- 标题
- 摘要
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- 实验方案
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Hollow hierarchical structure Co0.85Se as efficient electrocatalyst for the triiodide reduction in dye-sensitized solar cells
摘要： The exploration of nonprecious metal-based electrocatalysts with high efficiency for the triiodide reduction is critical for the practical applications of the dye-sensitized solar cells. Herein, we develop a facile one-step hydrothermal method to synthesize hollow hierarchical structure Co0.85Se. Under the methanol-water reaction system, the product named as hollow hierarchical structure Co0.85Se-M has the largest specific surface area (215.36 m2 g?1) and the best crystallinity than other products obtained from other alcohol-water reaction systems. When this electrocatalyst is applied as a counter electrode for the dye-sensitized solar cells, it exhibits a small peak-to-peak separation (Epp, 97 mV) for the reduction of I3?/I? redox couple. It is found that the catalytic activity of Co0.85Se is closely dependent on the crystallinity. Moreover, the reactivity pathway is identified by density functional theory, which confirms that triiodide is reduced to iodide ion on Co0.85Se with a smaller energy barrier (～0.65 eV) than on Pt (～1.18 eV). Both experimental and theoretical results demonstrate Co0.85Se-M as an ideal counter electrode material for the dye-sensitized solar cells with a higher power conversion efficiency (8.76%) than Pt counter electrode (7.20%).
关键词： Dye-sensitized solar cells,Hollow hierarchical structure,Cobalt selenides,Electrocatalytic activity,Triiodide reduction
更新于2025-11-21 11:03:13
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Solar cells sensitized with porphyrin dyes with a carbazole donor: The effects of an auxiliary benzothiadiazole acceptor and bulky substituents on the donor
摘要： Three porphyrin sensitizers XW54–XW56 containing a carbazole donor have been designed and synthesized by introducing a benzothiadiazole (BTD) unit as the auxiliary electron acceptor to extend the absorption spectra and/or bulky dihexyloxyphenyl groups into the carbazole unit to suppress dye aggregation and improve the photovoltage (Voc). The BTD unit incorporated in XW54 obviously broadens and red-shifts the absorption threshold to ca. 700 nm, as compared with that of 650 nm observed for XW1. Thus, XW54 exhibits a much broader monochromatic photon-to-electron conversion efficiency (IPCE) spectrum with an extremely red-shifted onset wavelength of 780 nm, resulting in a photocurrent density (Jsc) of 11.60 mA cm?2, higher than that of XW1. Unfortunately, the Voc value was decreased owing to the more severe dye aggregation caused by the large conjugation framework induced by the presence of the BTD unit. As a result, XW54 shows an efficiency of 6.26%, slightly higher than that of 6.11% obtained for XW1. On the other hand, with the bulky dihexyloxyphenyl donor groups introduced to XW55, a highest Voc of 860 mV was achieved, which can be ascribed to the efficient prevention of charge recombination and suppression of dye aggregation. Thus, XW55-based cells exhibit an improved e?ciency of 6.60%. On the basis of XW54 and XW55, two bulky dihexyloxyphenyl groups and a BTD unit were simultaneously introduced to XW56, affording a highest efficiency of 7.03%, with the Jsc and Voc values of 12.5 mA cm?2 and 785 mV, respectively. These results compose a novel approach for developing e?cient dye-sensitized solar cells (DSSCs) by simultaneously introducing bulky dihexyloxyphenyl groups and a benzothiadiazole unit, which may synergistically broaden the absorption spectra and suppress the dye aggregation, resulting in improved photocurrent and photovoltage.
关键词： Dye-sensitized solar cells,Sensitizers,Porphyrin,Bulky groups,Carbazole
更新于2025-11-19 16:56:42
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Colloidally synthesized defect-rich $$\hbox {MoSe}_{2}$$ MoSe 2 nanosheets for superior catalytic activity
摘要： Transition metal dichalcogenide (TMD) nanosheets (NSs) with defect-rich and vertically aligned edges are highly advantageous for various catalytic applications. However, colloidal synthesis of defect-rich NSs with thickness variation has been a challenging task. Here, we report a colloidal synthesis of 2H-MoSe2 NSs having a large number of defects and vertically aligned edges, where the thickness is varied by changing the amount of coordinating solvent. The Se-vacancies in these NSs have introduced defect sites which are corroborated by the presence of additional vibration modes in Raman spectra. These NSs exhibit electrocatalytic hydrogen evolution reaction performances with a low overpotential (210–225 mV) at 10 mA cm?2 current density and a small Tafel slope (54–68 mV per decade). Moreover, these MoSe2 NSs are also employed as counter electrodes (CEs) for the fabrication of dye sensitized solar cells via a cost-effective and simplified procedure. The power conversion efficiencies of 7.02 ± 0.18%, comparable with Pt CE (7.84 ± 0.10%) could be routinely achieved. These results demonstrate a novel synthetic strategy to prepare layered TMDs with superior catalytic applications.
