Browse
Submit Data
Databases
API
Help

Dataset Information

32 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Crystallinity Engineering of Hematite Nanorods for High-Efficiency Photoelectrochemical Water Splitting.

ABSTRACT: An effective strategy to overcome the morphology evolution of hematite nanorods under high-temperature activation is presented, via tuning the crystallinity and sintering temperature by substrate modification. It is demonstrated that the as-prepared doping-free hematite nanorods with fine nanostructures obtain a significantly higher photocurrent density of 2.12 mA cm-2 at 1.23 V versus RHE, due to effective charge separation and transfer.

SUBMITTER: Wang D

PROVIDER: S-EPMC5016786 | biostudies-literature | 2015 Apr

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Publications

Crystallinity Engineering of Hematite Nanorods for High-Efficiency Photoelectrochemical Water Splitting.

Wang Degao D Zhang Yuying Y Peng Cheng C Wang Jianqiang J Huang Qing Q Su Shao S Wang Lianhui L Huang Wei W Fan Chunhai C

Advanced science (Weinheim, Baden-Wurttemberg, Germany) 20150316 4

An effective strategy to overcome the morphology evolution of hematite nanorods under high-temperature activation is presented, via tuning the crystallinity and sintering temperature by substrate modification. It is demonstrated that the as-prepared doping-free hematite nanorods with fine nanostructures obtain a significantly higher photocurrent density of 2.12 mA cm-2 at 1.23 V versus RHE, due to effective charge separation and transfer. ...[more]

PMID: 27660739

Similar Datasets

Efficiency limits for photoelectrochemical water-splitting.

Project description:Theoretical limiting efficiencies have a critical role in determining technological viability and expectations for device prototypes, as evidenced by the photovoltaics community's focus on detailed balance. However, due to their multicomponent nature, photoelectrochemical devices do not have an equivalent analogue to detailed balance, and reported theoretical efficiency limits vary depending on the assumptions made. Here we introduce a unified framework for photoelectrochemical device performance through which all previous limiting efficiencies can be understood and contextualized. Ideal and experimentally realistic limiting efficiencies are presented, and then generalized using five representative parameters-semiconductor absorption fraction, external radiative efficiency, series resistance, shunt resistance and catalytic exchange current density-to account for imperfect light absorption, charge transport and catalysis. Finally, we discuss the origin of deviations between the limits discussed herein and reported water-splitting efficiencies. This analysis provides insight into the primary factors that determine device performance and a powerful handle to improve device efficiency.

| S-EPMC5146289 | biostudies-literature

Surface engineered doping of hematite nanorod arrays for improved photoelectrochemical water splitting.

Project description:Given the narrow band gap enabling excellent optical absorption, increased charge carrier density and accelerated surface oxidation reaction kinetics become the key points for improved photoelectrochemical performances for water splitting over hematite (α-Fe2O3) photoanodes. In this study, a facile and inexpensive method was demonstrated to develop core/shell structured α-Fe2O3 nanorod arrays. A thin, Ag-doped overlayer of ~2-3 nm thickness was formed along α-Fe2O3 nanorods via ultrasonication treatment of solution-based β-FeOOH nanorods in Ag precursor solution followed by high temperature annealing. The obtained α-Fe2O3/AgxFe2-xO3 core/shell nanorod films demonstrated much higher photoelectrochemical performances as photoanodes than the pristine α-Fe2O3 nanorod film, especially in the visible light region; the incident photon-to-current efficiency (IPCE) at 400 nm was increased from 2.2% to 8.4% at 1.23 V vs. RHE (Reversible hydrogen electrode). Mott-Schottky analysis and X-ray absorption spectra revealed that the Ag-doped overlayer not only increased the carrier density in the near-surface region but also accelerated the surface oxidation reaction kinetics, synergistically contributing to the improved photoelectrochemical performances. These findings provide guidance for the design and optimization of nanostructured photoelectrodes for efficient solar water splitting.

| S-EPMC4197419 | biostudies-literature

Controlled fabrication of Sn/TiO2 nanorods for photoelectrochemical water splitting.

Project description:In this work, we investigate the controlled fabrication of Sn-doped TiO2 nanorods (Sn/TiO2 NRs) for photoelectrochemical water splitting. Sn is incorporated into the rutile TiO2 nanorods with Sn/Ti molar ratios ranging from 0% to 3% by a simple solvothermal synthesis method. The obtained Sn/TiO2 NRs are single crystalline with a rutile structure. The concentration of Sn in the final nanorods can be well controlled by adjusting the molar ratio of the precursors. Photoelectrochemical experiments are conducted to explore the photocatalytic activity of Sn/TiO2 NRs with different doping levels. Under the illumination of solar simulator with the light intensity of 100 mW/cm2, our measurements reveal that the photocurrent increases with increasing doping level and reaches the maximum value of 1.01 mA/cm2 at -0.4 V versus Ag/AgCl, which corresponds to up to about 50% enhancement compared with the pristine TiO2 NRs. The Mott-Schottky plots indicate that incorporation of Sn into TiO2 nanorod can significantly increase the charge carrier density, leading to enhanced conductivity of the nanorod. Furthermore, we demonstrate that Sn/TiO2 NRs can be a promising candidate for photoanode in photoelectrochemical water splitting because of their excellent chemical stability.

| S-EPMC4228341 | biostudies-literature

Origin of High-Efficiency Photoelectrochemical Water Splitting on Hematite/Functional Nanohybrid Metal Oxide Overlayer Photoanode after a Low Temperature Inert Gas Annealing Treatment.

