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Enhanced Photoelectrochemical Behavior of H-TiO(2) Nanorods Hydrogenated by Controlled and Local Rapid Thermal Annealing

Recently, colored H-doped TiO(2) (H-TiO(2)) has demonstrated enhanced photoelectrochemical (PEC) performance due to its unique crystalline core—disordered shell nanostructures and consequent enhanced conduction behaviors between the core-shell homo-interfaces. Although various hydrogenation approach...

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Autores principales: Wang, Xiaodan, Estradé, Sonia, Lin, Yuanjing, Yu, Feng, Lopez-Conesa, Lluis, Zhou, Hao, Gurram, Sanjeev Kumar, Peiró, Francesca, Fan, Zhiyong, Shen, Hao, Schaefer, Lothar, Braeuer, Guenter, Waag, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5419951/
https://www.ncbi.nlm.nih.gov/pubmed/28482648
http://dx.doi.org/10.1186/s11671-017-2105-x
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author Wang, Xiaodan
Estradé, Sonia
Lin, Yuanjing
Yu, Feng
Lopez-Conesa, Lluis
Zhou, Hao
Gurram, Sanjeev Kumar
Peiró, Francesca
Fan, Zhiyong
Shen, Hao
Schaefer, Lothar
Braeuer, Guenter
Waag, Andreas
author_facet Wang, Xiaodan
Estradé, Sonia
Lin, Yuanjing
Yu, Feng
Lopez-Conesa, Lluis
Zhou, Hao
Gurram, Sanjeev Kumar
Peiró, Francesca
Fan, Zhiyong
Shen, Hao
Schaefer, Lothar
Braeuer, Guenter
Waag, Andreas
author_sort Wang, Xiaodan
collection PubMed
description Recently, colored H-doped TiO(2) (H-TiO(2)) has demonstrated enhanced photoelectrochemical (PEC) performance due to its unique crystalline core—disordered shell nanostructures and consequent enhanced conduction behaviors between the core-shell homo-interfaces. Although various hydrogenation approaches to obtain H-TiO(2) have been developed, such as high temperature hydrogen furnace tube annealing, high pressure hydrogen annealing, hydrogen-plasma assisted reaction, aluminum reduction and electrochemical reduction etc., there is still a lack of a hydrogenation approach in a controlled manner where all processing parameters (temperature, time and hydrogen flux) were precisely controlled in order to improve the PEC performance of H-TiO(2) and understand the physical insight of enhanced PEC performance. Here, we report for the first time a controlled and local rapid thermal annealing (RTA) approach to prepare hydrogenated core-shell H-TiO(2) nanorods grown on F:SnO(2) (FTO) substrate in order to address the degradation issue of FTO in the typical TiO(2) nanorods/FTO system observed in the conventional non-RTA treated approaches. Without the FTO degradation in the RTA approach, we systematically studied the intrinsic relationship between the annealing temperature, structural, optical, and photoelectrochemical properties in order to understand the role of the disordered shell on the improved photoelectrochemical behavior of H-TiO(2) nanorods. Our investigation shows that the improvement of PEC performance could be attributed to (i) band gap narrowing from 3.0 to 2.9 eV; (ii) improved optical absorption in the visible range induced by the three-dimensional (3D) morphology and rough surface of the disordered shell; (iii) increased proper donor density; (iv) enhanced electron–hole separation and injection efficiency due to the formation of disordered shell after hydrogenation. The RTA approach developed here can be used as a suitable hydrogenation process for TiO(2) nanorods/FTO system for important applications such as photocatalysis, hydrogen generation from water splitting and solar energy conversion. