Emilia Alwin
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Emilia Alwin has a total of 19 co-authors. Here are the top co-authors by number of shared publications:
- Mariusz Pietrowski
Faculty of Chemistry, Adam Mickiewicz University, Uniwersytetu Poznanskiego 8, 61-614 Poznan, Poland
9 shared publications - Michał Zieliński
Faculty of Chemistry, Adam Mickiewicz University, Uniwersytetu Poznanskiego 8, 61-614 Poznan, Poland
9 shared publications - Robert Wojcieszak
L2CM UMR 7053, Université de Lorraine, CNRS, Faculté des Sciences et Technologies, Vandœuvre-lès-Nancy, France
5 shared publications - Agata Suchora
Faculty of Chemistry, Adam Mickiewicz University, Poznań, Uniwersytetu Poznańskiego 8, 61-614 Poznań, Poland
3 shared publications - Kamila Kočí
Institute of Environmental Technology, Centre for Energy and Environmental Technologies, VSB - Technical University of Ostrava 2 , 17. listopadu 2172/15, 708 00 Ostrava-Poruba
2 shared publications - Miroslava Filip Edelmannova
Institute of Environmental Technology, Centre for Energy and Environmental Technologies, VSB - Technical University of Ostrava 2 , 17. listopadu 2172/15, 708 00 Ostrava-Poruba
2 shared publications
Latest Publications
- Open Access
- 5 December 2024
- Published by Royal Society of Chemistry (RSC) in Nanoscale Advances
- Vol. 7 (1) , 370
Expression of concern: In situ growth of N-doped carbon nanotubes from the products of graphitic carbon nitride etching by nickel nanoparticles
Expression of concern for ‘ In situ growth of N-doped carbon nanotubes from the products of graphitic carbon nitride etching by nickel nanoparticles’ by Mariusz Pietrowski et al. , Nanoscale Adv. , 2024, 6 , 1720–1726, https://doi.org/10.1039/D3NA00983A.
- 5 December 2024
- Published by Royal Society of Chemistry (RSC) in Nanoscale Advances
- Vol. 7 (1) , 370
Open AccessExpression of concern: In situ growth of N-doped carbon nanotubes from the products of graphitic carbon nitride etching by nickel nanoparticles
Expression of concern for ‘ In situ growth of N-doped carbon nanotubes from the products of graphitic carbon nitride etching by nickel nanoparticles’ by Mariusz Pietrowski et al. , Nanoscale Adv. , 2024, 6 , 1720–1726, https://doi.org/10.1039/D3NA00983A.
- Open Access
- 21 February 2024
- Published by Royal Society of Chemistry (RSC) in Nanoscale Advances
- Vol. 6 (6) , 1720-1726
In situ growth of N-doped carbon nanotubes from the products of graphitic carbon nitride etching by nickel nanoparticles
The products of g-C 3 N 4 etching are CH 4 , NH 3 , and HCN, which are used as building materials for N-doped carbon nanotubes without any external source of carbon or nitrogen.
- 21 February 2024
- Published by Royal Society of Chemistry (RSC) in Nanoscale Advances
- Vol. 6 (6) , 1720-1726
Open AccessIn situ growth of N-doped carbon nanotubes from the products of graphitic carbon nitride etching by nickel nanoparticles
The products of g-C 3 N 4 etching are CH 4 , NH 3 , and HCN, which are used as building materials for N-doped carbon nanotubes without any external source of carbon or nitrogen.
- Open Access
Reductive Modification of Carbon Nitride Structure by Metals—The Influence on Structure and Photocatalytic Hydrogen Evolution
Pt, Ru, and Ir were introduced onto the surface of graphitic carbon nitride (g-C3N4) using the wet impregnation method. A reduction of these photocatalysts with hydrogen causes several changes, such as a significant increase in the specific surface area, a C/N atomic ratio, a number of defects in the crystalline structure of g-C3N4, and the contribution of nitrogen bound to the amino and imino groups. According to the X-ray photoelectron spectroscopy results, a transition layer is formed at the g-C3N4/metal nanoparticle interphase, which contains metal at a positive degree of oxidation bonded to nitrogen. These structural changes significantly enhanced the photocatalytic activity in the production of hydrogen through the water-splitting reaction. The activity of the platinum photocatalyst was 24 times greater than that of pristine g-C3N4. Moreover, the enhanced activity was attributed to significantly better separation of photogenerated electron–hole pairs on metal nanoparticles and structural distortions of g-C3N4.
Open AccessReductive Modification of Carbon Nitride Structure by Metals—The Influence on Structure and Photocatalytic Hydrogen Evolution
Pt, Ru, and Ir were introduced onto the surface of graphitic carbon nitride (g-C3N4) using the wet impregnation method. A reduction of these photocatalysts with hydrogen causes several changes, such as a significant increase in the specific surface area, a C/N atomic ratio, a number of defects in the crystalline structure of g-C3N4, and the contribution of nitrogen bound to the amino and imino groups. According to the X-ray photoelectron spectroscopy results, a transition layer is formed at the g-C3N4/metal nanoparticle interphase, which contains metal at a positive degree of oxidation bonded to nitrogen. These structural changes significantly enhanced the photocatalytic activity in the production of hydrogen through the water-splitting reaction. The activity of the platinum photocatalyst was 24 times greater than that of pristine g-C3N4. Moreover, the enhanced activity was attributed to significantly better separation of photogenerated electron–hole pairs on metal nanoparticles and structural distortions of g-C3N4.