关键词： counter electrode,Transition metal dichalcogenides,dye sensitized solar cells,MoSe2 nanosheets,hydrogen evolution reaction
更新于2025-11-19 16:56:35
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Dual-band luminescent solar converter-coupled dye-sensitized solar cells for high performance semi-transparent photovoltaic device
摘要： We demonstrate a high-performance semi-transparent solar cell using a dye-sensitized solar cell (DSSC) coupled with a luminescent solar converter (LSC) that absorbs a dual band. We present an architecture of a sandwich-type, downshift (DS) LSC / DSSC / upconversion (UC) LSC. The DS LSC, including anthracene, converts ultraviolet light to visible light, and the UC LSC, which contains a dye pair of meso-tetraphenyl-tetrabenzoporphine palladium / 9,10-bis-penylethynyllanthrancane, converts near-infrared light into visible light. Thus, the dual band LSC improved the power conversion efficiency (PCE) of the DSSC without a significant decrease in visible transmittance. We optimize the concentration of the fluorescence dye to obtain maximum photoluminescence in each LSC. We also optimize backward scattering by introducing nanoparticle scatterers in UC LSC. The dual LSC-DSSC showed an average visible transmittance of 42% and achieved an PCE of up to 7.8%. Our incorporation of broadband-wavelength-harvestable LSCs with a DSSC presents a direction for semi-transparent photovoltaic devices.
关键词： Luminescence solar concentrator,Semi-transparent photovoltaic devices,Downshift,Photon upconversion,Dye-sensitized solar cells
更新于2025-11-19 16:46:39
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Formation of CoTe2 embedded in nitrogen-doped carbon nanotubes-grafted polyhedrons with boosted electrocatalytic properties in dye-sensitized solar cells
摘要： Developing high active and earth-abundant electrocatalysts is a challenge for commercialization of dye-sensitized solar cells (DSSCs). Herein, a designed synthesis of CoTe2 nanoparticles embedded in nitrogen-doped carbon nanotubes-grafted polyhedron (CoTe2@NCNTs) using zeolitic imidazolate framework-67 (ZIF-67) as template is reported. Benefiting from the high surface area induced by the in situ growth of CNTs and the synergistic effect between CoTe2 and the N-doped nanostructured carbon, CoTe2@NCNTs hybrids exhibit remarkable catalytic activity toward the reduction of I3? ions. When employed as counter electrode (CE) of DSSCs, CoTe2@NCNTs hybrids deliver overwhelming power conversion efficiency (PCE) of 9.02%, possessing ~12% improvement compared with the Pt CE (8.03%). This study provides an emerging substitute for traditional Pt CE and a strategy to synthesize efficient electrocatalysts via rational surface engineering.
关键词： Carbon nanotubes,Counter electrode,Dye-sensitized solar cells,Cobalt telluride
更新于2025-11-14 17:04:02
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Hierarchical TiO <sub/>2</sub> microspheres composed with nanoparticle-decorated nanorods for the enhanced photovoltaic performance in dye-sensitized solar cells
摘要： Hierarchical TiO2 microspheres composed of nanoparticle-decorated nanorods (NP-MS) were successfully prepared with a two-step solvothermal method. There were three benefits associated with the use of NP-MS as a photoanode material. The decoration of nanoparticles improved the specific surface area and directly enhanced the dye loading ability. Rutile nanorods serving as electron transport paths resulted in fast electron transport and inhibited the charge recombination process. The three-dimensional hierarchical NP-MS structure supplied a strong light scattering capability and good connectivity. Thus, the hierarchical NP-MS combined the beneficial properties of improved scattering capability, dye loading ability, electron transport and inhibited charge recombination. Attributed to these advantages, a photoelectric conversion efficiency of up to 7.32% was obtained with the NP-MS film-based photoanode, resulting in a 43.5% enhancement compared to the efficiency of the P25 film-based photoanode (5.10%) at a similar thickness. Compared to traditional photoanodes with scattering layers or scattering centers, the fabrication process for single layered photoanodes with enhanced scattering capability was very simple. We believe the strategy would be beneficial for the easy fabrication of efficient dye-sensitized solar cells.
关键词： electron transport,dye-sensitized solar cells,solvothermal method,Hierarchical TiO2 microspheres,photovoltaic performance
更新于2025-11-14 17:04:02
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Carbon Black and Titanium Interlayers Between Zinc Oxide Photo Electrode and Fluorine-Doped Tin Oxide for Dye-Sensitized Solar Cells
摘要： Carbon black and titanium interlayers were deposited on ?uorine-doped tin oxide (FTO) anode layers using radio frequency magnetron sputtering method. On top of them, Zinc oxide (ZnO) photo anode layers were prepared using plasma enhanced chemical vapor deposition technique. ZnO high binding energy as well as good breakdown strength, cohesion, and stability used as a photo electrode material for dye-sensitized solar cells (DSSC), but it does not have a good electrical contact to the FTO anode. To solve this problem, the carbon black and titanium interlayers were deposited. The effect of interlayers on the power conversion ef?ciency (PCE) of DSSCs was investigated. The PCE of the devices with 120-nm-thick interlayers of carbon black or titanium was 5.21 or 4.45%, respectively, which were larger than the PCE of the devices without such interlayers (3.25%). The smooth interface of the carbon black interlayer reduced the interface impedance of the ZnO photo anode effectively. On the other hand, the titanium interlayer with TiO2 on the ZnO side increased the impedance, and decreased the PCE.
