Comparative study between dye-sensitized and CdS quantum-dots-sensitized TiO2 solar cells using photoinduced absorption spectroscopy

Two 8 μm thick TiO2 photoelectrodes have been sensitized sep. by N719 dye mols. and CdS quantum dots for a comparison study. Photoinduced absorption (PIA) spectroscopy was employed to investigate the mechanistic properties of electrons under illumination conditions comparable to sunlight. The PIA spectrum of both electrodes (in the presence of electrolyte) is due to electrons in TiO2 and iodine radicals I2- in the electrolyte. In the absence of redox electrolyte, both electrodes show long-lived photoinduced charge-sepn. with lifetime in a millisecond range (8.5 ms for Q-dot-sensitized TiO2 and 11.5 ms for dye-sensitized TiO2)

FeS2-quantum-dot sensitized metal oxide photoelectrodes: photoelectrochemistry and photoinduced absorption spectroscopy

TiO2, ZnO nanoparticulate(-np), and ZnO-nanorod(-nr) electrodes have been modified with FeS2 (pyrite) nanoparticles. Quantum size effect is manifested by a blue shift in both absorption and photocurrent action spectra. PIA (photoinduced absorption spectroscopy), a multipurpose tool in the study of dye-sensitized solar cells, is used to study quantum-dot modified metal oxide (MO) nanostructured electrodes. The PIA spectra showed an evidence for long-lived photoinduced charge sepn. Time-resolved PIA showed that recombination between electrons and holes occurs on a millisecond timescale. Incident-photon-to-current efficiencies at 400 nm are ranged between 13% and 25%. The better solar cell performance of FeS2 on ZnO-nr over ZnO-np can be ascribed to the faster, unidirectional e-transport channels through the ZnO-nr as well as the longer electron lifetimes. The lower performances of electrodes can be explained by the presence of FeS2 phases other than the photoactive pyrite phase, as evidenced from XRD study

Structural, Thermal, and Electrical Properties of Poly(Ethylene Oxide)—Tetramethyl Succinonitrile Blend for Redox Mediators

An all-solid–state dye-sensitized solar cell is one of the non-fossil fuel-based electrochemical devices for electricity generation in a high-temperature region. This device utilizes a redox mediator, which is a fast ion-conducting solid polymer electrolyte (SPE). The SPE makes the device economical, thinner, and safer in high-temperature regions. The SPE generally has a form of matrix−plasticizer−redox salts. Succinonitrile (SN) is generally employed as a plasticizer for reducing the crystallinity of poly(ethylene oxide), abbreviated as PEO, a common polymeric matrix. In the present paper, the structural and thermal properties of tetramethyl succinonitrile (TMSN) were compared with SN for its application as a solid plasticizer. TMSN and SN both are plastic crystals. TMSN has four methyl groups by replacing the hydrogen of the SN, resulting in higher molecular weight, solid–solid phase transition temperature, and melting temperature. We thoroughly studied the structural, thermal, and electrical properties of the [(1−x)PEO: xTMSN] blend for utilizing it as a matrix, where x = 0–0.25 in mole fraction. The FT-IR spectra and XRD patterns of the blends exhibited PEO-alike up to x = 0.15 mole and TMSN-alike for x > 0.15 mole. Differential scanning calorimetry revealed formation of a eutectic phase from x = 0.1 mole and phase separation from x = 0.15 mole. The blends with x = 0.1–0.15 mole had a low value of PEO crystallinity. Thermogravimetric analysis showed thermal stability of the blends up to 75 °C. The blends exhibited electrical conductivity, σ25°C more than 10−9 S cm−1, and Arrhenius behavior (activation energy, ~0.8 eV) in a temperature region, 25–50 °C

Electrical Transport, Structural, Optical and Thermal Properties of [(1−x)Succinonitrile: xPEO]-LiTFSI-Co(bpy)3(TFSI)2-Co(bpy)3(TFSI)3 Solid Redox Mediators

