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
To settle the unsatisfying efficiency and insufficient light harvesting ability of photocatalysts, we report on the development of Er/Yb-codoped BiOBr (BiOBr:Er/Yb) microparticles that were synthesized by a rational high-temperature solid-state reaction method. The prepared microcrystals exhibit high visible upconversion (UC) emissions with maximum intensities at = 0.01 when excited by a 980 nm laser. Remarkably, the corresponding UC emission process is attributed to a two-photon absorption route. Furthermore, the photocatalytic activities of as-synthesized compounds were further evaluated through analyzing the visible-near-infrared light-triggered tetracycline degradation. Compared with BiOBr:Er microparticles, BiOBr:Er/Yb microparticles present superior photocatalytic properties and the optimal status is achieved when = 0.05, in which h, ·O, and ·OH active species contribute to the photocatalytic mechanism. Additionally, the designed microparticles exhibit better photocatalytic abilities than previously reported photocatalysts (i.e., TiO, SnO) upon full-spectrum light irradiation. These results reveal that Yb codoping is able to not only enhance the UC emission properties of BiOBr:Er microparticles but also reinforce their photocatalytic activities. Our findings may put forward a facile strategy to regulate the photodegradation capacity of photcatalysts.
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Source |
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http://dx.doi.org/10.1021/acs.langmuir.2c01769 | DOI Listing |
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