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s11671-017-2105-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-54199512017-05-22 Enhanced Photoelectrochemical Behavior of H-TiO(2) Nanorods Hydrogenated by Controlled and Local Rapid Thermal Annealing Wang, Xiaodan Estradé, Sonia Lin, Yuanjing Yu, Feng Lopez-Conesa, Lluis Zhou, Hao Gurram, Sanjeev Kumar Peiró, Francesca Fan, Zhiyong Shen, Hao Schaefer, Lothar Braeuer, Guenter Waag, Andreas Nanoscale Res Lett Nano Express Recently, colored H-doped TiO(2) (H-TiO(2)) has demonstrated enhanced photoelectrochemical (PEC) performance due to its unique crystalline core—disordered shell nanostructures and consequent enhanced conduction behaviors between the core-shell homo-interfaces. Although various hydrogenation approaches to obtain H-TiO(2) have been developed, such as high temperature hydrogen furnace tube annealing, high pressure hydrogen annealing, hydrogen-plasma assisted reaction, aluminum reduction and electrochemical reduction etc., there is still a lack of a hydrogenation approach in a controlled manner where all processing parameters (temperature, time and hydrogen flux) were precisely controlled in order to improve the PEC performance of H-TiO(2) and understand the physical insight of enhanced PEC performance. Here, we report for the first time a controlled and local rapid thermal annealing (RTA) approach to prepare hydrogenated core-shell H-TiO(2) nanorods grown on F:SnO(2) (FTO) substrate in order to address the degradation issue of FTO in the typical TiO(2) nanorods/FTO system observed in the conventional non-RTA treated approaches. Without the FTO degradation in the RTA approach, we systematically studied the intrinsic relationship between the annealing temperature, structural, optical, and photoelectrochemical properties in order to understand the role of the disordered shell on the improved photoelectrochemical behavior of H-TiO(2) nanorods. Our investigation shows that the improvement of PEC performance could be attributed to (i) band gap narrowing from 3.0 to 2.9 eV; (ii) improved optical absorption in the visible range induced by the three-dimensional (3D) morphology and rough surface of the disordered shell; (iii) increased proper donor density; (iv) enhanced electron–hole separation and injection efficiency due to the formation of disordered shell after hydrogenation. The RTA approach developed here can be used as a suitable hydrogenation process for TiO(2) nanorods/FTO system for important applications such as photocatalysis, hydrogen generation from water splitting and solar energy conversion. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s11671-017-2105-x) contains supplementary material, which is available to authorized users. Springer US 2017-05-05 /pmc/articles/PMC5419951/ /pubmed/28482648 http://dx.doi.org/10.1186/s11671-017-2105-x Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Nano Express
Wang, Xiaodan
Estradé, Sonia
Lin, Yuanjing
Yu, Feng
Lopez-Conesa, Lluis
Zhou, Hao
Gurram, Sanjeev Kumar
Peiró, Francesca
Fan, Zhiyong
Shen, Hao
Schaefer, Lothar
Braeuer, Guenter
Waag, Andreas
Enhanced Photoelectrochemical Behavior of H-TiO(2) Nanorods Hydrogenated by Controlled and Local Rapid Thermal Annealing
title Enhanced Photoelectrochemical Behavior of H-TiO(2) Nanorods Hydrogenated by Controlled and Local Rapid Thermal Annealing
title_full Enhanced Photoelectrochemical Behavior of H-TiO(2) Nanorods Hydrogenated by Controlled and Local Rapid Thermal Annealing
title_fullStr Enhanced Photoelectrochemical Behavior of H-TiO(2) Nanorods Hydrogenated by Controlled and Local Rapid Thermal Annealing
title_full_unstemmed Enhanced Photoelectrochemical Behavior of H-TiO(2) Nanorods Hydrogenated by Controlled and Local Rapid Thermal Annealing
title_short Enhanced Photoelectrochemical Behavior of H-TiO(2) Nanorods Hydrogenated by Controlled and Local Rapid Thermal Annealing
title_sort enhanced photoelectrochemical behavior of h-tio(2) nanorods hydrogenated by controlled and local rapid thermal annealing
topic Nano Express
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5419951/
https://www.ncbi.nlm.nih.gov/pubmed/28482648
http://dx.doi.org/10.1186/s11671-017-2105-x
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