Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

CuO single crystal with exposed {001} facets--a highly efficient material for gas sensing and Li-ion battery applications.

ABSTRACT: Single crystal copper oxide nanoplatelets with a high percentage of {001} facets were synthesized by a facile hydrothermal approach. The as-prepared materials were characterized by X-ray diffraction, Fourier transform infrared spectroscopy, field emission scanning electron microscopy, and high resolution transmission microscopy. Via density functional theory calculations, it was found that the {001} facets are active crystal planes. When the single crystal CuO nanoplatelets were applied as an anode material in Li-ion batteries, they demonstrated outstanding electrochemical performance with high lithium storage capacity, satisfactory cyclability, and excellent high rate capacity. When used as a sensing material in gas sensors, they exhibited a superior sensitivity towards toxic and flammable gases.

SUBMITTER: Su D

PROVIDER: S-EPMC4148666 | biostudies-literature | 2014 Aug

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Publications

CuO single crystal with exposed {001} facets--a highly efficient material for gas sensing and Li-ion battery applications.

Su Dawei D Xie Xiuqiang X Dou Shixue S Wang Guoxiu G

Scientific reports 20140829

Single crystal copper oxide nanoplatelets with a high percentage of {001} facets were synthesized by a facile hydrothermal approach. The as-prepared materials were characterized by X-ray diffraction, Fourier transform infrared spectroscopy, field emission scanning electron microscopy, and high resolution transmission microscopy. Via density functional theory calculations, it was found that the {001} facets are active crystal planes. When the single crystal CuO nanoplatelets were applied as an an ...[more]

PMID: 25169039

Similar Datasets

Highly exposed {001} facets of titanium dioxide modified with reduced graphene oxide for dopamine sensing.

Project description:Titanium dioxide (TiO2) with highly exposed {001} facets was synthesized through a facile solvo-thermal method and its surface was decorated by using reduced graphene oxide (rGO) sheets. The morphology and chemical composition of the prepared rGO/TiO2 {001} nanocomposite were examined by using suitable characterization techniques. The rGO/TiO2 {001} nanocomposite was used to modify glassy carbon electrode (GCE), which showed higher electrocatalytic activity towards the oxidation of dopamine (DA) and ascorbic acid (AA), when compared to unmodified GCE. The differential pulse voltammetric studies revealed good sensitivity and selectivity nature of the rGO/TiO2 {001} nanocomposite modified GCE for the detection of DA in the presence of AA. The modified GCE exhibited a low electrochemical detection limit of 6??M over the linear range of 2-60??M. Overall, this work provides a simple platform for the development of GCE modified with rGO/TiO2 {001} nanocomposite with highly exposed {001} facets for potential electrochemical sensing applications.

| S-EPMC4031468 | biostudies-literature

Anatase TiO2 Nanoparticles with Exposed {001} Facets for Efficient Dye-Sensitized Solar Cells.

Project description:Anatase TiO2 nanoparticles with exposed {001} facets were synthesized from Ti powder via a sequential hydrothermal reaction process. At the first-step hydrothermal reaction, H-titanate nanowires were obtained in NaOH solution with Ti powder, and at second-step hydrothermal reaction, anatase TiO2 nanoparticles with exposed {001} facets were formed in NH4F solution. If the second-step hydrothermal reaction was carried out in pure water, the H-titanate nanowires were decomposed into random shape anatase-TiO2 nanostructures, as well as few impurity of H2Ti8O17 phase and rutile TiO2 phase. Then, the as-prepared TiO2 nanostructures synthesized in NH4F solution and pure water were applied to the photoanodes of dye-sensitized solar cells (DSSCs), which exhibited power conversion efficiency (PCE) of 7.06% (VOC of 0.756 V, JSC of 14.80 mA/cm(2), FF of 0.631) and 3.47% (VOC of 0.764 V, JSC of 6.86 mA/cm(2), FF of 0.662), respectively. The outstanding performance of DSSCs based on anatase TiO2 nanoparticles with exposed {001} facets was attributed to the high activity and large special surface area for excellent capacity of dye adsorption.

| S-EPMC4507182 | biostudies-literature

Defective titanium dioxide single crystals exposed by high-energy {001} facets for efficient oxygen reduction.

