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Understanding charge transport in non-doped pristine and surface passivated hematite (Fe 2 O 3 ) nanorods under front and backside illumination in the context of light induced water splitting.

Authors :
Bassi PS
Xianglin L
Fang Y
Loo JS
Barber J
Wong LH
Source :
Physical chemistry chemical physics : PCCP [Phys Chem Chem Phys] 2016 Nov 09; Vol. 18 (44), pp. 30370-30378.
Publication Year :
2016

Abstract

Hematite (Fe <subscript>2</subscript> O <subscript>3</subscript> ) nanorods on FTO substrates have been proven to be promising photoanodes for solar fuel production but only with high temperature thermal activation which allows diffusion of tin (Sn) ions from FTO, eventually enhancing their conductivity. Hence, there is a trade-off between the conductivity of Fe <subscript>2</subscript> O <subscript>3</subscript> , and the degradation of FTO occurring at high annealing temperatures (>750 °C). Here, we present a comprehensive study on undoped Fe <subscript>2</subscript> O <subscript>3</subscript> nanorods under front and back illumination to find the optimum annealing temperature. Bulk/surface charge transport efficiency analysis demonstrates minimum bulk recombination indicating overall high quality crystalline Fe <subscript>2</subscript> O <subscript>3</subscript> and the preservation of FTO conductivity. Surface recombination is further improved by growing a TiO <subscript>x</subscript> overlayer, which improves the photocurrent density from 0.2 mA cm <superscript>-2</superscript> (backside) to 1.2 mA cm <superscript>-2</superscript> under front side and 0.8 mA cm <superscript>-2</superscript> under backside illumination. It is evident from this study that the performance of undoped and unpassivated hematite nanorods is limited by electron transport, whereas that of doped/passivated hematite nanorods is limited by hole transport.

Details

Language :
English
ISSN :
1463-9084
Volume :
18
Issue :
44
Database :
MEDLINE
Journal :
Physical chemistry chemical physics : PCCP
Publication Type :
Academic Journal
Accession number :
27782252
Full Text :
https://doi.org/10.1039/c6cp05379c