Improved solar-driven photocatalytic performance of highly crystalline hydrogenated TiO₂ nanofibers with core-shell structure |
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Author: | Wu, Ming-Chung1,2,3; Chen, Ching-Hsiang4; Huang, Wei-Kang1; |
Organizations: |
1Department of Chemical and Materials Engineering, Chang Gung University, Taoyuan 33302, Taiwan 2Center for Reliability Sciences & Technologies, Chang Gung University, Taoyuan 33302, Taiwan 3Division of Neonatology, Department of Pediatrics, Chang Gung Memorial Hospital, Taoyuan 33305, Taiwan
4Sustainable Energy Development Center, National Taiwan University of Science and Technology, Taipei 10607, Taiwan
5Department of Materials Science and Engineering, National Taiwan University, Taipei 10617, Taiwan 6Department of Chemical and Materials Engineering, National Central University, Taoyuan 32001, Taiwan 7Research Center for Applied Science, Academia Sinica, Taipei 11529, Taiwan 8Microelectronics and Materials Physics Laboratories, Department of Electrical Engineering, University of Oulu, FI-90570 Oulu, Finland |
Format: | article |
Version: | published version |
Access: | open |
Online Access: | PDF Full Text (PDF, 1.8 MB) |
Persistent link: | http://urn.fi/urn:nbn:fi-fe201703102080 |
Language: | English |
Published: |
Springer Nature,
2017
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Publish Date: | 2017-03-10 |
Description: |
AbstractHydrogenated titanium dioxide has attracted intensive research interests in pollutant removal applications due to its high photocatalytic activity. Herein, we demonstrate hydrogenated TiO₂ nanofibers (H:TiO₂ NFs) with a core-shell structure prepared by the hydrothermal synthesis and subsequent heat treatment in hydrogen flow. H:TiO₂ NFs has excellent solar light absorption and photogenerated charge formation behavior as confirmed by optical absorbance, photo-Kelvin force probe microscopy and photoinduced charge carrier dynamics analyses. Photodegradation of various organic dyes such as methyl orange, rhodamine 6G and brilliant green is shown to take place with significantly higher rates on our novel catalyst than on pristine TiO₂ nanofibers and commercial nanoparticle based photocatalytic materials, which is attributed to surface defects (oxygen vacancy and Ti³⁺ interstitial defect) on the hydrogen treated surface. We propose three properties/mechanisms responsible for the enhanced photocatalytic activity, which are: (1) improved absorbance allowing for increased exciton generation, (2) highly crystalline anatase TiO₂ that promotes fast charge transport rate, and (3) decreased charge recombination caused by the nanoscopic Schottky junctions at the interface of pristine core and hydrogenated shell thus promoting long-life surface charges. The developed H:TiO₂ NFs can be helpful for future high performance photocatalysts in environmental applications. see all
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Series: |
Scientific reports |
ISSN: | 2045-2322 |
ISSN-E: | 2045-2322 |
ISSN-L: | 2045-2322 |
Issue: | 7 |
Article number: | 40896 |
DOI: | 10.1038/srep40896 |
OADOI: | https://oadoi.org/10.1038/srep40896 |
Type of Publication: |
A1 Journal article – refereed |
Field of Science: |
221 Nanotechnology 213 Electronic, automation and communications engineering, electronics |
Subjects: | |
Funding: |
The authors appreciate Dr. Ming-Tao Lee group (BL-13A1) at National Synchrotron Radiation Research Centre and Prof. Hsiu-Po Kuo at Chang Gung University for useful discussion and Miss Y.-M. Chang at Instrumentation Centre of National Tsing Hua University for the TEM microstructure analysis. The authors also acknowledge the financial support of the Ministry of Science and Technology, Taiwan (MOST 105-2221-E-182-011, MOST 105-2632-E-182-001, and MOST 105-3113-E-002-010) and the financial support of Chang Gung Memorial Hospital, Linkou, Taiwan (CMRPD2F0161 and BMRPC74). |
Copyright information: |
This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
https://creativecommons.org/licenses/by/4.0/ |