Browse
Submit Data
Databases
API
Help

Dataset Information

20 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

One-Step Solution Deposition of Antimony Selenoiodide Films via Precursor Engineering for Lead-Free Solar Cell Applications.

ABSTRACT: Ternary chalcohalides are promising lead-free photovoltaic materials with excellent optoelectronic properties. We propose a simple one-step solution-phase precursor-engineering method for antimony selenoiodide (SbSeI) film fabrication. SbSeI films were fabricated by spin-coating the precursor solution, and heating. Various precursor solutions were synthesized by adjusting the molar ratio of two solutions based on SbCl₃-selenourea and SbI₃. The results suggest that both the molar ratio and the heating temperature play key roles in film phase and morphology. Nanostructured SbSeI films with a high crystallinity were obtained at a molar ratio of 1:1.5 and a temperature of 150 °C. The proposed method could be also used to fabricate (Bi,Sb)SeI.

SUBMITTER: Choi YC

PROVIDER: S-EPMC8703622 | biostudies-literature |

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Similar Datasets

Photoexcitation dynamics in solution-processed formamidinium lead iodide perovskite thin films for solar cell applications.

Project description:Formamidinium lead iodide (FAPbI3) is a newly developed hybrid perovskite that potentially can be used in high-efficiency solution-processed solar cells. Here, the temperature-dependent dynamic optical properties of three types of FAPbI3 perovskite films (fabricated using three different precursor systems) are comparatively studied. The time-resolved photoluminescence (PL) spectra reveal that FAPbI3 films made from the new precursor (a mixture of formamidinium iodide and hydrogen lead triiodide) exhibit the longest lifetime of 439 ns at room temperature, suggesting a lower number of defects and lower non-radiative recombination losses compared with FAPbI3 obtained from the other two precursors. From the temperature-dependent PL spectra, a phase transition in the films is clearly observed. Meanwhile, exciton-binding energies of 8.1 and 18 meV for the high- and low-temperature phases are extracted, respectively. Importantly, the PL spectra for all of the samples show a single peak at room temperature, whereas at liquid-helium temperature the emission features two peaks: one in higher energy displaying a fast decay (0.5 ns) and a second red-shifted peak with a decay of up to several microseconds. These two emissions, separated by ~18 meV, are attributed to free excitons and bound excitons with singlet and triplet characters, respectively.

| S-EPMC6059954 | biostudies-literature

Controlled Growth of BiSI Nanorod-Based Films Through a Two-Step Solution Process for Solar Cell Applications.

Project description:Pb-based hybrid perovskite solar cells, despite their advantages, face challenges in commercialization. In recent years, Bi-based chalcohalides are being considered as potential alternative candidates, however, their current device efficiency remains unsatisfactory. Herein, a two-step solution method is developed and applied to the fabrication of BiSI films. The method consists of the formation of Bi2S3 (step I) and its conversion to BiSI (step II). The Bi2S3 was fabricated by a thiol-amine solution process and the BiSI conversion was achieved by chemical reaction between the as-formed Bi2S3 and BiI3. It was found that the formation of BiSI was highly dependent on the Bi:S molar ratio of the Bi2O3-thiourea solution and the number of times of step I. The as-fabricated BiSI film had an optical band gap of 1.61 eV and exhibited nanorod morphology. In addition, the electronic structure is explored and discussed for solar cells applications.

| S-EPMC6956077 | biostudies-literature

Fabrication of Lead-Free Bi0.5Na0.5TiO₃ Thin Films by Aqueous Chemical Solution Deposition.

Project description:Piezoelectric ceramics are widely used in actuator applications, and currently the vast majority of these devices are based on Pb ( Zr , Ti ) O 3 , which constitutes environmental and health hazards due to the toxicity of lead. One of the most promising lead-free material systems for actuators is based on Bi 0 . 5 Na 0 . 5 TiO 3 (BNT), and here we report on successful fabrication of BNT thin films by aqueous chemical solution deposition. The precursor solution used in the synthesis is based on bismuth citrate stabilized by ethanolamine, NaOH , and a Ti-citrate prepared from titanium tetraisopropoxide and citric acid. BNT thin films were deposited on SrTiO 3 and platinized silicon substrates by spin-coating, and the films were pyrolized and annealed by rapid thermal processing. The BNT perovskite phase formed after calcination at 500 °C in air. The deposited thin films were single phase according to X-ray diffraction, and the microstructures of the films shown by electron microscopy were homogeneous and dense. Decomposition of the gel was thoroughly investigated, and the conditions resulting in phase pure materials were identified. This new aqueous deposition route is low cost, robust, and suitable for development of BNT based thin film for actuator applications.

| S-EPMC5459111 | biostudies-other

Radio Frequency Magnetron Sputtering Deposition of TiO2 Thin Films and Their Perovskite Solar Cell Applications.

