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dc.contributor.authorTamang, Sudarsan-
dc.contributor.authorKim, Kyungnam-
dc.contributor.authorChoi, Hyekyoung-
dc.contributor.authorKima, Youngsik-
dc.contributor.authorJeong, Sohee-
dc.date.accessioned2019-09-24T06:44:37Z-
dc.date.available2019-09-24T06:44:37Z-
dc.date.issued2015-
dc.identifier.citationDalton Transactions V. 44, 2015, 16923-16928 pp.en_US
dc.identifier.issn1477-9226-
dc.identifier.urihttps://doi.org/10.1039/C5DT02181B-
dc.identifier.urihttp://dspace.cus.ac.in/jspui/handle/1/6352-
dc.description.abstractIndium antimonide (InSb), a narrow band gap III–V semiconductor is a promising infrared-active material for various optoelectronic applications. Synthetic challenge of colloidal InSb nanocrystals (NCs) lies in the limited choice of precursors. Only a few successful synthetic schemes involving highly toxic stibine (SbH3) or air- and moisture-sensitive metal silylamides (In[N(Si-(Me)3)2]3 or Sb[N(Si-(Me)3)2]3) as the precursor have been reported. We found that commercially available precursors InCl3 and Sb[NMe2]3 directly form highly crystalline colloidal InSb nanocrystals in the presence of a base such as LiN(SiMe3)2 or nBuLi. The mean size of the particles can be controlled by simply changing the activating base. This approach offers a one-pot synthesis of InSb NCs from readily available chemicals without the use of complex organometallic precursorsen_US
dc.language.isoenen_US
dc.titleSynthesis of colloidal InSb nanocrystals via in situ activation of InCl3en_US
dc.typeArticleen_US
dc.identifier.Volume44-
dc.identifier.eissn1477-9234-
Appears in Collections:Sudarsan Tamang

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