Project description:A simplistic and low-cost method that dramatically improves the performance of solution-grown hematite photoanodes for solar-driven water splitting through incorporation of nanohybrid metal oxide overlayers was developed. By heating the α-Fe2O3/SnO2-TiO2 electrode in an inert atmosphere, such as argon or nitrogen, the photocurrent increased to over 2 mA/cm2 at 1.23 V versus a reversible hydrogen electrode, which is 10 times higher than that of pure hematite under 1 sun (100 mW/cm2, AM 1.5G) light illumination. For the first time, we found a significant morphological difference between argon and nitrogen gas heat-treated hematite films and discussed the consequences for photoresponse. The origin for the enhancement, probed via theoretical modeling, stems from the facile incorporation of low formation energy dopants into the Fe2O3 layer at the interface of the metal oxide nanohybrid overlayer, which decreases recombination by increasing the electrical conductivity of Fe2O3. These dopants diffuse from the overlayer into the α-Fe2O3 layer readily under inert gas heat treatment. This simple yet effective strategy could be applied to other dopants to increase hematite performance for solar energy conversion applications.

| S-EPMC6649254 | biostudies-literature

Band gap and Morphology Engineering of Hematite Nanoflakes from an Ex Situ Sn Doping for Enhanced Photoelectrochemical Water Splitting.

Project description:In this article, we report a simple ex situ Sn-doping method on hematite nanoflakes (coded as MSnO2-H) that can protect the nanoflake (NF) morphology against the 800 °C high-temperature annealing process and activate the photoresponse of hematite until 800 nm wavelength excitation. MSnO2-H has been fabricated by dropping SnCl4 ethanol solution on hematite nanoflakes homogeneously grown over the conductive FTO glass substrate and annealed at 500 °C to synthesize the SnO2 nanoparticles on hematite NFs. The Sn-treated samples were then placed in a furnace again, and the sintering process was conducted at 800 °C for 15 min. During this step, structure deformation of hematite occurs normally due to the grain boundary motion and oriented attachment. However, in the case of MSnO2-H, the outer SnO2 nanoparticles efficiently prevented a shape deformation and maintained the nanoflake shape owing to the encapsulation of hematite NFs. Furthermore, the interface of hematite/SnO2 nanoparticles became the spots for a heavy Sn ion doping. We demonstrated the generation of the newly localized states, resulting in an extension of the photoresponse of hematite until 800 nm wavelength light irradiation. Furthermore, we demonstrated that SnO2 nanoparticles can effectively act as a passivation layer, which can reduce the onset potential of hematite for water splitting redox reactions. The optimized MSnO2-H nanostructures showed a 2.84 times higher photocurrent density and 300 mV reduced onset potential compared with a pristine hematite nanoflake photoanode.

| S-EPMC9535642 | biostudies-literature

High-throughput parallel testing of ten photoelectrochemical cells for water splitting: case study on the effects of temperature in hematite photoanodes.

Project description:High-throughput testing of photoelectrochemical cells and materials under well-defined operating conditions can accelerate the discovery of new semiconducting materials, the characterization of the phenomena occurring at the semiconductor-electrolyte interface, or the understanding of the coupled multi-physics transport phenomena of a complete working cell. However, there have been few high-throughput systems capable of dealing with complete cells and applying variations in real-life operating conditions, like temperature or irradiance. Understanding the effects of the variations of these real-life operating conditions on the performance of photoelectrode materials requires reliable and reproducible measurements. In this work, we report on a setup that simultaneously tests ten individual, identical photoelectrochemical cells whilst controlling temperature. The effects of temperature from 26 to 65 °C were studied in tin-doped hematite photoanodes for water splitting - as a reference case - through cyclic voltammetry and electrochemical impedance spectroscopy. The increase of surface-state-mediated charge recombination with temperature mainly penalized the energy conversion efficiency due to the reduction of the photovoltage produced. For parallel measurements in the ten individual cells, standard deviations from 20 to 60 mV for the onset potentials and less than 0.2 mA cm-2 for saturation current densities quantified the reproducibility of the results.

| S-EPMC11302243 | biostudies-literature

Enhancing photoelectrochemical water splitting by combining work function tuning and heterojunction engineering.