- 4 September 2020
- Published by Royal Society of Chemistry (RSC) in Dalton Transactions
- Vol. 49 (36) , 12805-12813
Elucidating the structure of the graphitic carbon nitride nanomaterials via X-ray photoelectron spectroscopy and X-ray powder diffraction techniques
Elucidating the layered structure of the g-C 3 N 4 nanomaterials using X-ray photoelectron spectroscopy and X-ray powder diffraction techniques is possible.
- 4 September 2020
- Published by Royal Society of Chemistry (RSC) in Dalton Transactions
- Vol. 49 (36) , 12805-12813
Elucidating the structure of the graphitic carbon nitride nanomaterials via X-ray photoelectron spectroscopy and X-ray powder diffraction techniques
Elucidating the layered structure of the g-C 3 N 4 nanomaterials using X-ray photoelectron spectroscopy and X-ray powder diffraction techniques is possible.
- Open Access
Influence of High Temperature Synthesis on the Structure of Graphitic Carbon Nitride and Its Hydrogen Generation Ability
Graphitic carbon nitride (g-C3N4) was obtained by thermal polymerization of dicyandiamide, thiourea or melamine at high temperatures (550 and 600 °C), using different heating rates (2 or 10 °C min−1) and synthesis times (0 or 4 h). The effects of the synthesis conditions and type of the precursor on the efficiency of g-C3N4 were studied. The most efficient was the synthesis from dicyandiamide, 53%, while the efficiency in the process of synthesis from melamine and thiourea were much smaller, 26% and 11%, respectively. On the basis of the results provided by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), infrared spectroscopy (FTIR), ultraviolet–visible spectroscopy (UV–vis), thermogravimetric analysis (TGA), elemental analysis (EA), the best precursor and the optimum conditions of synthesis of g-C3N4 were identified to get the product of the most stable structure, the highest degree of ordering and condensation of structure and finally the highest photocatalytic activity. It was found that as the proton concentration decreased and the degree of condensation increased, the hydrogen yields during the photocatalytic decomposition of water–methanol solution were significantly enhanced. The generation of hydrogen was 1200 µmol g−1 and the selectivity towards hydrogen of more than 98%.
Open AccessInfluence of High Temperature Synthesis on the Structure of Graphitic Carbon Nitride and Its Hydrogen Generation Ability
Graphitic carbon nitride (g-C3N4) was obtained by thermal polymerization of dicyandiamide, thiourea or melamine at high temperatures (550 and 600 °C), using different heating rates (2 or 10 °C min−1) and synthesis times (0 or 4 h). The effects of the synthesis conditions and type of the precursor on the efficiency of g-C3N4 were studied. The most efficient was the synthesis from dicyandiamide, 53%, while the efficiency in the process of synthesis from melamine and thiourea were much smaller, 26% and 11%, respectively. On the basis of the results provided by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), infrared spectroscopy (FTIR), ultraviolet–visible spectroscopy (UV–vis), thermogravimetric analysis (TGA), elemental analysis (EA), the best precursor and the optimum conditions of synthesis of g-C3N4 were identified to get the product of the most stable structure, the highest degree of ordering and condensation of structure and finally the highest photocatalytic activity. It was found that as the proton concentration decreased and the degree of condensation increased, the hydrogen yields during the photocatalytic decomposition of water–methanol solution were significantly enhanced. The generation of hydrogen was 1200 µmol g−1 and the selectivity towards hydrogen of more than 98%.
- 1 October 2019
- Published by Elsevier in Journal of Catalysis
- Vol. 378, 298-311
Cobalt-doped magnesium fluoride as a support for platinum catalysts: The correlation of surface acidity with hydrogenation activity
- 1 October 2019
- Published by Elsevier in Journal of Catalysis
- Vol. 378, 298-311
Cobalt-doped magnesium fluoride as a support for platinum catalysts: The correlation of surface acidity with hydrogenation activity
- Open Access
- 15 February 2019
- Published by Royal Society of Chemistry (RSC) in RSC Advances
- Vol. 9 (10) , 5711-5721
Synthesis and characterization of MgF2–CoF2 binary fluorides. Influence of the treatment atmosphere and temperature on the structure and surface properties
Results of the first research on structural and surface properties of binary fluorides MgF2–CoF2 are presented.
- 15 February 2019
- Published by Royal Society of Chemistry (RSC) in RSC Advances
- Vol. 9 (10) , 5711-5721
Open AccessSynthesis and characterization of MgF2–CoF2 binary fluorides. Influence of the treatment atmosphere and temperature on the structure and surface properties
Results of the first research on structural and surface properties of binary fluorides MgF2–CoF2 are presented.
- Open Access
- 22 August 2017
- Published by Springer Nature in Journal of Sol-Gel Science and Technology
- Vol. 84 (2) , 368-374
MgO-MgF2 system obtained by sol–gel method as an immobilizing agent of the electrolyte applied in the high temperature cells
- 22 August 2017
- Published by Springer Nature in Journal of Sol-Gel Science and Technology
- Vol. 84 (2) , 368-374
Open AccessMgO-MgF2 system obtained by sol–gel method as an immobilizing agent of the electrolyte applied in the high temperature cells
- 1 March 2017
- Published by Elsevier in Journal of Fluorine Chemistry
- Vol. 195, 18-25
A comparative study of the performance of Pt/MgF2, Ir/MgF2 and Ru/MgF2 catalysts in hydrogenation reactions
- 1 March 2017
- Published by Elsevier in Journal of Fluorine Chemistry
- Vol. 195, 18-25
A comparative study of the performance of Pt/MgF2, Ir/MgF2 and Ru/MgF2 catalysts in hydrogenation reactions