0000000000261193

AUTHOR

Haijun Xu

showing 6 related works from this author

Two-Photon Absorption Properties and Structures of BODIPY and Its Dyad, Triad and Tetrad.

2018

A series consisting of a dyad, a triad and a tetrad containing either two, three and four BODIPY units, respectively, has been synthesized and fully characterized and compared to two mono-BODIPY analogs (used as references). The one- and two-photon photophysical properties have been measured and the X-ray structures of four of the BODIPY derivatives have been determined. In the 700-900 nm range, the two-photon absorption (TPA) cross sections range from 30 GM to 160 GM for these compounds.

010405 organic chemistryChemistryTriad (anatomy)General Chemistry010402 general chemistry01 natural sciencesTwo-photon absorption0104 chemical scienceschemistry.chemical_compoundCrystallographymedicine.anatomical_structuremedicineBODIPYAbsorption (chemistry)TetradChemPlusChem
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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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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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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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Efficient energy transfer in a tri-chromophoric dyad containing BODIPYs and corrole based on a truxene platform

2018

A star-shaped molecule was designed and synthesized based on a known central truxene platform. Two BODIPY derivatives and one corrole macrocycle were introduced and connected to the 2, 7 and 12-positions of the truxene unit by Suzuki coupling. The dyad was fully characterized by UV-vis absorption, proton nuclear magnetic resonance, mass spectrometry. The direction of energy transfer upon electronic excitation was explored, and the star-shaped molecule system exhibits a highly efficient photoinduced energy transfer process from the excited BODIPY part to the corrole unit.

chemistry.chemical_compound010405 organic chemistryChemistryEnergy transferMoleculeGeneral ChemistryCorroleBODIPY010402 general chemistry01 natural sciencesCombinatorial chemistry0104 chemical sciencesEfficient energy useJournal of Porphyrins and Phthalocyanines
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Synthesis of flexible nanotweezers with various metals and their application in carbon nanotube extraction

2018

Bisporphyrin-based flexible nanotweezers with various metals were synthesized and applied to the extraction of single-walled carbon nanotubes. Homo- and hetero-metallic bisporphyrins containing Co2+ were found to afford higher SWNT-extraction ability, while no or a little amount of SWNTs were extracted by bisporphyrins with other metals.

ChemistryExtraction (chemistry)02 engineering and technologyGeneral ChemistryCarbon nanotube010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesCatalysis0104 chemical scienceslaw.inventionChemical engineeringlawMaterials Chemistry0210 nano-technologyNew Journal of Chemistry
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