Project description:In this work, we report a physical deposition based, compact (cp) layer synthesis for planar heterojunction perovskite solar cells. Typical solution-based synthesis of cp layer for perovskite solar cells involves low-quality of thin films, high-temperature annealing, non-flexible devices, limitation of large-scale production and that the effects of the cp layer on carrier transport have not been fully understood. In this research, using radio frequency magnetron sputtering (RFMS), TiO2 cp layers were fabricated and the thickness could be controlled by deposition time; CH3NH3PbI3 films were prepared by evaporation &immersion (E &I) method, in which PbI2 films made by thermal evaporation technique were immersed in CH3NH3I solution. The devices exhibit power conversion efficiency (PCE) of 12.1% and the photovoltaic performance can maintain 77% of its initial PCE after 1440 h. The method developed in this study has the capability of fabricating large active area devices (40 × 40 mm(2)) showing a promising PCE of 4.8%. Low temperature and flexible devices were realized and a PCE of 8.9% was obtained on the PET/ITO substrates. These approaches could be used in thin film based solar cells which require high-quality films leading to reduced fabrication cost and improved device performance.

| S-EPMC4668551 | biostudies-literature

Solar Cell Applications of Solution-Processed AgInGaSe2 Thin Films and Improved Properties by Sodium Doping.

Project description:Binary nanoparticle inks comprising Ag2Se, In2Se3, and Ga2Se3 were fabricated via a wet ball-milling method and were further used to fabricate AgInGaSe2 (AIGS) precursors by sequentially spraying the inks onto a Mo-coated substrate. AIGS precursors were annealed under a Se atmosphere for 1 h at 570 °C. Na2Se thin layers of varying thicknesses (0, 5, 10, and 20 nm) were vacuum-evaporated onto the Mo layer prior to the AIGS precursors being fabricated to investigate the influence on AIGS solar cells. Sodium plays a critical role in improving the material properties and performance of AIGS thin-film solar cells. The grain size of the AIGS films was significantly improved by sodium doping. Secondary ion mass spectroscopy illustrated slight surficial sodium segregation and heavy sodium segregation at the AIGS/Mo interface. Double-graded band profiles were observed in the AIGS films. With the increase in Na2Se thickness, the basic photovoltaic characteristics of the AIGS solar cells were significantly improved. The highest solar cell conversion efficiency of 6.6% (open-circuit voltage: 775.6 mV, short-circuit current: 15.5 mA/cm2, fill factor: 54.9%, area: 0.2 cm2) was obtained when the Na2Se thickness was 20 nm.

| S-EPMC7153622 | biostudies-literature

Atomic Layer Deposition of Titanium Oxide-Based Films for Semiconductor Applications—Effects of Precursor and Operating Conditions

Project description:Two widely used atomic layer deposition precursors, Tetrakis (dimethylamido) titanium (TDMA-Ti) and titanium tetrachloride (TiCl4), were investigated for use in the deposition of TiOx-based thin films as a passivating contact material for solar cells. This study revealed that both precursors are suited to similar deposition temperatures (150 °C). Post-deposition annealing plays a major role in optimising the titanium oxide (TiOx) film passivation properties, improving minority carrier lifetime (τeff) by more than 200 µs. Aluminium oxide deposited together with titanium oxide (AlOy/TiOx) reduced the sheet resistance by 40% compared with pure TiOx. It was also revealed that the passivation quality of the (AlOy/TiOx) stack depends on the precursor and ratio of AlOy to TiOx deposition cycles.

| S-EPMC10456286 | biostudies-literature

Quantification of light-enhanced ionic transport in lead iodide perovskite thin films and its solar cell applications.