Project description:The cathodic material plays an essential role in oxygen reduction reaction for energy conversion and storage systems. Titanium dioxide, as a semiconductor material, is usually not recognized as an efficient oxygen reduction electrocatalyst owning to its low conductivity and poor reactivity. Here we demonstrate that nano-structured titanium dioxide, self-doped by oxygen vacancies and selectively exposed with the high-energy {001} facets, exhibits a surprisingly competitive oxygen reduction activity, excellent durability and superior tolerance to methanol. Combining the electrochemical tests with density-functional calculations, we elucidate the defect-centred oxygen reduction reaction mechanism for the superiority of the reductive {001}-TiO2-x nanocrystals. Our findings may provide an opportunity to develop a simple, efficient, cost-effective and promising catalyst for oxygen reduction reaction in energy conversion and storage technologies.

| S-EPMC4846326 | biostudies-literature

CuO-Ga2O3 Thin Films as a Gas-Sensitive Material for Acetone Detection.

Project description:The p-n heterostructures of CuO-Ga2O3 obtained by magnetron sputtering technology in a fully reactive mode (deposition in pure oxygen) were tested under exposure to low acetone concentrations. After deposition, the films were annealed at previously confirmed conditions (400 °C/4 h/synthetic air) and further investigated by utilization of X-ray diffraction (XRD), X-ray reflectivity (XRR), energy-dispersive X-ray spectroscopy (EDS). The gas-sensing behavior was tested in the air/acetone atmosphere in the range of 0.1-1.25 ppm, as well as at various relative humidity (RH) levels (10-85%). The highest responses were obtained for samples based on the CuO-Ga2O3 (4% at. Ga).

| S-EPMC7309060 | biostudies-literature

A Chelation Strategy for In-situ Constructing Surface Oxygen Vacancy on {001} Facets Exposed BiOBr Nanosheets.

Project description:Surface defect of nanomaterials is an important physical parameter which significantly influences their physical and chemical performances. In this work, high concentration of surface oxygen vancancies (SOVs) are successfully introduced on {001} facets exposed BiOBr nanosheets via a simple surface modification using polybasic carboxylic acids. The chelation interaction between carboxylic acid anions and Bi(3+) results in the weakness of Bi-O bond of BiOBr. Afterwards, under visible-light irradiation, the oxygen atoms would absorb the photo-energy and then be released from the surface of BiOBr, leaving SOVs. The electron spin resonance (ESR), high-resolution transmission electron microscopy (HRTEM), and UV-vis diffuse reflectance spectra (DRS) measurements confirm the existence of SOVs. The SOVs can enhance the absorption in visible light region and improve the separation efficiency of photo-generated charges. Hence, the transformation rate of adsorbed O2 on the as-prepared BiOBr with SOVs to superoxide anion radicals (•O2(-)) and the photocatalytic activity are greatly enhanced. Based on the modification by several carboxylic acids and the photocatalytic results, we propose that carboxylic acids with natural bond orbital (NBO) electrostatic charges absolute values greater than 0.830 are effective in modifying BiOBr.

| S-EPMC4845065 | biostudies-literature

A porous 3D-RGO@MWCNT hybrid material as Li-S battery cathode.

Project description:In this work, a unique three-dimensional (3D) structured carbon-based composite was synthesized. In the composite, multiwalled carbon nanotubes (MWCNT) form a lattice matrix in which porous spherical reduced graphene oxide (RGO) completes the 3D structure. When used in Li-S batteries, the 3D porous lattice matrix not only accommodates a high content of sulfur, but also induces a confinement effect towards polysulfide, and thereby reduces the "shuttle effect". The as-prepared S-3D-RGO@MWCNT composite delivers an initial specific capacity of 1102 mAh·g-1. After 200 charging/discharge cycles, a capacity of 805 mAh·g-1 and a coulombic efficiency of 98% were maintained, implying the shuttle effect was greatly suppressed by the composite matrix. In addition, the S-3D-RGO@MWCNT composite also exhibits an excellent rate capability.

| S-EPMC6404391 | biostudies-literature

Reaction temperature sensing (RTS)-based control for Li-ion battery safety.

Project description:We report reaction temperature sensing (RTS)-based control to fundamentally enhance Li-ion battery safety. RTS placed at the electrochemical interface inside a Li-ion cell is shown to detect temperature rise much faster and more accurately than external measurement of cell surface temperature. We demonstrate, for the first time, that RTS-based control shuts down a dangerous short-circuit event 3 times earlier than surface temperature- based control and prevents cell overheating by 50 °C and the resultant cell damage.

| S-EPMC4675999 | biostudies-literature

Enhanced Photocatalysis from Truncated Octahedral Bipyramids of Anatase TiO<sub>2</sub> with Exposed {001}/{101} Facets.

