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Efficient non-fullerene polymer solar cells enabled by side-chain conjugated thieno[3,4-c]pyrrole-4,6-dione-based polymer and small molecular acceptors
摘要： The application of non-fullerene (NF) acceptors in bulk-heterojunction (BHJ) polymer solar cells (PSCs) is a promising approach to overcome the inherent drawbacks of fullerene derivatives-based acceptors. In PSCs, complementary absorption as well as matched molecular energy levels between the low bandgap acceptor-donor-acceptor (A-D-A) small molecular acceptor and medium/wide bandgap polymer donor is crucial to achieve high power conversion efficiency (PCE). Alternating polymers based on benzodithiophene (BDT) electron-donating segment and thieno[3,4-c]pyrrole-4,6-dione (TPD) electron-withdrawing segment own medium bandgap and low-lying highest occupied molecular orbital (HOMO) energy level, leading to presentable photovoltaic properties with fullerene derivatives. To probe into the performances of TPD-based polymers in NF-PSCs, two TPD-based polymers containing alkoxy or alkylthienyl modified benzo[1,2-b:4,5-b′]dithiophene (BDT) were synthesized and adopted as electron-donors and blended with A-D-A-type electron-acceptor 2,2′-[[6,6,12,12-tetrakis(4-hexylphenyl)-s-indacenodithieno[3,2-b]thiophene]methylidyne(3-oxo-1H-indene-2,1(3H)-diylidene)]]bis(propanedinitrile) (ITIC) to fabricate the corresponding photovoltaic devices. The two-dimensional conjugated polymer PBDTT-TPD shows enhanced extinction coefficient, deeper HOMO energy level and better hole transport performance, resulting in improved PCE of 6.17%. To further boost the performances of the polymers, a small molecular acceptor 2,2′-((2Z,2′Z)-((4,4,9,9-tetrahexyl-4,9-dihydro-s-indaceno[1,2-b:5,6-b′]dithiophene-2,7-diyl) bis(methanylylidene))bis(3-oxo-2,3-dihydro-1H-indene-2,1-diylidene))dimalononitrile (IDIC) with down-shifted energy level was also used to blend with the two polymers in PSCs. Despite the open-circuit voltage (VOC) of the PBDTT-TPD:IDIC-based device is slightly decreased, the short-circuit current density (JSC) and fill factor (FF) are simultaneously improved, yielding an promising PCE of 7.15%. These results indicate that two-dimensional conjugated TPD-based polymers can be potential application as medium bandgap polymeric donor to match with small molecular acceptors having suitable molecular energy levels to get high efficiency in PSCs.
关键词： Non-fullerene acceptors,Thieno[3,4-c]pyrrole-4,6-dione,Energy level offsets,Polymer solar cells,Thermal annealing
更新于2025-09-11 14:15:04
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Bicomponent-random Approach to Synthesis of Donor Polymers for Efficient All-Polymer Solar Cells Processed from A Green Solvent
摘要： All-polymer solar cells (all-PSCs) can offer unique merits of high morphological stability to thermal and mechanical stress. To realize its full potential as flexible or wearable devices, it is highly desirable that the all-PSCs can be fabricated from green solvent with simple post-treatment to avoid thermal annealing on flexible substrate. This proposed a severely challenge on material design to tune their properties with suitable solubility, aggregation, and morphology. To address this challenge, here, a simple bicomponent-random approach on a D-A-type polymer donor was developed by just varying the D-A molar ratio. Under this approach, a series of new random polymers PBDTa-TPDb with different molar ratio of D component of 2D-benzo[1,2-b:4,5-b']dithiophene (BDT) and A component of thieno[3,4-c]pyrrole-4,6-dione (TPD) were designed and synthesized. The energy levels, light absorption, solubility and packing structure of random donors PBDTa-TPDb were found to vary substantially with the various D-A molar ratio. The devices based PBDTa-TPDb/P(NDI2HD-T) were fabricated to explore the synergistic effects of processing solvent and composition of D-A-type random polymers. The results show that nanoscale morphology, balanced miscibility/crystallinity of blend and photovoltaic properties could be rationally optimized by tuning the composition of random donors. As a result, as-cast all-PSC based optimal donor PBDT5-TPD4 achieves a best power conversion efficiency (PCE) of 8.20% processed from green solvent, which performs better than that based reference polymer (PCE: 6.41%). This efficiency is the highest value for all-PSCs from BDT-TPD-based donors. Moreover, the optimized devices exhibited relatively insensitive to the thickness of the active layer and good stability.
关键词： thieno[3,4-c]pyrrole-4,6-dione,all-polymer solar cells,bicomponent-random approach,benzo[1,2-b:4,5-b']dithiophene,green solvent
更新于2025-09-11 14:15:04
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A Novel Transparent pH Sensor Based on a Nanostructured ITO Electrode Coated with [3,3′-Co(1,2-C2B9H11)2]-Doped Poly(pyrrole)
摘要： A novel transparent and nanostructured ion-sensitive electrode based on indium tin oxide (ITO) coated with cobaltbis(dicarbollide)-doped poly(pyrrole) (PPy) is presented in this work. This metallacarborane-doped PPy was used as conducting polymer due to its high stability and chemical resistance. The ion-sensitive electrode was coupled to a miniaturized and low-cost potentiostat, in a final autonomous kit for potentiometric determination of pH. Qualitative calibration of the system revealed Nernstian behavior, resulting promising for novel point-of-care biomedical applications.
关键词： indium tin oxide (ITO),intrinsically conducting polymer (ICP),poly(pyrrole) (PPy),pH sensor,potentiometry,potentiometric sensor,boron compounds,nanoscience,metallacarboranes
更新于2025-09-10 09:29:36
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AIE-active luminogen for highly sensitive and selective detection of picric acid in water samples: Pyridyl as an effective recognition group
摘要： Detection of nitroaromatic explosives especially picric acid (PA) is considerably worth concern on human safety and homeland security. Herein, we developed an effective probe (APPTPEP) for PA detection in aqueous medium by combination of 1,4-dihydropyrrolo[3,2-b]pyrrole with tetraphenylethylene and pyridine units. The incorporation of tetraphenylethylene unit in the backbone endows the APPTPEP a significant aggregation induced emission (AIE) behavior. Pyridyl group was proved as recognition site for PA and their strong interaction was confirmed by 1H NMR titration and supported by theoretical calculation. Owing to this strong affinity, APPTPEP exhibited high selectivity and sensitivity (limit of detection 31.5 nM) to PA over other nitroaromatic compounds. This research provides new insights into the rational design of AIE-active materials for effective sensing application.
关键词： 1,4-dihydropyrrolo[3,2-b]pyrrole,Picric acid,Aggregation-induced emission,Pyridyl group
更新于2025-09-10 09:29:36
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Gold nanoparticle/nickel oxide/poly(pyrrole-N-propionic acid) hybrid multilayer film: Electrochemical study and its application in biosensing
摘要： The present study describes the fabrication of Indium Tin Oxide /gold nanoparticles/nickel oxide/poly(Pyrrole-N-propionic acid) (ITO/GNPs/NiO/poly(PPA)) multilayered film, and its modification with Tyrosinase (Ty). The ITO/GNPs/NiO/poly(PPA) electrode was fabricated by sequential electrochemical assembly onto ITO substrate which electrochemical deposition provides a facile, inexpensive technique for synthesis of multilayered film within the adherent morphology with controllable film thickness. Cyclic voltammetry (CV), Fourier transform infrared spectroscopy-attenuated total reflectance (FTIR-ATR), scanning electron microcopy (SEM), and atomic force microcopy (AFM) were used to characterize the film assembly processes. The properties of a semiconductor/electrolyte interface were investigated based on the Mott–Schottky (M-S) approach for the modified electrodes, with the flat band potential (EFB) according to the potential intercept and the carrier density (ND) according to the linear slopes. The ND and EFB of ITO/GNPs/NiO/poly(PPA) were obtained as 2.48·1021 cm–3 and 0.26 V, respectively. Tyrosinase was immobilized using carbodiimide coupling reaction. The bioelectrode was characterized by FTIR-ATR, SEM, AFM, electrochemical impedance spectroscopy (EIS). A Randles equivalent circuit was introduced for modeling the performance of impedimetric biosensing for the detection of the dopamine (DP) and the interface of bioelectrode/electrolyte. The EIS of the ITO/GNPs/NiO/poly(PPA)-Ty exhibited significant changes in the charge transfer resistance (RCT) value toward the detection of dopamine over a linear range of 80 μM to 0.2 mM with a limit of detection (LOD) of 5.46 μM.
关键词： tyrosinase,poly(pyrrole-N-propionic acid),polymer composites,Mott–Schottky,dopamine
更新于2025-09-09 09:28:46
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Mechanoresponsive Material of AIE-Active 1,4-Dihydropyrrolo[3,2-b]pyrrole Luminophores Bearing Tetraphenylethylene Group with Rewritable Data Storage
摘要： A new tetraphenylethylene (TPE) functionalized 1,4-dihydropyrrolo[3,2-b]pyrrole derivative (APPTPECN) was synthesized with obvious aggregation-induced emission (AIE) active by simple synthetic method. APPTPECN exhibited reversible mechano?uorochromic (MFC) behavior. The powder X-ray diffraction (PXRD) and scanning electron microscopy (SEM) investigations exhibited that the MFC nature is originated through a conversion from the microcrystalline to amorphous phase under the stimulus of external force. The results obtained would be of major help in understanding the MFC mechanism and designing new MFC materials. Compound APPTPECN has the potential possibility to employ in rewritable data storage and is of assistance in the rational design of smart luminescent materials.
关键词： rewritable data storage,reversible mechanochromism behavior,aggregation-induced emission (AIE),1,4-dihydropyrrolo[3,2-b]pyrrole derivative
更新于2025-09-04 15:30:14
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Fluorescence Behavior of Bis(cyanostyryl)pyrrole Derivatives Depending on Substituent Position of Cyano Groups in Solution and in Solid State
摘要： We synthesized a novel fluorophores of distyrylpyrrole derivatives possessing cyano groups at different position on olefin. Their fluorescence properties in solution and solid state were investigated by photoluminescence quantum yield and lifetime measurement, which provided radiative decay constant (kf) and nonradiative decay constant (knr). The derivative with cyano groups at inner position of molecule, inner isomer, shows high fluorescence quantum yield (Φf = 0.43) in solution while another derivative with cyano group at outer position, outer isomer, hardly shows fluorescence (Φf < 0.01) due to the large nonradiative decay (knr > 10 ns?1). Upon formation of single crystal or nanoparticles, these difference were inverted; the quantum yield of outer and inner isomer was enhanced and diminished, respectively. We explained these differences between in solution and solid state by means of analysis of single X-ray structure and computation study.
关键词： solid emission,pyrrole derivatives,substituent effect,Solid-state luminescence enhancement
更新于2025-09-04 15:30:14