Issue 3, 2016

Heterovalent substitution in anionic and cationic positions of PbS thin-films grown by SILAR method vis-à-vis Fermi energy measured through scanning tunneling spectroscopy

Abstract

We report the growth and characterization of doped-PbS thin-films deposited by a successive ionic layer adsorption and reaction (SILAR) method. Altervalent cation and aliovalent anion substitution by ions of mono- and trivalent elements as dopants have been achieved in the compound semiconductor. The heterovalent elements introduced free carriers into the semiconductors, the nature of which depended on its valency and the ions it substituted into the compound. The effect of such dopants on the Fermi energy of PbS has been followed by scanning tunneling spectroscopy (STS), and was found to have correspondence to the density of states (DOS) of a semiconductor. By locating the conduction and valence band-edges of the pristine and different doped-semiconductors, the STS studies provided a direct evidence of a shift in Fermi energy upon heterovalent cationic and anionic substitution in compound semiconductors.

Graphical abstract: Heterovalent substitution in anionic and cationic positions of PbS thin-films grown by SILAR method vis-à-vis Fermi energy measured through scanning tunneling spectroscopy

Supplementary files

Article information

Article type
Paper
Submitted
25 Nov 2015
Accepted
07 Dec 2015
First published
08 Dec 2015

J. Mater. Chem. C, 2016,4, 551-558

Author version available

Heterovalent substitution in anionic and cationic positions of PbS thin-films grown by SILAR method vis-à-vis Fermi energy measured through scanning tunneling spectroscopy

H. Bhunia, B. Kundu, S. Chatterjee and A. J. Pal, J. Mater. Chem. C, 2016, 4, 551 DOI: 10.1039/C5TC03959B

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements