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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Lancaster University

in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (7/7 displayed)

  • 2022Efficient solid-state photoswitching of methoxyazobenzene in a metal–organic framework for thermal energy storage18citations
  • 2022A structural investigation of organic battery anode materials by NMR crystallography7citations
  • 2021Solid-state nuclear magnetic resonance study of polymorphism in tris(8-hydroxyquinolinate)aluminium2citations
  • 2021Effect of Transition Metal Substitution on the Flexibility and Thermal Properties of MOF-Based Solid-Solid Phase Change Materials10citations
  • 2020Long-Term Solar Energy Storage under Ambient Conditions in a MOF-Based Solid–Solid Phase-Change Material44citations
  • 2016Towards Robust Electroactive Biomaterialscitations
  • 2014Arylspiroborates derived from 4-tert-Butylcatechol and 3,5-Di-tertbutylcatechol and their antimicrobial activities8citations

Places of action

Chart of shared publication
Griffiths, Kieran
4 / 5 shared
Griffin, John
2 / 4 shared
Desai, Aamod V.
1 / 1 shared
Seymour, Valerie Ruth
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Griffin, John M.
1 / 7 shared
Morris, Russell E.
1 / 30 shared
Whewell, Tommy
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Armstrong, A. Robert
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Griffin, J. M.
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Cervini, L.
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Shah, Sayed
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Robinson, Bj
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Firlak, Melike
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Geier, Michael J.
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Westcott, Stephen A.
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Lee, Graham M.
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Decken, Andreas
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Oneill, Taryn
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Webb, Michael I.
1 / 1 shared
Vogels, Christopher M.
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Bowes, Eric G.
1 / 1 shared
Flewelling, Andrew
1 / 1 shared
Gray, Christopher A.
1 / 1 shared
Li, Haoxin
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2021
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Co-Authors (by relevance)

  • Griffiths, Kieran
  • Griffin, John
  • Desai, Aamod V.
  • Seymour, Valerie Ruth
  • Griffin, John M.
  • Morris, Russell E.
  • Whewell, Tommy
  • Armstrong, A. Robert
  • Griffin, J. M.
  • Cervini, L.
  • Cross, C.
  • Shah, Sayed
  • Hardy, John George
  • Mort, Richard
  • Robinson, Bj
  • Firlak, Melike
  • Geier, Michael J.
  • Westcott, Stephen A.
  • Lee, Graham M.
  • Decken, Andreas
  • Oneill, Taryn
  • Webb, Michael I.
  • Vogels, Christopher M.
  • Bowes, Eric G.
  • Flewelling, Andrew
  • Gray, Christopher A.
  • Li, Haoxin
OrganizationsLocationPeople

article

Long-Term Solar Energy Storage under Ambient Conditions in a MOF-Based Solid–Solid Phase-Change Material

  • Griffiths, Kieran
  • Griffin, John
  • Halcovitch, Nathan Ross
Abstract

This paper demonstrates a metal−organic framework (MOF) containing photoswitches within the pores as a hybrid solar thermal fuel (STF) and solid−solid phase-change material (ss-PCM). A series of azobenzene-loaded MOFs were synthesized with the general formula Zn2(BDC)2(DABCO)(AB)x<br/>(BDC = 1,4-benzenedicarboxylate, DABCO = 1,4-<br/>diazabicyclo[2.2.2]octane, AB = azobenzene, where x = 1.0, 0.9,<br/>0.5, 0.3), herein named 1⊃AB1.0, 1⊃AB0.9, 1⊃AB0.5, and 1⊃AB0.3 respectively. X-ray powder diffraction, solid-state NMR, and density functional theory calculations were used to explore in detail the structural changes of the host framework that take place upon loading with the AB guest molecules. Differential scanning calorimetry measurements reveal a reversible phase change, which is absent from the evacuated framework. Upon irradiation with 365 nm light, 40% of the AB guests converted from the trans to the higher-energy cis isomeric form in 1⊃AB1.0. The energy stored within the metastable cis isomers is released upon heating and balances the endotherm associated with the phase transition.<br/>However, the exotherm associated with the phase transition is retained upon cooling, resulting in a net energy release over a full heating−cooling cycle. The maximum energy density is observed for the fully loaded composite 1⊃AB1.0, which releases 28.9 J g−1.<br/>In addition, the cis-AB guests in this composite showed negligible thermal reconversion during 4 months at ambient temperature, with an estimated energy storage half-life of 4.5 years. Further development of MOF-based STF-ss-PCMs could lead to applications for solar energy conversion and storage, and thermal management.

Topics
  • density
  • impedance spectroscopy
  • pore
  • energy density
  • phase
  • theory
  • composite
  • phase transition
  • density functional theory
  • differential scanning calorimetry
  • Nuclear Magnetic Resonance spectroscopy
  • chemical ionisation