Browse
Submit Data
Databases
API
Help

Dataset Information

27 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Intramolecular water-splitting reaction in single collisions of water ions with surfaces.

ABSTRACT: We report the direct formation of H₂ and O pair ions through single collisions of water ions with metal surfaces at hyperthermal energies. This unusual intramolecular reaction proceeds also for heavy and semi-heavy water, producing molecular D₂ and HD ions. The selectivity of this water splitting channel is estimated at being between 9 and 13% versus complete dissociation. The collision kinematics support the hypothesis of a water molecule colliding with a single surface atom, thereby forming an excited precursor (Rydberg?) state, which dissociates subsequently to form the molecular hydrogen ion with high kinetic energy. Inelastic energy loss considerations yield an estimate for the energy of the excited precursor state of ?7 eV and ?11 eV at low and high incidence energies. These energies are close to the Ã state (¹B₁, 7.5 eV) and B state (¹A₁, 9.7 eV) of excited water (Rydberg states).

SUBMITTER: Yao Y

PROVIDER: S-EPMC5427682 | biostudies-literature | 2017 Apr

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Publications

Intramolecular water-splitting reaction in single collisions of water ions with surfaces.

Yao Yunxi Y Giapis Konstantinos P KP

Chemical science 20170118 4

We report the direct formation of H2 and O pair ions through single collisions of water ions with metal surfaces at hyperthermal energies. This unusual intramolecular reaction proceeds also for heavy and semi-heavy water, producing molecular D2 and HD ions. The selectivity of this water splitting channel is estimated at being between 9 and 13% versus complete dissociation. The collision kinematics support the hypothesis of a water molecule colliding with a single sur ...[more]

PMID: 28553523

Similar Datasets

Ribosome collisions trigger subunit splitting in E. coli

Project description:Although many clinically important antibiotics inhibit bacterial ribosomes, the mechanisms by which bacterial cells rescue ribosomes stalled by antibiotics remain poorly understood. Ribosome stalling leads to collisions that recruit ribosome quality control (RQC) factors that recycle the ribosome subunits and target nascent proteins for degradation. Surprisingly, loss of known RQC factors in E. coli does not lead to significant antibiotic sensitivity, even though antibiotics stall ribosomes and induce collisions, suggesting the existence of additional, uncharacterized RQC mechanisms. Here we report a novel mechanism for ribosome quality control (RQC) in bacteria in which the DExH-box ATPase HrpA splits stalled ribosomes into subunits. HrpA selectively acts on collided ribosomes and its activity is dependent on ATP hydrolysis. The cryo-EM structure of HrpA bound to collided ribosomes reveals insight into its selectivity and mechanism: the C-terminal domain of HrpA senses the collision and its helicase domain bind mRNA downstream of the ribosomes, where it likely exerts a pulling force that destabilizes the stalled ribosome. These studies highlight the importance of ribosome splitting as a highly conserved RQC mechanism across all three domains of life and identify an important pathway in proteobacteria that allows proteobacteria to tolerate ribosome-targeting antibiotics.

2024-10-10 | GSE270401 | GEO

Intramolecular Reaction of Transient Phosphenium and Arsenium Ions Giving Rise to Isolable 9-Phospha- and 9-Arsena-Fluorenium Ions.

Project description:Transient phosphenium and arsenium ions, generated by fluoride abstraction from bis(m-terphenyl)fluoropnictogens, underwent intramolecular electrophilic attack prior to methyl group migration and gave rise to isolable 9-phospha- and 9-arsena-fluorenium ions.

| S-EPMC7496934 | biostudies-literature

Water Splitting and Transport of Ions in Electromembrane System with Bilayer Ion-Exchange Membrane.

Project description:Bilayer ion-exchange membranes are mainly used for separating single and multiply charged ions. It is well known that in membranes in which the layers have different charges of the ionogenic groups of the matrix, the limiting current decreases, and the water splitting reaction accelerates in comparison with monolayer (isotropic) ion-exchange membranes. We study samples of bilayer ion-exchange membranes with very thin cation-exchange layers deposited on an anion-exchange membrane-substrate in this work. It was revealed that in bilayer membranes, the limiting current's value is determined by the properties of a thin surface film (modifying layer). A linear regularity of the dependence of the non-equilibrium effective rate constant of the water-splitting reaction on the resistance of the bipolar region, which is valid for both bilayer and bipolar membranes, has been revealed. It is shown that the introduction of the catalyst significantly reduces the water-splitting voltage, but reduces the selectivity of the membrane. It is possible to regulate the fluxes of salt ions and water splitting products (hydrogen and hydroxyl ions) by changing the current density. Such an ability makes it possible to conduct a controlled process of desalting electrolytes with simultaneous pH adjustment.

| S-EPMC7697576 | biostudies-literature

Photocorrosion of ZnO Single Crystals during Electrochemical Water Splitting.

Project description:Degradation and dissolution of transparent semiconducting oxides is central to various areas, including design of catalysts and catalysis conditions, as well as passivation of metal surfaces. In particular, photocorrosion can be significant and plays a central role during photoelectrochemical activity of transparent semiconducting oxides. Here, we utilize an electrochemical flow cell combined with an inductively coupled plasma mass spectrometer (ICP-MS) to enable the in situ study of the time-resolved release of zinc into solution under simultaneous radiation of UV-light. With this system we study the dissolution of zinc oxide single crystals with (0001) and (101̅0) orientations. At acidic and alkaline pH, we characterized potential dependent dissolution rates into both the oxygen and the hydrogen evolving conditions. A significant influence of the UV radiation and the pH of the electrolyte was observed. The observed dissolution behavior agrees well with the surface chemistry and stabilization mechanism of ZnO surfaces. In particular, polar ZnO(0001) shows ideal stability at low potentials and under hydrogen evolution conditions. Whereas ZnO(101̅0) sustains higher dissolution rates, while it is inactive for water splitting. Our data demonstrates that surface design and fundamental understanding of surface chemistry provides an effective path to rendering electroactive surfaces stable under operating conditions.

| S-EPMC7688208 | biostudies-literature

Specific ions modulate diffusion dynamics of hydration water on lipid membrane surfaces.

