Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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Materials Map under construction

The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (3/3 displayed)

  • 2023Mono-, bi- and tri-metallic platinum group metal-free electrocatalysts for hydrogen evolution reaction following a facile synthetic route15citations
  • 2023Defect Engineering of Ta3N5 Photoanodes: Enhancing Charge Transport and Photoconversion Efficiencies via Ti Doping13citations
  • 2023Use of copper carbonate as corrosion inhibitor for carbon steel in post combustion carbon capture3citations

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Chart of shared publication
Santamaria, Monica
1 / 50 shared
Santoro, Carlo
1 / 6 shared
Lavacchi, Alessandro
1 / 11 shared
Galli, Anna
1 / 4 shared
Capozzoli, Laura
1 / 1 shared
Muhyuddin, Mohsin
1 / 3 shared
Berretti, Enrico
1 / 7 shared
Vecchio, Carmelo Lo
1 / 1 shared
Mirshokraee, Seyed Ariana
1 / 2 shared
Zaffora, Andrea
1 / 15 shared
Orsilli, Jacopo
1 / 1 shared
Franco, Francesco Di
1 / 2 shared
Baglio, Vincenzo
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Olivi, Luca
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Grötzner, Gabriel
1 / 1 shared
Brune, Oliver
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Munnik, Frans
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Wagner, Laura I.
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Sharp, Ian
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Eichhorn, Johanna
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Sirotti, Elise Ida
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Streibel, Verena
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Santra, Saswati
1 / 2 shared
Alsalem, Mustafa M.
1 / 1 shared
Booth, Samuel G.
1 / 1 shared
Skountzos, Epameinondas
1 / 1 shared
Parlett, Christopher M. A.
1 / 9 shared
Price, Cameron A.
1 / 1 shared
Cussen, Serena A.
1 / 2 shared
Sedransk Campbell, Kyra L.
1 / 2 shared
Chart of publication period
2023

Co-Authors (by relevance)

  • Santamaria, Monica
  • Santoro, Carlo
  • Lavacchi, Alessandro
  • Galli, Anna
  • Capozzoli, Laura
  • Muhyuddin, Mohsin
  • Berretti, Enrico
  • Vecchio, Carmelo Lo
  • Mirshokraee, Seyed Ariana
  • Zaffora, Andrea
  • Orsilli, Jacopo
  • Franco, Francesco Di
  • Baglio, Vincenzo
  • Olivi, Luca
  • Grötzner, Gabriel
  • Brune, Oliver
  • Munnik, Frans
  • Wagner, Laura I.
  • Sharp, Ian
  • Eichhorn, Johanna
  • Sirotti, Elise Ida
  • Streibel, Verena
  • Santra, Saswati
  • Alsalem, Mustafa M.
  • Booth, Samuel G.
  • Skountzos, Epameinondas
  • Parlett, Christopher M. A.
  • Price, Cameron A.
  • Cussen, Serena A.
  • Sedransk Campbell, Kyra L.
OrganizationsLocationPeople

article

Defect Engineering of Ta3N5 Photoanodes: Enhancing Charge Transport and Photoconversion Efficiencies via Ti Doping

  • Grötzner, Gabriel
  • Brune, Oliver
  • Pollastri, Simone
  • Munnik, Frans
  • Wagner, Laura I.
  • Sharp, Ian
  • Eichhorn, Johanna
  • Sirotti, Elise Ida
  • Streibel, Verena
  • Olivi, Luca
  • Santra, Saswati
Abstract

<jats:title>Abstract</jats:title><jats:p>While Ta<jats:sub>3</jats:sub>N<jats:sub>5</jats:sub> shows excellent potential as a semiconductor photoanode for solar water splitting, its performance is hindered by poor charge carrier transport and trapping due to native defects that introduce electronic states deep within its bandgap. Here, it is demonstrated that controlled Ti doping of Ta<jats:sub>3</jats:sub>N<jats:sub>5</jats:sub> can dramatically reduce the concentration of deep‐level defects and enhance its photoelectrochemical performance, yielding a sevenfold increase in photocurrent density and a 300 mV cathodic shift in photocurrent onset potential compared to undoped material. Comprehensive characterization reveals that Ti<jats:sup>4+</jats:sup> ions substitute Ta<jats:sup>5+</jats:sup> lattice sites, thereby introducing compensating acceptor states, reducing the concentrations of deleterious nitrogen vacancies and reducing Ta<jats:sup>3+</jats:sup> states, and thereby suppressing trapping and recombination. Owing to the similar ionic radii of Ti<jats:sup>4+</jats:sup> and Ta<jats:sup>5+</jats:sup>, substitutional doping does not introduce lattice strain or significantly affect the underlying electronic structure of the host semiconductor. Furthermore, Ti can be incorporated without increasing the oxygen donor content, thereby enabling the electrical conductivity to be tuned by over seven orders of magnitude. Thus, Ti doping of Ta<jats:sub>3</jats:sub>N<jats:sub>5</jats:sub> provides a powerful basis for precisely engineering its optoelectronic characteristics and to substantially improve its functional characteristics as an advanced photoelectrode for solar fuels applications.</jats:p>

Topics
  • density
  • impedance spectroscopy
  • Oxygen
  • semiconductor
  • Nitrogen
  • defect
  • electrical conductivity