Project description:In this study, we develop a new synthetic method to grow anatase TiO2 crystals composed of truncated octahedral bipyramids (TOBs) with exposed {001} and {101} facets by a vapor-solid reaction growth (VSRG) method. The VSRG method employs TiCl4(g) to react with CaO(s)/Ca(OH)2(s) at 823-1043 K under atmospheric pressure. The O-deficient pale-blue TOB TiO2 crystals display high amount of both {001} and {101} facets. Together, they decompose methylene blue photocatalytically under UV-visible (UV-vis) light irradiation. The most-efficient TOB catalyst VT923 (grown at 923 K, average edge length 400 nm, average thickness 200 nm, and surface area 4.20 m2/g) shows a degradation rate constant k, 0.0527 min-1. This is close to that of the P25 standard 0.0577 min-1. However, the surface area of P25 (46.8 m2/g) is about 12 times that of VT923. The extraordinary performance of VT923 is attributed to the presence of high amount of coexisting {001} and {101} facets to form effective surface heterojunctions. They would separate photogenerated electrons and holes effectively on {101} and {001} surfaces, respectively. For VT923, the {001}/{101} ratio is 0.764, which is close to 1, the highest value observed for all TOB samples grown in this study. The surface heterojunctions prolong the electron-hole separation so that VT923 demonstrates the excellent photocatalytic capability. In addition, residual Cl atoms on the exposed faces are easily removed to show clean TiO surface layers with sufficient amount of O-deficient sites in the current samples.

| S-EPMC6644679 | biostudies-literature

Yucca fern shaped CuO nanowires on Cu foam for remitting capacity fading of Li-ion battery anodes.

Project description:To remit capacity fading of lithium ion battery (LIB) anodes, freestanding yucca fern shaped CuO nanowires (NWs) on Cu foams are fabricated as anodes by combining facile and scalable anodization of copper foams followed by calcination. The porous and radial configuration of the hierarchical CuO NWs on the Cu foam substrate guarantees the remarkably improved electrochemical performance with durable cycle stability and excellent rate capability compared with CuO NWs on Cu foils. The reversible capacity remains 461.5 mAh/g after 100 repeated cycles at a current density of 100 mA/g, and a capacity of 150.6 mAh/g even at a high rate of 1000 mA/g. By examining the surface morphology of the cycled samples, possible performance fading route is proposed. The 3D CuO NWs network with a porous architecture simutaneously reduces the ion diffusion distances, promotes the electrolyte permeation and electronic conductivity. This novel strategy might open a new window to develop durable CuO based composite anodes for LIBs.

| S-EPMC5916934 | biostudies-literature

True Photoreactivity Origin of Ti3+-Doped Anatase TiO2 Crystals with Respectively Dominated Exposed {001}, {101}, and {100} Facets.

Project description:Combining the advantages of reactive crystal facets and engineering defects is an encouraging way to address the inherent disadvantages of titanium dioxide (TiO2) nanocrystals. However, revealing the true photoreactivity origin for defective TiO2 with coexposed or predominant exposed anisotropic facets is still highly challenging. Here, the photoreactivity of TiO2 nanocrystals with respectively predominant exposed {001}, {101}, and {100} facets before and after Ti3+ doping under both ultraviolet and visible light was compared systematically. In detail, the photocatalytic H2 production for R-TiO2-001, R-TiO2-101, and R-TiO2-100 increased by a factor of 1.34, 2.65, and 3.39 under UV light and a factor of 8.90, 13.47, and 8.72 under visible light. By contrast, the photocatalytic degradation of methyl orange for R-TiO2-001, R-TiO2-101, and R-TiO2-100 increased by a factor of 3.18, 1.42, and 2.17 under UV light and a factor of 4.03, 2.85, and 1.58 under visible light, respectively. The true photocatalytic activity origin for the obtained photoreduction and photo-oxidation ability is attributed to the exposure of more active sites (under-coordinated 5-fold Ti atoms), the facilitated charge transfer among {001}, {101}, and {100} facets, and the Ti3+ energy state with variable doping levels to extend the visible light response. This work hopefully provides significant insights into the photoreactivity origin of defective TiO2 nanocrystals with anisotropic exposed facets.

| S-EPMC6751725 | 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