Project description:We herein demonstrate the unusual effectiveness of two strategies in combination to enhance photoelectrochemical water splitting. First, the work function adjustment via molybdenum (Mo) doping significantly reduces the interfacial energy loss and increases the open-circuit photovoltage of bismuth vanadate (BiVO4) photoelectrochemical cells. Second, the creation and optimization of the heterojunction of boron (B) doping carbon nitride (C3N4) and Mo doping BiVO4 to enforce directional charge transfer, accomplished by work function adjustment via B doping for C3N4, substantially boost the charge separation of photo-generated electron-hole pairs at the B-C3N4 and Mo-BiVO4 interface. The synergy between the above efforts have significantly reduced the onset potential, and enhanced charge separation and optical properties of the BiVO4-based photoanode, culminating in achieving a record applied bias photon-to-current efficiency of 2.67% at 0.54 V vs. the reversible hydrogen electrode. This work sheds light on designing and fabricating the semiconductor structures for the next-generation photoelectrodes.

| S-EPMC6695449 | biostudies-literature

Effects of Anions and pH on the Stability of ZnO Nanorods for Photoelectrochemical Water Splitting.

Project description:This work demonstrates the improved stability of zinc oxide nanorods (ZnO NRs) for the photoanode of solar water splitting under voltage biases by the addition of borate or carbonate ions in the aqueous electrolyte with suitable pH ranges. The ZnO NRs prepared by the hydrothermal method are highly active and stable at pH 10.5 in both borate and carbonate buffer solutions, where a photocurrent higher than 99% of the initial value has been preserved after 1 h polarization at 1.5 V (vs reversible hydrogen electrode) under AM 1.5G. The optimal pH ranges with a minimum morphological change of ZnO NRs for photoelectrochemical (PEC) water splitting in borate and carbonate buffer solutions are 9-13 and 10-12, respectively. The working pH range for PEC water splitting on ZnO NR photoanodes can be extended to 8.5-12.5 by the combination of borate and carbonate anions. The lifetime of ZnO NR photoanodes can be synergistically prolonged for over an order of magnitude when the electrolyte is the binary electrolyte consisting of borate and carbonate in comparison with these two anions used individually. On the basis of the experimental results, a possible mechanism for the protective behavior of ZnO in borate and carbonate solutions is proposed. These findings can be used to improve the lifetime of other high-performance ZnO-based catalysts and to understand the photocorrosive and protective behaviors of ZnO NRs in the borate and carbonate solutions.

| S-EPMC6641385 | biostudies-literature

Tuning of oxygen vacancy-induced electrical conductivity in Ti-doped hematite films and its impact on photoelectrochemical water splitting.

Project description:Titanium (Ti)-doped hematite (α-Fe2O3) films were grown in oxygen-depleted condition by using the spray pyrolysis technique. The impact of post-deposition annealing in oxygen-rich condition on both the conductivity and water splitting efficiency was investigated. The X-ray diffraction pattern revealed that the films are of rhombohedral α-Fe2O3 structure and dominantly directed along (012). The as-grown films were found to be highly conductive with electrons as the majority charge carriers (n-type), a carrier concentration of 1.09×1020 cm-3, and a resistivity of 5.9×10-2 Ω-cm. The conductivity of the films were reduced upon post-deposition annealing. The origin of the conductivity was attributed firstly to Ti4+ substituting Fe3+ and secondly to the ionized oxygen vacancies (VO) in the crystal lattice of hematite. Upon annealing the samples in oxygen-rich condition, VO slowly depleted and the conductivity reduced. The photocurrent of the as-grown samples was found to be 3.4 mA/cm-2 at 1.23 V vs. RHE. The solar-to-hydrogen efficiency for the as-grown sample was calculated to be 4.18% at 1.23 V vs. RHE. The photocurrents were found to be significantly stable in aqueous environment. A linear relationship between conductivity and water-splitting efficiency was established.

| S-EPMC7198511 | biostudies-literature

Unassisted photoelectrochemical water splitting exceeding 7% solar-to-hydrogen conversion efficiency using photon recycling.

Project description:Various tandem cell configurations have been reported for highly efficient and spontaneous hydrogen production from photoelectrochemical solar water splitting. However, there is a contradiction between two main requirements of a front photoelectrode in a tandem cell configuration, namely, high transparency and high photocurrent density. Here we demonstrate a simple yet highly effective method to overcome this contradiction by incorporating a hybrid conductive distributed Bragg reflector on the back side of the transparent conducting substrate for the front photoelectrochemical electrode, which functions as both an optical filter and a conductive counter-electrode of the rear dye-sensitized solar cell. The hybrid conductive distributed Bragg reflectors were designed to be transparent to the long-wavelength part of the incident solar spectrum (?>500?nm) for the rear solar cell, while reflecting the short-wavelength photons (?<500?nm) which can then be absorbed by the front photoelectrochemical electrode for enhanced photocurrent generation.

| S-EPMC5476685 | 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