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: 197
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 197
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 271
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3145
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
Photocatalytic reduction of CO to high-value-added chemicals represents a promising strategy for effective CO utilization, and rationally regulating the electronic structure of the catalyst is the key to enhancing photocatalytic performance. Herein, it is demonstrated that in situ doping of atomic indium into the lattice of the CuMoS catalyst results in remarkable enhancements in photocatalytic CO reduction performance. A record gas product yield of 104.1 µmol·g·h is achieved under visible light irradiation (>420 nm), accompanied by a generation rate of 35.3 µmol·g·h for ethylene. Detailed experimental analyses and density functional theory (DFT) calculations reveal that the low electronegativity of indium atoms induces asymmetric charge redistribution near the doping sites. This effect facilitates the adsorption and dissociation of CO molecules at the charge-enriched Mo sites, as well as the subsequent generation of key intermediates (COCOH) toward ethylene formation. This work advances understanding of the potential mechanism between the electronic structure of the active site and photocatalytic performance, providing valuable insights into fabricating advanced materials for CO conversion into solar fuels.
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Source |
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http://dx.doi.org/10.1002/smll.202500877 | DOI Listing |
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