Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Li(3)Al(MoO(2))(2)O(2)(AsO(4))(2).

ABSTRACT: Single crystals of trilithium(I) aluminium(III) bis-[dioxidomolybdenum(VI)] dioxide bis-[arsenate(V)], Li(3)AlMo(2)As(2)O(14), have been prepared by solid-state reaction at 788?K. The structure consists of AsO(4) tetra-hedra, AlO(6) octa-hedra and Mo(2)O(10) groups sharing corners to form a three-dimensional framework containing channels running respectively along the [100] and [010] directions, where the Li(+) ions are located. This structure is compared with compounds having (MX(2)O(12))(n) chains (M = Mo, Al and X = P, As) and others containing M(2)O(10) (M = Mo, Fe) dimers.

SUBMITTER: Hajji M

PROVIDER: S-EPMC2968439 | biostudies-literature | 2009 Feb

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Publications

Li(3)Al(MoO(2))(2)O(2)(AsO(4))(2).

Hajji Mounir M Zid Mohamed Faouzi MF Driss Ahmed A

Acta crystallographica. Section E, Structure reports online 20090225 Pt 3

Single crystals of trilithium(I) aluminium(III) bis-[dioxidomolybdenum(VI)] dioxide bis-[arsenate(V)], Li(3)AlMo(2)As(2)O(14), have been prepared by solid-state reaction at 788 K. The structure consists of AsO(4) tetra-hedra, AlO(6) octa-hedra and Mo(2)O(10) groups sharing corners to form a three-dimensional framework containing channels running respectively along the [100] and [010] directions, where the Li(+) ions are located. This structure is compared with compounds having (MX(2)O(12))(n) ch ...[more]

PMID: 21582037

Similar Datasets

Na(3)Al(AsO(4))(2).

Project description:The structure of the title compound tris-odium aluminium bis-(arsenate), Na(3)Al(AsO(4))(2), is built up from AlO(4) and AsO(4) corner-sharing tetra-hedra, forming an undulating two-dimensional framework parallel to (100). The layers are constituted of large Al(6)As(6)O(36) rings made up from six AlO(4) and AsO(4) tetra-hedra in which two sodium cations are situated, the third sodium cation being located in the inter-layer space. The structural relationships between the title compound and Na(3)Fe(PO(4))(2), NaAlCo(PO(4))(2) and Al(5)Co(3)(PO(4))(8) are discussed.

| S-EPMC3569176 | biostudies-literature

The aluminoarsenate K(1.8)Sr(0.6)Al(3)(AsO(4))(4).

Project description:The title compound, potassium strontium trialuminium tetra-arsenate, was prepared by solid-state reaction. The structure consists of AlO(6) octa-hedra (site symmetries 2.. and 2/m) and two AsO(4) tetra-hedra (.2. and m..) sharing corners and edges to form a two-dimensional structure parallel to (010). The cations are occupationally disordered and are located in the interlayer space. For both types of cations, distorted coordination polyhedra are observed.

| S-EPMC3344283 | biostudies-literature

Lithium europium(III) molybdate(VI), Li(3.5)Eu(1.5)(MoO(4))(4).

Project description:The title compound, Li(3.5)Eu(1.5)(MoO(4))(4), was prepared by solid-state reactions. The fundamental building units of the structure are LiO(4) polyhedra (site symmetry [Formula: see text]), distorted LiO(6) polyhedra and MoO(4) tetra-hedra, which are further inter-connected via corner-sharing O atoms. One site is occupied by both Li and Eu atoms in a substituent disordered manner (0.25:0.75), and the Li/Eu atoms are coordinated by eight O atoms in a distorted square-antiprismatic manner.

| S-EPMC3274837 | biostudies-literature

Crystal Growth and Spectroscopic Investigations of Tm3+:Li₃Ba₂Gd₃(MoO₄)₈ Crystal.

Project description:Tm3+:Li₃Ba₂Gd₃(MoO₄)₈ crystal has been grown by the top seeded solution growth (TSSG) method from a Li₂MoO₄ flux. The room temperature polarized absorption spectra, fluorescence spectra, and fluorescence decay curves of the crystal were measured. Based on the Judd-Ofelt (J-O) theory, the main spectroscopic parameters of the crystal, including the spontaneous emission probabilities, fluorescence branching ratios, and radiative lifetimes were calculated and analyzed. The broad and strong absorption bands of the crystal show that it can be efficiently pumped by the diode laser, while the large emission cross-sections of the ³F₄ → ³H₆ transition indicate that the crystal is a promising candidate for tunable and short pulse lasers.

| S-EPMC5453121 | biostudies-other

Improved Electrochemical Performance of Li-Rich Cathode Materials via Spinel Li2MoO4 Coating.

