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dc.contributor.authorWang, A.
dc.contributor.authorWang, W.
dc.contributor.authorChen, Jiayi
dc.contributor.authorMao, Rundong
dc.contributor.authorPang, Yingping
dc.contributor.authorLi, Y.
dc.contributor.authorChen, Wei
dc.contributor.authorChen, Dechao
dc.contributor.authorHao, D.
dc.contributor.authorNi, B.J.
dc.contributor.authorSaunders, M.
dc.contributor.authorJia, Guohua
dc.date.accessioned2023-03-15T06:54:53Z
dc.date.available2023-03-15T06:54:53Z
dc.date.issued2020
dc.identifier.citationWang, A. and Wang, W. and Chen, J. and Mao, R. and Pang, Y. and Li, Y. and Chen, W. et al. 2020. Dominant Polar Surfaces of Colloidal II-VI Wurtzite Semiconductor Nanocrystals Enabled by Cation Exchange. Journal of Physical Chemistry Letters. 11 (13): pp. 4990-4997.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/90989
dc.identifier.doi10.1021/acs.jpclett.0c01372
dc.description.abstract

Polar surfaces of ionic crystals are of growing technological importance, with implications for the efficiency of photocatalysts, gas sensors, and electronic devices. The creation of ionic nanocrystals with high percentages of polar surfaces is an option for improving their efficiency in the aforementioned applications but is hard to accomplish because they are less thermodynamically stable and prone to vanish during the growth process. Herein, we develop a strategy that is capable of producing polar surface-dominated II-VI semiconductor nanocrystals, including ZnS and CdS, from copper sulfide hexagonal nanoplates through cation exchange reactions. The obtained wurtzite ZnS hexagonal nanoplates have dominant {002} polar surfaces, occupying up to 97.8% of all surfaces. Density functional theory calculations reveal the polar surfaces can be stabilized by a charge transfer of 0.25 eV/formula from the anion-terminated surface to the cation-terminated surface, which also explains the presence of polar surfaces in the initial Cu1.75S hexagonal nanoplates with cation deficiency prior to cation exchange reactions. Experimental results showed that the HER activity could be boosted by the surface polarization of polar surface-dominated ZnS hexagonal nanoplates. We anticipate this strategy is general and could be used with other systems to prepare nanocrystals with dominant polar surfaces. Furthermore, the availability of colloidal semiconductor nanocrystals with dominant polar surfaces produced through this strategy opens a new avenue for improving their efficiency in catalysis, photocatalysis, gas sensing, and other applications.

dc.languageEnglish
dc.publisherAMER CHEMICAL SOC
dc.relation.sponsoredbyhttp://purl.org/au-research/grants/arc/DE160100589
dc.subjectScience & Technology
dc.subjectPhysical Sciences
dc.subjectTechnology
dc.subjectChemistry, Physical
dc.subjectNanoscience & Nanotechnology
dc.subjectMaterials Science, Multidisciplinary
dc.subjectPhysics, Atomic, Molecular & Chemical
dc.subjectChemistry
dc.subjectScience & Technology - Other Topics
dc.subjectMaterials Science
dc.subjectPhysics
dc.subjectTIO2 SINGLE-CRYSTALS
dc.subjectCDSE NANOCRYSTALS
dc.titleDominant Polar Surfaces of Colloidal II-VI Wurtzite Semiconductor Nanocrystals Enabled by Cation Exchange
dc.typeJournal Article
dcterms.source.volume11
dcterms.source.number13
dcterms.source.startPage4990
dcterms.source.endPage4997
dcterms.source.issn1948-7185
dcterms.source.titleJournal of Physical Chemistry Letters
dc.date.updated2023-03-15T06:54:53Z
curtin.note

This document is the Accepted Manuscript version of a Published Work that appeared in final form in Journal of Physical Chemistry Letters, copyright © American Chemical Society, after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acs.jpclett.0c01372.

curtin.departmentSchool of Molecular and Life Sciences (MLS)
curtin.accessStatusOpen access
curtin.facultyFaculty of Science and Engineering
curtin.contributor.orcidJia, Guohua [0000-0003-1179-2763]
curtin.contributor.orcidChen, Wei [0000-0002-0658-7661]
curtin.contributor.orcidChen, Dechao [0000-0002-9205-2312]
curtin.contributor.researcheridJia, Guohua [C-7325-2013]
dcterms.source.eissn1948-7185
curtin.contributor.scopusauthoridJia, Guohua [56765222900] [7103360294]
curtin.repositoryagreementV3


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