Analysis of charm meson semileptonic decays and charm baryon high mass states

1995 ◽  
Author(s):  
Luca Cinquini
1989 ◽  
Vol 578 (1 The Fourth Fa) ◽  
pp. 420-423
Author(s):  
R. PÉREZ-MARCIAL ◽  
R. HUERTA ◽  
A. GARCÍA ◽  
M. AVILA-AOKI

2006 ◽  
Vol 21 (27) ◽  
pp. 5482-5487
Author(s):  
James S. Russ

Heavy flavor baryons are attractive systems for testing effective theories for weak lifetime and decay systematics. Recently, new experimental results have mitigated one historic problem in the weak lifetime systematics and continued another. The charm baryon system continues to show new high mass, narrow states well isolated from one another. The spectroscopy of these states will challenge new advances in lattice gauge theoretic calculations of baryon structure. Double charm baryons still are seen only by SELEX, which showed a new [Formula: see text] candidate. High-sensitivity searches by BELLE and BaBar show only featureless background.


2015 ◽  
Vol 91 (9) ◽  
Author(s):  
Svjetlana Fajfer ◽  
Ivan Nišandžić ◽  
Urša Rojec

2009 ◽  
Vol 24 (supp01) ◽  
pp. 593-626 ◽  
Author(s):  
Hai-Yang Cheng

The following sections are included: Introduction Production of Charmed Baryons at BES-III Spectroscopy Strong Decays Lifetimes Hadronic Weak Decays Semileptonic Decays Electromagnetic and Weak Radiative Decays


2020 ◽  
Author(s):  
Urbi Pal ◽  
Fangfang Chen ◽  
Derick Gyabang ◽  
Thushan Pathirana ◽  
Binayak Roy ◽  
...  

We explore a novel ether aided superconcentrated ionic liquid electrolyte; a combination of ionic liquid, <i>N</i>-propyl-<i>N</i>-methylpyrrolidinium bis(fluorosulfonyl)imide (C<sub>3</sub>mpyrFSI) and ether solvent, <i>1,2</i> dimethoxy ethane (DME) with 3.2 mol/kg LiFSI salt, which offers an alternative ion-transport mechanism and improves the overall fluidity of the electrolyte. The molecular dynamics (MD) study reveals that the coordination environment of lithium in the ether aided ionic liquid system offers a coexistence of both the ether DME and FSI anion simultaneously and the absence of ‘free’, uncoordinated DME solvent. These structures lead to very fast kinetics and improved current density for lithium deposition-dissolution processes. Hence the electrolyte is used in a lithium metal battery against a high mass loading (~12 mg/cm<sup>2</sup>) LFP cathode which was cycled at a relatively high current rate of 1mA/cm<sup>2</sup> for 350 cycles without capacity fading and offered an overall coulombic efficiency of >99.8 %. Additionally, the rate performance demonstrated that this electrolyte is capable of passing current density as high as 7mA/cm<sup>2</sup> without any electrolytic decomposition and offers a superior capacity retention. We have also demonstrated an ‘anode free’ LFP-Cu cell which was cycled over 50 cycles and achieved an average coulombic efficiency of 98.74%. The coordination chemistry and (electro)chemical understanding as well as the excellent cycling stability collectively leads toward a breakthrough in realizing the practical applicability of this ether aided ionic liquid electrolytes in lithium metal battery applications, while delivering high energy density in a prototype cell.


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