Project description:Li-rich manganese-based cathode materials (LRMs) are considered one of the most promising cathode materials for the next generation of lithium-ion batteries (LIBs) because of their high energy density. However, there are problems such as a capacity decay, poor rate performance, and continuous voltage drop, which seriously limit their large-scale commercial applications. In this work, Li1.2Mn0.54Co0.13Ni0.13O2 coated with Li2MoO4 with a unique spinel structure was prepared with the wet chemistry method and the subsequent calcination process. The Li2MoO4 coating layer with a spinel structure could provide a 3D Li+ transport channel, which is beneficial for improving rate performance, while protecting LRMs from electrolyte corrosion, suppressing interface side reactions, and improving cycling stability. The capacity retention rate of LRMs coated with 3 wt% Li2MoO4 increased from 69.25% to 81.85% after 100 cycles at 1 C, and the voltage attenuation decreased from 7.06 to 4.98 mV per cycle. The lower Rct also exhibited an improved rate performance. The results indicate that the Li2MoO4 coating effectively improves the cyclic stability and electrochemical performance of LRMs.

| S-EPMC10456268 | biostudies-literature

L12 ordering and ?' precipitation in Al-Cu-Li.

Project description:The precipitation mechanism of the ?' (Al3Li) phase in Al-Li alloys has been controversially discussed in recent decades, specifically with respect to a conjectured congruent ordering process. However, kinetics in the Al-Li system does not allow to resolve the intermediate stages of precipitation and hence to experimentally clarify this issue. In this paper, we are revisiting the subject in ternary Al-Cu-Li alloys with pronouncedly slower kinetics, employing Transmission Electron Microscopy, High-Angle Annular Dark-Field Scanning Transmission Electron Microscopy, Differential Scanning Calorimetry and Atom Probe Tomography. The results show clear evidence for congruent ordering in a selected compositional range, revealing an already strongly L12 ordered microstructure after natural aging with a chemically homogeneous Li distribution and a decomposition of the alloy upon annealing at elevated temperatures. The presented study of the ?' precipitation evaluates the reaction pathway of this process and compares it to the predictions of the Bragg-Williams-Gorsky model with respect to decomposition and ordering in this alloy system.

| S-EPMC5468256 | biostudies-literature

Micromonospora endophytica (Xie et al. 2001) Li et al. 2019

Project description:Jishengella endophytica overview

| PRJNA489539 | ENA

Highly-Stable Li₄Ti₅O12 Anodes Obtained by Atomic-Layer-Deposited Al₂O₃.

Project description:LTO (Li₄Ti₅O12) has been highlighted as anode material for next-generation lithium ion secondary batteries due to advantages such as a high rate capability, excellent cyclic performance, and safety. However, the generation of gases from undesired reactions between the electrode surface and the electrolyte has restricted the application of LTO as a negative electrode in Li-ion batteries in electric vehicles (EVs) and energy storage systems (ESS). As the generation of gases from LTO tends to be accelerated at high temperatures (40⁻60 °C), the thermal stability of LTO should be maintained during battery discharge, especially in EVs. To overcome these technical limitations, a thin layer of Al₂O₃ (~2 nm thickness) was deposited on the LTO electrode surface by atomic layer deposition (ALD), and an electrochemical charge-discharge cycle test was performed at 60 °C. The capacity retention after 500 cycles clearly shows that Al₂O₃-coated LTO outperforms the uncoated one, with a discharge capacity retention of ~98%. TEM and XPS analyses indicate that the surface reactions of Al₂O₃-coated LTO are suppressed, while uncoated LTO undergoes the (111) to (222) phase transformation, as previously reported in the literature.

| S-EPMC5978180 | biostudies-literature

Optoelectronic synapses based on a triple cation perovskite and Al/MoO3 interface for neuromorphic information processing.

Project description:Optoelectronic synaptic transistors are attractive for applications in next-generation brain-like computation systems, especially for their visible-light operation and in-sensor computing capabilities. However, from a material perspective, it is difficult to build a device that meets expectations in terms of both its functions and power consumption, prompting the call for greater innovation in materials and device construction. In this study, we innovatively combined a novel perovskite carrier supply layer with an Al/MoO3 interface carrier regulatory layer to fabricate optoelectronic synaptic devices, namely Al/MoO3/CsFAMA/ITO transistors. The device could mimic a variety of biological synaptic functions and required ultralow-power consumption during operation with an ultrafast speed of >0.1 μs under an optical stimulus of about 3 fJ, which is equivalent to biological synapses. Moreover, Pavlovian conditioning and visual perception tasks could be implemented using the spike-number-dependent plasticity (SNDP) and spike-rate-dependent plasticity (SRDP). This study suggests that the proposed CsFAMA synapse with an Al/MoO3 interface has the potential for ultralow-power neuromorphic information processing.

| S-EPMC10790979 | biostudies-literature

Sensing of individual stalled 80S ribosomes by Fap1 for non-functional rRNA turnover. Li et al

Project description:Cells can respond to stalled ribosomes by sensing ribosome collisions and employing quality control pathways. How ribosome stalling is resolved without collisions, however, has remained elusive. Here, focusing on non-colliding stalling exhibited by decoding-defective ribosomes, we identified Fap1 as a stalling sensor triggering 18S non-functional rRNA decay via poly-ubiquitination of uS3. Ribosome profiling revealed an enrichment of Fap1 at the translation initiation site but also association with elongating individual ribosomes. Cryo-EM structures of Fap1-bound ribosomes elucidated Fap1 probing the mRNA simultaneously at both the entry and exit channels suggesting a mRNA stasis sensing activity, and Fap1 sterically hinders formation of canonical collided di-ribosomes. Our findings indicate that individual stalled ribosomes are the potential signal for ribosome dysfunction, leading to accelerated turnover of the ribosome itself.

2022-09-15 | GSE159329 | GEO

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