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Jin-Ho Kim

Publications and source records attributed to Jin-Ho Kim.

2 recordsLinked to original sources

Quasiparticle Screening near a Bosonic Superconductor-Insulator Transition Revealed by Magnetic Impurity Doping

Experiments show that the Cooper pair transport in the insulator phase that forms at thin film superconductor to insulator transitions (SIT) is simply activated. This activated behavior depends on the microscopic factors that drive the localization of the Cooper pairs. To test proposed models, we investigated how a perturbation that weakens Cooper pair binding, magnetic impurity doping, affects the characteristic activation energy, $T_0$. The data show that $T_0$ decreases monotonically with doping in films tuned farther from the SIT and increases and peaks in films that are closer to the SIT critical point. These observations provide strong evidence that the bosonic SIT in thin films is a Mott transition driven by Coulomb interactions that are screened by virtual quasi-particle excitations. This dependence on underlying fermionic degrees of freedom distinguishes these SITs from those in micro-fabricated Josephson Junction Arrays, cold atom systems, and likely in high temperature superconductors with nodes in their quasiparticle density of states.

cond-mat.supr-con

Identifiability and parameter estimation of the single particle lithium-ion battery model

This paper investigates the identifiability and estimation of the parameters of the single particle model (SPM) for lithium-ion battery simulation. Identifiability is addressed both in principle and in practice. The approach begins by grouping parameters and partially non-dimensionalising the SPM to determine the maximum expected degrees of freedom in the problem. We discover that, excluding open circuit voltage, there are only six independent parameters. We then examine the structural identifiability by considering whether the transfer function of the linearised SPM is unique. It is found that the model is unique provided that the electrode open circuit voltage functions have a known non-zero gradient, the parameters are ordered, and the electrode kinetics are lumped into a single charge transfer resistance parameter. We then demonstrate the practical estimation of model parameters from measured frequency-domain experimental electrochemical impedance spectroscopy (EIS) data, and show additionally that the parametrised model provides good predictive capabilities in the time domain, exhibiting a maximum voltage error of 20 mV between model and experiment over a 10 minute dynamic discharge.

eess.SY