A facile fynthesis of ZnS nanostructures via liquid-solid reactions

dc.contributor.authorWeerachon Phoohinkong
dc.contributor.authorThitinat Sukonket
dc.contributor.authorUdomsak Kitthawee
dc.date.accessioned2025-03-10T07:37:41Z
dc.date.available2025-03-10T07:37:41Z
dc.date.issued2014
dc.description.abstractZinc sulfide (ZnS) nanostructures are important materials for many technologies such as sensors, infrared windows, transistors, LED displays, and solar cells. However, many methods of synthesizing ZnS nanostructures are complex and require expensive equipment. In this study, a liquid-solid chemical reaction without surfactant was used to synthesize ZnS at room temperature. In addition, commercial grade zinc oxide (ZnO) particles were used as a precursor. The effect of the addition of acids and inorganic salts were investigated. The products were characterized by field emission scanning electron microscopy (FESEM) coupled with energy-dispersive X-ray spectroscopy (EDX), and transmission electron microscopy (TEM). The results show that the nanoparticles of ZnS were obtained in hydrochloric acid and acetic acid addition. The diameters were in the range of 10 to 20 nm and 50 to 100 nm, respectively. In the case of a sodium chloride salt addition, a ZnS structure was obtained with a particle size of approximately 5 nm and a flake-like morphology. © (2014) Trans Tech Publications, Switzerland.
dc.identifier.citationAdvanced Materials Research
dc.identifier.doi10.4028/www.scientific.net/AMR.979.184
dc.identifier.isbn978-303835145-0
dc.identifier.issn10226680
dc.identifier.scopus2-s2.0-84904196552
dc.identifier.urihttps://repository.dusit.ac.th//handle/123456789/5036
dc.languageEnglish
dc.publisherTrans Tech Publications Ltd
dc.rights.holderScopus
dc.subjectLiquid-solid reaction
dc.subjectZinc sulfide nanostructures
dc.subjectZnS nanoparticle
dc.titleA facile fynthesis of ZnS nanostructures via liquid-solid reactions
dc.typeConference paper
mods.location.urlhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84904196552&doi=10.4028%2fwww.scientific.net%2fAMR.979.184&partnerID=40&md5=eb2dd0e5bd7070da89ece9dba578b934
oaire.citation.endPage187
oaire.citation.startPage184
oaire.citation.volume979
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