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Featured researches published by Andrzej Kulka.


Materials | 2013

Structural, Transport and Electrochemical Properties of LiFePO4 Substituted in Lithium and Iron Sublattices (Al, Zr, W, Mn, Co and Ni)

Janina Molenda; Andrzej Kulka; Anna Milewska; Wojciech Zając; Konrad Świerczek

LiFePO4 is considered to be one of the most promising cathode materials for lithium ion batteries for electric vehicle (EV) application. However, there are still a number of unsolved issues regarding the influence of Li and Fe-site substitution on the physicochemical properties of LiFePO4. This is a review-type article, presenting results of our group, related to the possibility of the chemical modification of phosphoolivine by introduction of cation dopants in Li and Fe sublattices. Along with a synthetic review of previous papers, a large number of new results are included. The possibility of substitution of Li+ by Al3+, Zr4+, W6+ and its influence on the physicochemical properties of LiFePO4 was investigated by means of XRD, SEM/EDS, electrical conductivity and Seebeck coefficient measurements. The range of solid solution formation in Li1−3xAlxFePO4, Li1−4xZrxFePO4 and Li1−6xWxFePO4 materials was found to be very narrow. Transport properties of the synthesized materials were found to be rather weakly dependent on the chemical composition. The battery performance of selected olivines was tested by cyclic voltammetry (CV). In the case of LiFe1−yMyPO4 (M = Mn, Co and Ni), solid solution formation was observed over a large range of y (0 < y ≤ 1). An increase of electrical conductivity for the substitution level y = 0.25 was observed. Electrons of 3d metals other than iron do not contribute to the electrical properties of LiFe1−yMyPO4, and substitution level y > 0.25 leads to considerably lower values of σ. The activated character of electrical conductivity with a rather weak temperature dependence of the Seebeck coefficient suggests a small polaron-type conduction mechanism. The electrochemical properties of LiFe1−yMyPO4 strongly depend on the Fe substitution level.


Functional Materials Letters | 2011

INVESTIGATION OF GdBaCo2-xFexO5.5-δ AS A CATHODE MATERIAL FOR INTERMEDIATE TEMPERATURE SOLID OXIDE FUEL CELLS

Andrzej Kulka; Yang Hu; Guilhem Dezanneau; Janina Molenda

In this work, we present an evaluation of the layered perovskite materials with chemical composition GdBaCo2-xFexO5.5-δ (x = 0.0, 0.3, 0.6) as a cathode materials for intermediate temperature solid oxide fuel cell (IT-SOFC). We first present results concerning their crystal structure and oxygen nonstoichiometry, and then give results concerning their electrical conductivity and performance in button-type SOFCs.


Functional Materials Letters | 2016

Enhancement of electrochemical performance of LiFePO4 nanoparticles by direct nanocoating with conductive carbon layers

Joanna Świder; Marcin Molenda; Andrzej Kulka; Janina Molenda

The results of simple and environmental-friendly method of the carbon nanocoatings on low-conductive cathode material have been shown in this work. The carbon nanocoatings were prepared during wet impregnation process of precursor derived from hydrophilic polymer based on poly(N-vinylformamide) modified by pyromellitic acid. The crystal structures and morphology of all composites were characterized by X-ray powder diffraction (XRD), low temperature nitrogen adsorption/desorption measurements (N2-BET) and transmission electronic microscopy (TEM). The electrical properties of the obtained composites were examined by EC studies. The electrochemical performance was carried out in galvanostatic mode with stable charge–discharge current and performed in Li/Li+/(CCL/LiFePO4) type cells. The process of formation CCL/LiFePO4 nanocomposite significantly enhances the electrical conductivity of the material and improves its capacity retention and electrochemical performance.


Electrochimica Acta | 2015

Facile synthesis of MoO3/carbon nanobelts as high-performance anode material for lithium ion batteries

Qing Xia; Hailei Zhao; Zhihong Du; Zhipeng Zeng; Chunhui Gao; Zijia Zhang; Xuefei Du; Andrzej Kulka; Konrad Świerczek


Electrochimica Acta | 2017

Synthesis of core-shell-like ZnS/C nanocomposite as improved anode material for lithium ion batteries

Xuefei Du; Hailei Zhao; Yao Lu; Zijia Zhang; Andrzej Kulka; Konrad Świerczek


Solid State Ionics | 2015

Evidence for Al doping in lithium sublattice of LiFePO4

Andrzej Kulka; Artur Braun; Tzu-Wen Huang; A. Wolska; Marcin T. Klepka; A. Szewczyk; Dominika Baster; Wojciech Zając; Konrad Świerczek; Janina Molenda


Solid State Ionics | 2012

Possibility of modification of phosphoolivine by substitution in Li sublattice

Andrzej Kulka; Anna Milewska; Wojciech Zając; Konrad Świerczek; Emil Hanc; Janina Molenda


Acta Materialia | 2015

Characterization of the physicochemical properties of novel SnS2 with cubic structure and diamond-like Sn sublattice

Xin Liu; Hailei Zhao; Andrzej Kulka; Anita Trenczek-Zając; Jingying Xie; Ning Chen; Konrad Świerczek


Journal of Power Sources | 2013

Electrochemical properties of chemically modified phosphoolivines as cathode materials for Li-ion batteries

Andrzej Kulka; Dominika Baster; Michał Dudek; Michał Kiełbasa; Anna Milewska; Wojciech Zając; Konrad Świerczek; Janina Molenda


Solid State Ionics | 2016

Correlation between transport properties and lithium extraction/insertion mechanism in Fe-site substituted phosphoolivine

Andrzej Kulka; Konrad Świerczek; Katarzyna Walczak; Artur Braun; Janina Molenda

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Janina Molenda

AGH University of Science and Technology

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Konrad Świerczek

AGH University of Science and Technology

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Wojciech Zając

AGH University of Science and Technology

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Anna Milewska

AGH University of Science and Technology

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Katarzyna Walczak

AGH University of Science and Technology

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Hailei Zhao

University of Science and Technology Beijing

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Dominika Baster

AGH University of Science and Technology

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Łukasz Kondracki

AGH University of Science and Technology

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Artur Braun

Swiss Federal Laboratories for Materials Science and Technology

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Xuefei Du

University of Science and Technology Beijing

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