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Influence of the Ion Coordination Number on Cation Exchange Reactions with Copper Telluride Nanocrystals
[Image: see text] Cu(2–x)Te nanocubes were used as starting seeds to access metal telluride nanocrystals by cation exchanges at room temperature. The coordination number of the entering cations was found to play an important role in dictating the reaction pathways. The exchanges with tetrahedrally c...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5736242/ https://www.ncbi.nlm.nih.gov/pubmed/27177274 http://dx.doi.org/10.1021/jacs.6b02830 |
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author | Tu, Renyong Xie, Yi Bertoni, Giovanni Lak, Aidin Gaspari, Roberto Rapallo, Arnaldo Cavalli, Andrea Trizio, Luca De Manna, Liberato |
author_facet | Tu, Renyong Xie, Yi Bertoni, Giovanni Lak, Aidin Gaspari, Roberto Rapallo, Arnaldo Cavalli, Andrea Trizio, Luca De Manna, Liberato |
author_sort | Tu, Renyong |
collection | PubMed |
description | [Image: see text] Cu(2–x)Te nanocubes were used as starting seeds to access metal telluride nanocrystals by cation exchanges at room temperature. The coordination number of the entering cations was found to play an important role in dictating the reaction pathways. The exchanges with tetrahedrally coordinated cations (i.e., with coordination number 4), such as Cd(2+) or Hg(2+), yielded monocrystalline CdTe or HgTe nanocrystals with Cu(2–x)Te/CdTe or Cu(2–x)Te/HgTe Janus-like heterostructures as intermediates. The formation of Janus-like architectures was attributed to the high diffusion rate of the relatively small tetrahedrally coordinated cations, which could rapidly diffuse in the Cu(2–x)Te NCs and nucleate the CdTe (or HgTe) phase in a preferred region of the host structure. Also, with both Cd(2+) and Hg(2+) ions the exchange led to wurtzite CdTe and HgTe phases rather than the more stable zinc-blende ones, indicating that the anion framework of the starting Cu(2–x)Te particles could be more easily deformed to match the anion framework of the metastable wurtzite structures. As hexagonal HgTe had never been reported to date, this represents another case of metastable new phases that can only be accessed by cation exchange. On the other hand, the exchanges involving octahedrally coordinated ions (i.e., with coordination number 6), such as Pb(2+) or Sn(2+), yielded rock-salt polycrystalline PbTe or SnTe nanocrystals with Cu(2–x)Te@PbTe or Cu(2–x)Te@SnTe core@shell architectures at the early stages of the exchange process. In this case, the octahedrally coordinated ions are probably too large to diffuse easily through the Cu(2–x)Te structure: their limited diffusion rate restricts their initial reaction to the surface of the nanocrystals, where cation exchange is initiated unselectively, leading to core@shell architectures. Interestingly, these heterostructures were found to be metastable as they evolved to stable Janus-like architectures if annealed at 200 °C under vacuum. |
format | Online Article Text |
id | pubmed-5736242 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-57362422017-12-26 Influence of the Ion Coordination Number on Cation Exchange Reactions with Copper Telluride Nanocrystals Tu, Renyong Xie, Yi Bertoni, Giovanni Lak, Aidin Gaspari, Roberto Rapallo, Arnaldo Cavalli, Andrea Trizio, Luca De Manna, Liberato J Am Chem Soc [Image: see text] Cu(2–x)Te nanocubes were used as starting seeds to access metal telluride nanocrystals by cation exchanges at room temperature. The coordination number of the entering cations was found to play an important role in dictating the reaction pathways. The exchanges with tetrahedrally coordinated cations (i.e., with coordination number 4), such as Cd(2+) or Hg(2+), yielded monocrystalline CdTe or HgTe nanocrystals with Cu(2–x)Te/CdTe or Cu(2–x)Te/HgTe Janus-like heterostructures as intermediates. The formation of Janus-like architectures was attributed to the high diffusion rate of the relatively small tetrahedrally coordinated cations, which could rapidly diffuse in the Cu(2–x)Te NCs and nucleate the CdTe (or HgTe) phase in a preferred region of the host structure. Also, with both Cd(2+) and Hg(2+) ions the exchange led to wurtzite CdTe and HgTe phases rather than the more stable zinc-blende ones, indicating that the anion framework of the starting Cu(2–x)Te particles could be more easily deformed to match the anion framework of the metastable wurtzite structures. As hexagonal HgTe had never been reported to date, this represents another case of metastable new phases that can only be accessed by cation exchange. On the other hand, the exchanges involving octahedrally coordinated ions (i.e., with coordination number 6), such as Pb(2+) or Sn(2+), yielded rock-salt polycrystalline PbTe or SnTe nanocrystals with Cu(2–x)Te@PbTe or Cu(2–x)Te@SnTe core@shell architectures at the early stages of the exchange process. In this case, the octahedrally coordinated ions are probably too large to diffuse easily through the Cu(2–x)Te structure: their limited diffusion rate restricts their initial reaction to the surface of the nanocrystals, where cation exchange is initiated unselectively, leading to core@shell architectures. Interestingly, these heterostructures were found to be metastable as they evolved to stable Janus-like architectures if annealed at 200 °C under vacuum. American Chemical Society 2016-05-13 2016-06-08 /pmc/articles/PMC5736242/ /pubmed/27177274 http://dx.doi.org/10.1021/jacs.6b02830 Text en Copyright © 2016 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Tu, Renyong Xie, Yi Bertoni, Giovanni Lak, Aidin Gaspari, Roberto Rapallo, Arnaldo Cavalli, Andrea Trizio, Luca De Manna, Liberato Influence of the Ion Coordination Number on Cation Exchange Reactions with Copper Telluride Nanocrystals |
title | Influence
of the Ion Coordination Number on Cation
Exchange Reactions with Copper Telluride Nanocrystals |
title_full | Influence
of the Ion Coordination Number on Cation
Exchange Reactions with Copper Telluride Nanocrystals |
title_fullStr | Influence
of the Ion Coordination Number on Cation
Exchange Reactions with Copper Telluride Nanocrystals |
title_full_unstemmed | Influence
of the Ion Coordination Number on Cation
Exchange Reactions with Copper Telluride Nanocrystals |
title_short | Influence
of the Ion Coordination Number on Cation
Exchange Reactions with Copper Telluride Nanocrystals |
title_sort | influence
of the ion coordination number on cation
exchange reactions with copper telluride nanocrystals |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5736242/ https://www.ncbi.nlm.nih.gov/pubmed/27177274 http://dx.doi.org/10.1021/jacs.6b02830 |
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