The solar cell has been considered one of the safest modes for electricity generation. In a dye-sensitized solar cell, a commonly used iodide/triiodide redox mediator inhibits back-electron transfer reactions, regenerates dyes, and reduces triiodide into iodide. The use of iodide/triiodide redox, however, imposes several problems and hence needs to be replaced by alternative redox. This paper reports the first Co2+/Co3+ solid redox mediators, prepared using [(1−x)succinonitrile: xPEO] as a matrix and LiTFSI, Co(bpy)3(TFSI)2, and Co(bpy)3(TFSI)3 as sources of ions. The electrolytes are referred to as SN_E (x = 0), Blend 1_E (x = 0.5 with the ethereal oxygen of the PEO-to-lithium ion molar ratio (EO/Li+) of 113), Blend 2_E (x = 0.5; EO/Li+ = 226), and PEO_E (x = 1; EO/Li+ = 226), which achieved electrical conductivity of 2.1 × 10−3, 4.3 × 10−4, 7.2 × 10−4, and 9.7 × 10−7 S cm−1, respectively at 25 °C. Only the blend-based polymer electrolytes exhibited the Vogel-Tamman-Fulcher-type behavior (vitreous nature) with a required low pseudo-activation energy (0.05 eV), thermal stability up to 125 °C, and transparency in UV-A, visible, and near-infrared regions. FT-IR spectroscopy demonstrated the interaction between salt and matrix in the following order: SN_E < Blend 2_E < Blend 1_E << PEO_E. The results were compared with those of acetonitrile-based liquid electrolyte, ACN_E

Reducing Amplified Spontaneous Emission Threshold in CsPbBr3 Quantum Dot Films by Controlling TiO2 Compact Layer

Amplified spontaneous emission (ASE) threshold in CsPbBr3 quantum dot films is systematically reduced by introducing high quality TiO2 compact layer grown by atomic-layer deposition. Uniform and pinhole-free TiO2 films of thickness 10, 20 and 50 nm are used as a substrates for CsPbBr3 quantum dot films to enhance amplified spontaneous emission performance. The reduction is attributed indirectly to the improved morphology of TiO2 compact layer and subsequently CsPbBr3 active layer as grown on better quality substrates. This is quantified by the reduced roughness of the obtained films to less than 5 nm with 50 nm TiO2 substrate. Considering the used growth method for the quantum dot film, the improved substrate morphology maintains better the structure of the used quantum dots in the precursor solution. This results in better absorption and hence lower threshold of ASE. Besides that, the improved film quality results further in reducing light scattering and hence additional slight optical enhancement. The work demonstrates a potential venue to reduce the amplified spontaneous emission threshold of quantum dot films and therefore enhanced their optical performance

Synthesis of Pure Brookite Nanorods in a Nonaqueous Growth Environment

Brookite TiO2 is the most difficult TiO2 polymorph to synthesize. The available methods in the literature to produce brookite nanostructures mostly use water-based techniques for the preparation of water-soluble Ti complexes first, followed by a hydrothermal growth of the brookite nanostructures. Besides its multi-step nature, achieving a single brookite phase and optimizing the aqueous growth environment are all issues to be hardly controlled. In this work, pure brookite TiO2 nanorods are synthesized using tetrabutyl titanate Ti(OBu)4 and Sodium Fluoride (NaF) as precursor materials in a simple non-aqueous one-pot solvothermal process. Alcoholysis of only Ti(OBu)4 in ethanol resulted in pure anatase nanoparticles, while the addition of NaF was essential to promote the growth of highly pure brookite nanorods. The phase purity is confirmed by X-Ray Diffraction, Raman Spectroscopy, and High-Resolution Transmission Electron Microscopy. The growth mechanism is explained according to the Ostwald’s step rule, where Na+ ions are anticipated to have a potential role in driving the growth process towards the brookite phase