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Electroactive Nanoporous Metal Oxides and Chalcogenides by Chemical Design

Hendon, CH; Butler, KT; Ganose, AM; Román-Leshkov, Y; Scanlon, DO; Ozin, GA; Walsh, A; (2017) Electroactive Nanoporous Metal Oxides and Chalcogenides by Chemical Design. Chemistry of Materials , 29 (8) pp. 3663-3670. 10.1021/acs.chemmater.7b00464. Green open access

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Abstract

The archetypal silica- and aluminosilicate-based zeolite-type materials are renowned for wide-ranging applications in heterogeneous catalysis, gas-separation and ion-exchange. Their compositional space can be expanded to include nanoporous metal chalcogenides, exemplified by germanium and tin sulfides and selenides. By comparison with the properties of bulk metal dichalcogenides and their 2D derivatives, these open-framework analogues may be viewed as three-dimensional semiconductors filled with nanometer voids. Applications exist in a range of molecule size and shape discriminating devices. However, what is the electronic structure of nanoporous metal chalcogenides? Herein, materials modeling is used to describe the properties of a homologous series of nanoporous metal chalcogenides denoted np-MX2, where M = Si, Ge, Sn, Pb, and X = O, S, Se, Te, with Sodalite, LTA and aluminum chromium phosphate-1 structure types. Depending on the choice of metal and anion their properties can be tuned from insulators to semiconductors to metals with additional modification achieved through doping, solid solutions, and inclusion (with fullerene, quantum dots, and hole transport materials). These systems form the basis of a new branch of semiconductor nanochemistry in three dimensions.

Type: Article
Title: Electroactive Nanoporous Metal Oxides and Chalcogenides by Chemical Design
Open access status: An open access version is available from UCL Discovery
DOI: 10.1021/acs.chemmater.7b00464
Publisher version: http://doi.org/10.1021/acs.chemmater.7b00464
Language: English
Additional information: This is an open access article published under a Creative Commons Attribution (CC-BY) License, which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.
UCL classification: UCL
UCL > Provost and Vice Provost Offices > UCL BEAMS
UCL > Provost and Vice Provost Offices > UCL BEAMS > Faculty of Maths and Physical Sciences
UCL > Provost and Vice Provost Offices > UCL BEAMS > Faculty of Maths and Physical Sciences > Dept of Chemistry
URI: https://discovery-pp.ucl.ac.uk/id/eprint/1551447
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