Project description:Effects of specific ions on the local translational diffusion of water near large hydrophilic lipid vesicle surfaces were measured by Overhauser dynamic nuclear polarization (ODNP). ODNP relies on an unpaired electron spin-containing probe located at molecular or surface sites to report on the dynamics of water protons within ~10 Å from the spin probe, which give rise to spectral densities for electron-proton cross-relaxation processes in the 10 GHz regime. This pushes nuclear magnetic resonance relaxometry to more than an order of magnitude higher frequencies than conventionally feasible, permitting the measurement of water moving with picosecond to subnanosecond correlation times. Diffusion of water within ~10 Å of, i.e., up to ~3 water layers around the spin probes located on hydrophilic lipid vesicle surfaces is ~5 times retarded compared to the bulk water translational diffusion. This directly reflects on the activation barrier for surface water diffusion, i.e., how tightly water is bound to the hydrophilic surface and surrounding waters. We find this value to be modulated by the presence of specific ions in solution, with its order following the known Hofmeister series. While a molecular description of how ions affect the hydration structure at the hydrophilic surface remains to be answered, the finding that Hofmeister ions directly modulate the surface water diffusivity implies that the strength of the hydrogen bond network of surface hydration water is directly modulated on hydrophilic surfaces.

| S-EPMC3985948 | biostudies-literature

Single-crystalline, wormlike hematite photoanodes for efficient solar water splitting.

Project description:A hematite photoanode showing a stable, record-breaking performance of 4.32?mA/cm² photoelectrochemical water oxidation current at 1.23?V vs. RHE under simulated 1-sun (100?mW/cm²) irradiation is reported. This photocurrent corresponds to ca. 34% of the maximum theoretical limit expected for hematite with a band gap of 2.1?V. The photoanode produced stoichiometric hydrogen and oxygen gases in amounts close to the expected values from the photocurrent. The hematitle has a unique single-crystalline "wormlike" morphology produced by in-situ two-step annealing at 550°C and 800°C of ?-FeOOH nanorods grown directly on a transparent conducting oxide glass via an all-solution method. In addition, it is modified by platinum doping to improve the charge transfer characteristics of hematite and an oxygen-evolving co-catalyst on the surface.

| S-EPMC3775410 | biostudies-literature

Stereoselective and regioselective intramolecular Friedel-Crafts reaction of aziridinium ions for synthesis of 4-substituted tetrahydroisoquinolines.

Project description:Optically active 4-substituted tetrahydroisoquinolines were synthesized via intramolecular Friedel-Crafts (FC) reactions of aziridinium ions in a highly regio- and stereoselective manner. Control experiments suggest the formation and ring-opening of aziridinium ions as the key intermediates in the Lewis acid catalyzed FC reactions.

| S-EPMC6423956 | biostudies-literature

Ribosome collisions trigger subunit splitting in E. coli

Project description:Ribosome collisions trigger subunit splitting in E. coli

| PRJNA1126309 | ENA

Plasmon-Induced Water Splitting on Ag-Alloyed Pt Single-Atom Catalysts.

Project description:A promising route to realize solar-to-chemical energy conversion resorts to water splitting using plasmon photocatalysis. However, the ultrafast carrier dynamics and underlying mechanism in such processes has seldom been investigated, especially when the single-atom catalyst is introduced. Here, from the perspective of quantum dynamics at the atomic length scale and femtosecond time scale, we probe the carrier and structural dynamics of plasmon-assisted water splitting on an Ag-alloyed Pt single-atom catalyst, represented by the Ag19Pt nanocluster. The substitution of an Ag atom by the Pt atom at the tip of the tetrahedron Ag20 enhances the interaction between water and the nanoparticle. The excitation of localized surface plasmons in the Ag19Pt cluster strengthens the charge separation and electron transfer upon illumination. These facts cooperatively turn on more than one charge transfer channels and give rise to enhanced charge transfer from the metal nanoparticle to the water molecule, resulting in rapid plasmon-induced water splitting. These results provide atomistic insights and guidelines for the design of efficient single-atom photocatalysts for plasmon-assisted water splitting.

| S-EPMC8573343 | biostudies-literature

Reaction kinetics of ultracold molecule-molecule collisions.

Project description:Studying chemical reactions on a state-to-state level tests and improves our fundamental understanding of chemical processes. For such investigations it is convenient to make use of ultracold atomic and molecular reactants as they can be prepared in well defined internal and external quantum states. Here, we investigate a single-channel reaction of two Li2-Feshbach molecules where one of the molecules dissociates into two atoms 2AB???AB?+?A?+?B. The process is a prototype for a class of four-body collisions where two reactants produce three product particles. We measure the collisional dissociation rate constant of this process as a function of collision energy/temperature and scattering length. We confirm an Arrhenius-law dependence on the collision energy, an a4 power-law dependence on the scattering length a and determine a universal four body reaction constant.

| S-EPMC6286306 | 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