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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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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University of Exeter

in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (8/8 displayed)

  • 2024Investigation of the Dynamic Behaviour of H 2 and D 2 in a Kinetic Quantum Sieving System2citations
  • 2024Investigation of the Dynamic Behaviour of H 2 and D 2 in a Kinetic Quantum Sieving System2citations
  • 2022Manipulation of the crystalline phase diagram of hydrogen through nanoscale confinement effects in porous carbons12citations
  • 2022Manipulation of the crystalline phase diagram of hydrogen through nanoscale confinement effects in porous carbons12citations
  • 2021Solvent sorption-induced actuation of composites based on a polymer of intrinsic microporosity11citations
  • 2021Solvent Sorption-Induced Actuation of Composites Based on a Polymer of Intrinsic Microporosity11citations
  • 2018Enhanced adsorption of cationic and anionic dyes from aqueous solutions by polyacid doped polyaniline77citations
  • 2018Enhanced adsorption of cationic and anionic dyes from aqueous solutions by polyacid doped polyaniline77citations

Places of action

Chart of shared publication
Ting, V. P.
2 / 9 shared
Rochat, Sebastien
4 / 10 shared
Olivier, Jacques
2 / 2 shared
Kulak, Alexander
2 / 5 shared
Doan, Huan V.
1 / 6 shared
Yang, Anna
2 / 2 shared
Krzystyniak, Matthew
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Bending, Simon J.
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Terry, Lui
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Silva, Ivan Da
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Rols, Stephane
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Da Silva, Ivan
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Terry, Lui R.
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Gathercole, Nicholas
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Bowen, Cr
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Polak-Kraśna, Katarzyna
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Burrows, Andrew
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Yuan, Chenggang
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Mays, Tj
1 / 1 shared
Hao, Zhe
2 / 2 shared
Pan, Min
2 / 4 shared
Bowen, Christopher R.
1 / 96 shared
Burrows, Andrew D.
1 / 17 shared
Mays, Timothy J.
1 / 17 shared
Amura, Ida
2 / 2 shared
Sarihan, Adem
2 / 2 shared
Emanuelsson, Emma
1 / 2 shared
Shen, Junjie
2 / 3 shared
Emanuelsson, Emma A. C.
1 / 1 shared
Shahid, Salman
1 / 7 shared
Chart of publication period
2024
2022
2021
2018

Co-Authors (by relevance)

  • Ting, V. P.
  • Rochat, Sebastien
  • Olivier, Jacques
  • Kulak, Alexander
  • Doan, Huan V.
  • Yang, Anna
  • Krzystyniak, Matthew
  • Bending, Simon J.
  • Terry, Lui
  • Silva, Ivan Da
  • Rols, Stephane
  • Da Silva, Ivan
  • Terry, Lui R.
  • Gathercole, Nicholas
  • Bowen, Cr
  • Polak-Kraśna, Katarzyna
  • Burrows, Andrew
  • Yuan, Chenggang
  • Mays, Tj
  • Hao, Zhe
  • Pan, Min
  • Bowen, Christopher R.
  • Burrows, Andrew D.
  • Mays, Timothy J.
  • Amura, Ida
  • Sarihan, Adem
  • Emanuelsson, Emma
  • Shen, Junjie
  • Emanuelsson, Emma A. C.
  • Shahid, Salman
OrganizationsLocationPeople

article

Investigation of the Dynamic Behaviour of H 2 and D 2 in a Kinetic Quantum Sieving System

  • Rochat, Sebastien
  • Olivier, Jacques
  • Kulak, Alexander
  • Yang, Anna
  • Tian, Mi
  • Krzystyniak, Matthew
Abstract

Porous organic cages (POCs) are nanoporous materials composed of discrete molecular units that have uniformly distributed functional pores. The intrinsic porosity of these structures can be tuned accurately at the nanoscale by altering the size of the porous molecules, particularly to an optimal size of 3.6 Å, to harness the kinetic quantum sieving effect. Previous research on POCs for isotope separation has predominantly centered on differences in the quantities of adsorbed isotopes. However, nuclear quantum effects also contribute significantly to the dynamics of the sorption process, offering additional opportunities for separating H2 and D2 at practical operational temperatures. In this study, our investigations into H2 and D2 sorption on POC samples revealed a higher uptake of D2 compared to that of H2 under identical conditions. We employed quasi-elastic neutron scattering to study the diffusion processes of D2 and H2 in the POCs across various temperature and pressure ranges. Additionally, neutron Compton scattering was utilized to measure the values of the nuclear zero-point energy of individual isotopic species in D2 and H2. The results indicate that the diffusion coefficient of D2 is approximately one-sixth that of H2 in the POC due to the nuclear quantum effect. Furthermore, the results reveal that at 77 K, D2 has longer residence times compared to H2 when moving from pore to pore. Consequently, using the kinetic difference of H2 and D2 in a porous POC system enables hydrogen isotope separation using a temperature or pressure swing system at around liquid nitrogen temperatures.

Topics
  • porous
  • impedance spectroscopy
  • pore
  • Nitrogen
  • Hydrogen
  • porosity
  • Elastic neutron scattering