We show that strong molecular rotation drastically modifies the autodetachment of C_{2}^{-} ions in the lowest quartet electronic state a^{4}Σ_{u}^{+}. In the strong-rotation regime, levels of this state only decay by a process termed "rotationally assisted" autodetachment, whose theoretical description is worked out based on the nonlocal resonance model. For autodetachment linked with the exchange of six rotational quanta, the results reproduce a prominent, hitherto unexplained electron emission signal with a mean decay time near 3 ms, observed on stored C_{2}^{-} ions from a hot ion source.

Download full-text PDF

Source
http://dx.doi.org/10.1103/PhysRevLett.133.183001DOI Listing

Publication Analysis

Top Keywords

c_{2}^{-} ions
8
autodetachment
4
autodetachment diatomic
4
diatomic carbon
4
carbon anions
4
anions long-lived
4
long-lived high-rotation
4
high-rotation quartet
4
quartet states
4
states strong
4

Similar Publications

2D materials feature large specific surface areas and abundant active sites, showing great potential in energy storage and conversion. However, the dense, stacked structure severely restricts its practical application. Inspired by the structure of bamboo in nature, hollow interior and porous exterior wall, hollow MXene aerogel fiber (HA-TiCT fiber) is proposed.

View Article and Find Full Text PDF

Additives-Modified Electrodeposition for Synthesis of Hydrophobic Cu/CuO with Ag Single Atoms to Drive CO Electroreduction.

Adv Mater

January 2025

State Key Laboratory of Petroleum Molecular & Process Engineering, Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering, East China Normal University, Shanghai, 200062, China.

Copper-based electrocatalysts are recognized as crucial catalysts for CO electroreduction into multi-carbon products. However, achieving copper-based electrocatalysts with adjustable valences via one-step facile synthesis remains a challenge. In this study, Cu/CuO heterostructure is constructed by adjusting the anion species of the Cu ions-containing electrolyte during electrodeposition synthesis.

View Article and Find Full Text PDF

Hydraulic structures are frequently subjected to soft-water or acidic environments, necessitating serious consideration of the long-term effects of calcium leaching on the durability of concrete structures. Three types of common Portland cement (ordinary Portland cement, moderate-heat cement, and low-heat cement) paste samples widely applied to hydraulic concrete were immersed in a 6 mol/L NHCl solution to simulate accelerated calcium leaching behavior. The mass loss, porosity, leaching depth, compressive strength, and Ca/Si ratio of the three types of pastes were measured at different immersion stages (0, 14, 28, 56, 91, 140, and 180 days).

View Article and Find Full Text PDF

In the binuclear title complex, [La(CHO)(CHN)(HO)](NO)·0.5HO, the two lanthanum ions are nine coordinate in a distorted trigonal-prismatic geometry. Each La ion is bonded to three N atoms of the Schiff base, 1-(pyridin-2-yl)-2-(pyridin-2-yl-methyl-ene)hydrazine and is coordinated by one acetate group, which acts in -bidentate mode and two acetate groups that act in -mode between the two La ions.

View Article and Find Full Text PDF
Article Synopsis
  • The study uses molecular dynamics simulations to analyze how different termination functional groups on TiCT MXene membranes affect the behavior of nearby water molecules and foulants.
  • Results indicate that a denser water layer forms near hydroxyl (OH) terminated membranes compared to fluorine (F) or oxygen (O) terminations, influencing the binding of alginate monomers.
  • Steered molecular dynamics simulations reveal that M alginate monomers bind more strongly to O terminated surfaces, while binding is weak near OH terminations due to hydration water, with calcium ions enhancing fouling via contact and solvent-shared ionic pairs.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!