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Single step combustion synthesis, characterization and photocatalytic application of α-Fe2O3-Bi2S3 heterojunctions for efficient and selective reduction of structurally diverse nitroarenes.

Authors :
Bhoi, Y.P.
Mishra, B.G.
Source :
Chemical Engineering Journal. May2017, Vol. 316, p70-81. 12p.
Publication Year :
2017

Abstract

A series of α-Fe 2 O 3 -Bi 2 S 3 heterojunction materials were prepared by a one-step autocombustion method employing thiourea as fuel. The heterojunction materials were characterized using XRD, UV–Vis-DRS, FTIR, PL, XPS, FESEM, TEM and HRTEM analytical techniques. XRD study indicated presence of rhombohedral α-Fe 2 O 3 and orthorhombic Bi 2 S 3 in the heterojunction materials. The heterojunctions displayed better optical absorption in the visible region and enhanced charge carrier separation characteristics. The oxidation state of the constituent elements on the surface was established from XPS study. IR study showed the characteristic vibrational features of both α-Fe 2 O 3 and Bi 2 S 3 phases. Microscopic studies indicated presence of well dispersed α-Fe 2 O 3 nanorods in a continuous Bi 2 S 3 matrix. The α-Fe 2 O 3 nanorods were typically 30–50 nm in diameter and 120–150 nm in length growing isotopically in different direction from a single nucleation point. The calculated band positions of both components indicated a facile electrons transfer from the conduction band of α-Fe 2 O 3 to Bi 2 S 3 whereas migration of holes occurs in the reverse direction yielding a type-II heterojunction. The α-Fe 2 O 3 -Bi 2 S 3 heterojunctions materials were evaluated as selective and efficient photocatalyst for the hydrogen transfer reduction of nitroarenes under visible light illumination. Structurally diverse nitroarenes could be selectively reduced to the corresponding amines in high yield and purity using α-Fe 2 O 3 -Bi 2 S 3 as photocatalyst. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
13858947
Volume :
316
Database :
Academic Search Index
Journal :
Chemical Engineering Journal
Publication Type :
Academic Journal
Accession number :
121618577
Full Text :
https://doi.org/10.1016/j.cej.2017.01.075