关键词： Fluorine-Doped Tin Oxide,Titanium,Carbon Black,Dye-Sensitized Solar Cells
更新于2025-11-14 17:04:02
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Synthesis of porous NiMo sulphide microspheres for high-Performance dye-sensitized solar cells and supercapacitor
摘要： Novel hierarchical porous NiMoS4 microspheres with high electrochemical performance was successfully prepared using a facile one-step hydrothermal method. The dual application of porous NiMoS4 microspheres in energy harvesting and storage (ie, dye-sensitized solar cells (DSSCs) and supercapacitors (SCs) respectively) is explored. In contrast to NiS2 nanosheets, MoS2 nanosheets and Pt counter electrodes (CEs), the NiMoS4 microspheres CE demonstrated the lowest charge transfer resistance and highest electrocatalytic activity for the I3?/I? redox couple reaction. The NiMoS4-based DSSC showed a high power conversion efficiency (8.9%) even than that of Pt-based DSSC (8.7%) under simulated standard global AM 1.5G sunlight (100 mW cm?2). As an electroactive material for SCs, the assembled NiMoS4//AC asymmetric supercapacitor showed excellent specific capacitance (118.7 F g?1 at 1 A g?1), high energy density of 42.2 Wh kg?1 (with a power density of 799.2 W kg?1), and superior cycling durability with a specific capacitance retention of 79.5% after 9000 cycles at 3 A g?1.
关键词： Asymmetric supercapacitor,Ni-Mo sulfide,Microspheres,Dye-sensitized solar cells
更新于2025-11-14 17:04:02
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Synthesis of CoNi bimetallic alloy nanoparticles wrapped in nitrogen-doped graphite-like carbon shells and their electrocatalytic activity when used in a counter electrode for dye-sensitized solar cells
摘要： Nanoparticles of the bimetallic alloy CoNi wrapped in nitrogen-doped graphite-like carbon shells and dispersed on nitrogen-doped graphite-like carbon sheets (CoxNi1?x@NC) were synthesized by calcining CoNi metal–organic frameworks that were prepared through a facile solvothermal reaction using various raw-material molar ratios Co:Ni and CoNi:ethylenedinitrilotetraacetic acid. After depositing CoxNi1?x@NC for use as a counter electrode film in dye-sensitized solar cells, it was found that the electrocatalytic activity of the CoxNi1?x@NC counter electrode towards triiodide reduction could be optimized by simply tuning the molar ratios (Co:Ni and CoNi:ethylenedinitrilotetraacetic acid) appropriately during CoxNi1?x@NC synthesis. Cells that utilized a CoxNi1?x@NC counter electrode exhibited strong chemical-composition-dependent photovoltaic performance. Under optimal conditions, the CoxNi1?x@NC counter electrode presented an impressive energy conversion efficiency of 3.58%, suggesting that it is a highly promising counter electrode for application in dye-sensitized solar cells. This counter electrode has the advantages that it is considerably less expensive than a Pt counter electrode and that it provides the basis for the design and preparation of other inexpensive and efficient counter electrodes to replace Pt.
关键词： Photovoltaic performance,Dye-sensitized solar cells,CoNi alloy bimetallic nanoparticles,Counter electrode,Electrocatalytic activity
更新于2025-11-14 17:04:02
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In situ synthesis of ternary nickel iron selenides with high performance applied in dye-sensitized solar cells
摘要： Comparing with the binary chalcogenides, the ternary chalcogenides may achieve higher electrical conductivity and electrochemical activity due to the synergistic effect of the different metal cations. Herein, ternary nickel iron selenide (Ni0.5Fe0.5Se2) was fabricated through a facile one-pot solvothermal method with the assistance of glucose for the first time. The dye-sensitized solar cells (DSSCs) were assembled with the as-prepared Ni0.5Fe0.5Se2 as counter electrode (CE). Electrochemical measurements indicated that the Ni0.5Fe0.5Se2 possessed small electron transfer resistance at the interface between electrode and electrolyte, great electrocatalytic activity and reaction kinetics toward the reduction of triiodide. Compared with conventional Pt CE (7.24%), the DSSCs based on Ni0.5Fe0.5Se2 CE achieved a greater power conversion efficiency of 7.89%. Furthermore, this study provides a new idea and strategy with convenient method to synthesize Pt-free alternative materials.
关键词： Counter electrode,Solvothermal method,Dye-sensitized solar cells,Ternary nickel iron selenide
更新于2025-11-14 17:04:02