Please use this identifier to cite or link to this item:
http://hdl.handle.net/10397/101499
| DC Field | Value | Language |
|---|---|---|
| dc.contributor | Department of Applied Biology and Chemical Technology | en_US |
| dc.creator | Zhang, X | en_US |
| dc.creator | Hao, W | en_US |
| dc.creator | Tsang, CS | en_US |
| dc.creator | Liu, M | en_US |
| dc.creator | Hwang, GS | en_US |
| dc.creator | Lee, LYS | en_US |
| dc.date.accessioned | 2023-09-18T07:30:25Z | - |
| dc.date.available | 2023-09-18T07:30:25Z | - |
| dc.identifier.uri | http://hdl.handle.net/10397/101499 | - |
| dc.language.iso | en | en_US |
| dc.publisher | American Chemical Society | en_US |
| dc.rights | © 2019 American Chemical Society | en_US |
| dc.rights | This document is the Accepted Manuscript version of a Published Work that appeared in final form in ACS Applied Energy Materials, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acsaem.9b01790. | en_US |
| dc.subject | Band structure engineering | en_US |
| dc.subject | Oxygen vacancy | en_US |
| dc.subject | Phase transition | en_US |
| dc.subject | Photocatalytic hydrogen evolution | en_US |
| dc.subject | Tungsten oxide | en_US |
| dc.title | Psesudocubic phase tungsten oxide as a photocatalyst for hydrogen evolution reaction | en_US |
| dc.type | Journal/Magazine Article | en_US |
| dc.identifier.spage | 8792 | en_US |
| dc.identifier.epage | 8800 | en_US |
| dc.identifier.volume | 2 | en_US |
| dc.identifier.issue | 12 | en_US |
| dc.identifier.doi | 10.1021/acsaem.9b01790 | en_US |
| dcterms.abstract | Defect and phase engineering can effectively tune the activity of photocatalysts by altering their band structure and active site configuration. Herein, we report the phase-controlled synthesis of tungsten oxide (WO3) nanoplates via a wet-chemical approach. By adjusting the ratio of trioctylphosphine and trioctylphosphine oxide, oxygen vacancies are induced in WO3 at a relatively low temperature, accompanying the crystal structure transition from monoclinic to orthorhombic or pseudocubic phase. The experimental results and DFT calculations reveal that the increased oxygen vacant sites in WO3 lead to the upshift in both conduction band minimum and valence band maximum. The reformed band structure of reduced WO3 samples (WO3-x) enables the photocatalytic hydrogen evolution without cocatalyst at a maximum steady rate of 340 μmol g-1 h-1 under simulated sunlight. Our work demonstrates a simple and effective strategy of introducing oxygen vacancy to WO3 for band structure tuning, which may be further extended to other metal oxide systems. | en_US |
| dcterms.accessRights | open access | en_US |
| dcterms.bibliographicCitation | ACS applied energy materials, 23 Dec. 2019, v. 2, no. 12, p. 8792-8800 | en_US |
| dcterms.isPartOf | ACS applied energy materials | en_US |
| dcterms.issued | 2019-12-23 | - |
| dc.identifier.scopus | 2-s2.0-85075551720 | - |
| dc.identifier.eissn | 2574-0962 | en_US |
| dc.description.validate | 202308 bckw | en_US |
| dc.description.oa | Accepted Manuscript | en_US |
| dc.identifier.FolderNumber | ABCT-0326 | - |
| dc.description.fundingSource | Others | en_US |
| dc.description.fundingText | The Innovation and Technology Commission of Hong Kong; The Hong Kong Polytechnic University | en_US |
| dc.description.pubStatus | Published | en_US |
| dc.identifier.OPUS | 20616201 | - |
| dc.description.oaCategory | Green (AAM) | en_US |
| Appears in Collections: | Journal/Magazine Article | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| Zhang_Pseudocubic_Phase_Tungsten.pdf | Pre-Published version | 2.17 MB | Adobe PDF | View/Open |
Page views
64
Citations as of Apr 14, 2025
Downloads
41
Citations as of Apr 14, 2025
SCOPUSTM
Citations
31
Citations as of Dec 19, 2025
WEB OF SCIENCETM
Citations
27
Citations as of Oct 10, 2024
Google ScholarTM
Check
Altmetric
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.



