–porphyrin complexes for dye sensitized solar cells

2018

Two zinc porphyrins, 2 and 8, have been synthesized. Porphyrin 8 displays better electronic communication between the dye and the TiO2 electrode. Photophysical measurements and electrochemistry experiments suggest that both porphyrins are very promising sensitizers for dye-sensitized solar cells (DSSCs). It was found that their molecular orbital energy levels favor electron injection and dye regeneration in DSSCs. Solar cells sensitized by 2 and 8 were fabricated, and it was found that they show power conversion efficiencies (PCEs) of 5.27% and 7.13%, respectively. Photovoltaic measurements (J–V curves) together with the incident photon-to-electron conversion efficiency spectra of the two c…

Energy conversion efficiencyPhotovoltaic systemchemistry.chemical_element02 engineering and technologyGeneral ChemistryZinc010402 general chemistry021001 nanoscience & nanotechnologyElectrochemistryPhotochemistry01 natural sciencesPorphyrinElectron transport chainCatalysis0104 chemical sciencesDye-sensitized solar cellchemistry.chemical_compoundchemistryElectrodeMaterials Chemistry0210 nano-technologyNew Journal of Chemistry
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Carbazole-based green and blue-BODIPY dyads and triads as donors for bulk heterojunction organic solar cells.

2020

Two BODIPY derivatives with one (B2) and two (B3) carbazole moieties were synthesized and applied as electron-donor materials in organic photovoltaic cells (OPV). Their optical and electrochemical properties were systematically investigated. These BODIPY dyes exhibit excellent solubility in organic solvents and present high molar extinction coefficients (1.37–1.48 × 105 M−1 cm−1) in solutions with absorption maxima at 586 nm for mono-styryl groups and at 672 nm for di-styryl groups. The introduction of the styryl moieties results in a large bathochromic shift and a significant decrease in the HOMO–LUMO energy-gaps. The BODIPY dyes show relatively low HOMO energies ranging from −4.99 to −5.1…

Inorganic Chemistrychemistry.chemical_compoundMaterials sciencechemistryOrganic solar cellCarbazoleBathochromic shiftMolecular orbitalCyclic voltammetryBODIPYPhotochemistryAcceptorPolymer solar cellDalton transactions (Cambridge, England : 2003)
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Porphyrin Antenna-Enriched BODIPY–Thiophene Copolymer for Efficient Solar Cells

2018

International audience; Low bandgap A−π–D copolymer, P(BdP-DEHT), consisting of alternating BOronDIPYrromethene (BODIPY) and thiophene units bridged by ethynyl linkers, and its porphyrin-enriched analogue, P(BdP/Por-DEHT), were prepared, and their optical and electrochemical properties were studied. P(BdP-DEHT) exhibits strong absorption in the 500–800 nm range with an optical bandgap of 1.74 eV. On the basis of cyclic voltammetry, the highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) energy levels are evaluated to be −5.40 and −3.66 eV, respectively. After the anchoring of zinc(II) porphyrin on the BODIPY unit, P(BdP/Por-DEHT) displays broadened absor…

Materials scienceBand gap02 engineering and technology010402 general chemistry01 natural sciences7. Clean energyPolymer solar cellporphyrin substitutionDichlorobenzenechemistry.chemical_compoundThiopheneGeneral Materials ScienceHOMO/LUMOsolvent vapor annealing[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnologyPorphyrin0104 chemical sciencespower conversion efficiencyCrystallographyApiD copolymerchemistry[ CHIM.MATE ] Chemical Sciences/Material chemistryBODIPYCyclic voltammetry0210 nano-technologypolymer solar cells
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A Very Low Band Gap Diketopyrrolopyrrole-Porphyrin Conjugated Polymer

2017

International audience; A porphyrin-diketopyrrolopyrrole-containing polymer (poly(porphyrin-diketopyrrolopyrrole) (PPDPP)) shows impressive molar absorption coefficients from lambda=300 to 1000 nm. The photophysical and structural properties of PPDPP have been studied. With PPDPP as the electron donor and [ 6,6]phenyl C-71 butyric acid methyl ester (PC71BM) as the electron acceptor, the bulk heterojunction polymer solar cell showed overall power conversion efficiencies of 4.18 and 6.44% for as-cast and two-step annealing processed PPDPP: PC71BM (1: 2) active layers, respectively. These results are quite impressive for porphyrin-containing polymers, especially when directly included in the p…

Materials scienceBand gapbuilding-blockporphyrinoidsElectron donorthin-film transistors02 engineering and technologyConjugated system010402 general chemistryPhotochemistry[ CHIM ] Chemical Sciences01 natural sciencesPolymer solar cellheterojunction solar-cellschemistry.chemical_compound[CHIM]Chemical Sciencessmall-moleculepolymerschemistry.chemical_classificationsemiconducting polymerscharge transferGeneral ChemistryPolymerChromophoreElectron acceptorside-chains021001 nanoscience & nanotechnologyPorphyrinphotovoltaic properties0104 chemical sciencesphotodynamic therapychemistryorganic photovoltaics0210 nano-technologyabsorptionperformanceconjugationChemPlusChem
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CCDC 1910052: Experimental Crystal Structure Determination

2019

Related Article: Flavien Ponsot, Léo Bucher, Nicolas Desbois, Yoann Rousselin, Pritam Mondal, Charles H. Devillers, Anthony Romieu, Claude P. Gros, Rahul Singhal, Ganesh D. Sharma|2019|J.Mater.Chem.C|7|9655|doi:10.1039/C9TC02724F

717-dibromo-5-methoxy-221212-tetramethyl-231213-tetrahydroporphyrinSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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