Severity: Warning
Message: file_get_contents(https://...@pubfacts.com&api_key=b8daa3ad693db53b1410957c26c9a51b4908&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 176
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 176
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 250
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3122
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 575
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 489
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 316
Function: require_once
Herein, we report the development of a hydrogenated MoS QD-TiO (HMT) heterojunction as an efficient photocatalytic system via a one-pot hydrothermal reaction followed by hydrogenation. This synthetic strategy facilitates the formation of MoS QDs with an enhanced band gap and a proper heterojunction between them and TiO, which accelerates charge transfer process. Hydrogenation leads to oxygen vacancies in TiO, enhancing the visible light absorption capacity through narrowing its band gap, and sulfur vacancies in MoS, which enhance the active sites for hydrogen adsorption. Due to the band gap reduction of hydrogenated TiO and the band gap enhancement of the MoS QDs, the energy states are rearranged to create a reverse movement of electrons and holes facilitated the charge transfer process which enhance life-time of photo-generated charges. The photocatalyst showed stable, efficient and exceptionally high noble metal free sunlight-induced hydrogen production with a maximum rate of 3.1 mmol g h. The developed synthetic strategy also provides flexibility towards the shape of the MoS, e.g. QDs/single or few layers, on TiO and offers the opportunity to design novel visible light active photocatalysts for different applications.
Download full-text PDF |
Source |
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http://dx.doi.org/10.1039/c7nr06526d | DOI Listing |
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