Project description:Ionic transport in organometal halide perovskites is of vital importance because it dominates anomalous phenomena in perovskite solar cells, from hysteresis to switchable photovoltaic effects. However, excited state ionic transport under illumination has remained elusive, although it is essential for understanding the unusual light-induced effects (light-induced self-poling, photo-induced halide segregation and slow photoconductivity response) in organometal halide perovskites for optoelectronic applications. Here, we quantitatively demonstrate light-enhanced ionic transport in CH3NH3PbI3 over a wide temperature range of 17-295 K, which reveals a reduction in ionic transport activation energy by approximately a factor of five (from 0.82 to 0.15 eV) under illumination. The pure ionic conductance is obtained by separating it from the electronic contribution in cryogenic galvanostatic and voltage-current measurements. On the basis of these findings, we design a novel light-assisted method of catalyzing ionic interdiffusion between CH3NH3I and PbI2 stacking layers in sequential deposition perovskite synthesis. X-ray diffraction patterns indicate a significant reduction of PbI2 residue in the optimized CH3NH3PbI3 thin film produced via light-assisted sequential deposition, and the resulting solar cell efficiency is increased by over 100% (7.5%-15.7%) with little PbI2 residue. This new method enables fine control of the reaction depth in perovskite synthesis and, in turn, supports light-enhanced ionic transport.

| S-EPMC6062189 | biostudies-literature

Vapor transport deposition of antimony selenide thin film solar cells with 7.6% efficiency.

Project description:Antimony selenide is an emerging promising thin film photovoltaic material thanks to its binary composition, suitable bandgap, high absorption coefficient, inert grain boundaries and earth-abundant constituents. However, current devices produced from rapid thermal evaporation strategy suffer from low-quality film and unsatisfactory performance. Herein, we develop a vapor transport deposition technique to fabricate antimony selenide films, a technique that enables continuous and low-cost manufacturing of cadmium telluride solar cells. We improve the crystallinity of antimony selenide films and then successfully produce superstrate cadmium sulfide/antimony selenide solar cells with a certified power conversion efficiency of 7.6%, a net 2% improvement over previous 5.6% record of the same device configuration. We analyze the deep defects in antimony selenide solar cells, and find that the density of the dominant deep defects is reduced by one order of magnitude using vapor transport deposition process.

| S-EPMC5988661 | biostudies-literature

Surface engineering of perovskite films for efficient solar cells.

Project description:It is critical to prepare smooth and dense perovskite films for the fabrication of high efficiency perovskite solar cells. However, solution casting process often results in films with pinhole formation and incomplete surface coverage. Herein, we demonstrate a fast and efficient vacuum deposition method to optimize the surface morphology of solution-based perovskite films. The obtained planar devices exhibit an average power conversion efficiency (PCE) of 13.42% with a standard deviation of ±2.15% and best efficiency of 15.57%. Furthermore, the devices also show excellent stability of over 30 days with a slight degradation <9% when stored under ambient conditions. We also investigated the effect of vacuum deposition thickness on the electron transportation and overall performance of the devices. This work provides a versatile approach to prepare high-quality perovskite films and paves a way for high-performance and stable perovskite photovoltaic devices.

| S-EPMC5670249 | biostudies-literature

Reactive Inorganic Vapor Deposition of Perovskite Oxynitride Films for Solar Energy Conversion.

Project description:The synthesis of perovskite oxynitrides, which are promising photoanode candidates for solar energy conversion, is normally accomplished by high-temperature ammonolysis of oxides and carbonate precursors, thus making the deposition of their planar films onto conductive substrates challenging. Here, we proposed a facile strategy to prepare a series of perovskite oxynitride films. Taking SrTaO2N as a prototype, we prepared SrTaO2N films on Ta foils under NH3 flow by utilizing the vaporized SrCl2/SrCO3 eutectic salt. The SrTaO2N films exhibit solar water-splitting photocurrents of 3.0 mA cm-2 at 1.23 V vs. RHE (reversible hydrogen electrode), which increases by 270% compared to the highest photocurrent (1.1 mA cm-2 at 1.23 V vs. RHE) of SrTaO2N reported in the literature. This strategy may also be applied to directly prepare a series of perovskite oxynitride films on conductive substrates such as ATaO2N (A = Ca, Ba) and ANbO2N (A = Sr, Ba).

| S-EPMC6946269 | biostudies-literature

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data