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
Fabrication of efficient photocatalysts with great visible light utilization ability, rapid carriers' separation, and suitable redox potential is essential for improving photocatalytic CO reduction. Herein, flower-like microspheres BiSnO/NiAl-layered double hydroxide (BSO/LDH) heterojunctions were prepared by hydrothermal process for CO reduction. The BiSnO nanoparticles were dispersed on NiAl-LDH nanosheets, with tight contact interface, which facilitated charges transfer and exposing more catalytic active sites. Results of photochemical deposition of metal/metal oxide demonstrated that interfacial charges transfer of the BSO/LDH followed Z-scheme mechanism, endowing more desired redox potential and more efficient carriers separation. The 30%-BSO/LDH showed the highest CO and CH yields of 37.91 and 1.18 μmol g h under visible light irradiation, 3.4 and 2.0 times higher than those from the NiAl-LDH, respectively. The main intermediates during CO reduction were carboxylate (COOH*) and aldehyde group (CHO*), and CO reduction pathways and mechanism were proposed accordingly. This study provided referential strategy for designing efficient heterojunction photocatalysts for CO conversion.
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Source |
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http://dx.doi.org/10.1016/j.jcis.2022.09.017 | DOI Listing |
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