Katarzyna Lota

Dr. Katarzyna Lota

orcid

Research Focus & Metrics

Academic Career Length

23Years (2004-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 February 2006 in Journal of Power Sources
Verified
Journal Article
Closed access
EFE. Frackowiak
E. Frackowiak
VKVolodymyr Khomenko
Volodymyr Khomenko
KJK. Jurewicz
K. Jurewicz
KLKatarzyna Lota
Katarzyna Lota
FBF. Béguin
F. Béguin

1 March 2004 in Journal of Physics and Chemistry of Solids
Verified
Journal Article
Closed access
KLKatarzyna Lota
Katarzyna Lota
VKVolodymyr Khomenko
Volodymyr Khomenko
EFE. Frackowiak
E. Frackowiak

1 July 2007 in Electrochemistry Communications
Verified
Journal Article
Closed access
GLGrzegorz Lota
Grzegorz Lota
KLKatarzyna Lota
Katarzyna Lota
EFElzbieta Frackowiak
Elzbieta Frackowiak

2 June 2020 in Advanced Energy Materials
Verified
Journal Article
Open access
PDF file
RARachid Amine
Rachid Amine
JLJianzhao Liu
Jianzhao Liu
IAIlona Acznik
Ilona Acznik
TSTian Sheng
Tian Sheng
KLKatarzyna Lota
Katarzyna Lota
GXGui‐Liang Xu
Gui‐Liang Xu
Lithium–sulfur batteries are attractive for automobile and grid applications due to their high theoretical energy density and the abundance of sulfur. Despite the significant progress in cathode development, lithium metal degradation and the polysulfide shuttle remain two critical challenges in the practical application of Li–S batteries. Development of advanced electrolytes has become a promising strategy to simultaneously suppress lithium dendrite formation and prevent polysulfide dissolution. Here, a new class of concentrated siloxane‐based electrolytes, demonstrating significantly improved performance over the widely investigated ether‐based electrolytes are reported in terms of stabilizing the sulfur cathode and Li metal anode as well as minimizing flammability. Through a combination of experimental and computational investigation, it is found that siloxane solvents can effectively regulate a hidden solvation‐ion‐exchange process in the concentrated electrolytes that results from the interactions between cations/anions (e.g., Li+, TFSI−, and S2−) and solvents. As a result, it could invoke a quasi‐solid‐solid lithiation and enable reversible Li plating/stripping and robust solid‐electrolyte interphase chemistries. The solvation‐ion‐exchange process in the concentrated electrolytes is a key factor in understanding and designing electrolytes for other high‐energy lithium metal batteries.

15 November 2010 in Journal of Power Sources
Verified
Journal Article
Closed access
GLGrzegorz Lota
Grzegorz Lota
Jacek TyczkowskiJacek Tyczkowski
Jacek Tyczkowski
RKRyszard Kapica
Ryszard Kapica
KLKatarzyna Lota
Katarzyna Lota
EFElzbieta Frackowiak
Elzbieta Frackowiak

22 June 2016 in Journal of Solid State Electrochemistry
Verified
Journal Article
Open access
PDF file
GLGrzegorz Lota
Grzegorz Lota
Piotr KrawczykPiotr Krawczyk
Piotr Krawczyk
KLKatarzyna Lota
Katarzyna Lota
ASAgnieszka Sierczyńska
Agnieszka Sierczyńska
ŁKŁukasz Kolanowski
Łukasz Kolanowski
Tomasz BuchwaldTomasz Buchwald
Tomasz Buchwald

Abstract

Activated carbon modified by ozone treatment was examined. The process was carried out in a glass reactor under a continuous flow of ozone through a bed of activated carbon for 15, 30, 60, 120, and 240 min. The modified and unmodified carbon materials were characterized by Raman spectroscopy and observed by scanning electron microscopy (SEM). Thermogravimetric analysis was used to estimate the presence of oxygen groups in the carbon structure. The surface area and pore size distribution were examined by nitrogen adsorption method at 77 K. Moreover, Fourier transform infrared (FTIR) spectroscopy was used to estimate the functional groups of modified activated carbon. The carbon content was estimated using the elemental analysis. The process of ozonation increases oxygen functionalities, thus the activated carbon was tested as electrodes for an electrochemical capacitor. The performance of an electrochemical capacitor was estimated by selected alternating (AC) and direct current (DC) methods in 1 M H2SO4, 1 M Na2SO4, and 6 M KOH electrolytes.

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