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
In this work, a novel plasmonic ternary Bi/Bismuth oxycarbonate/Zinc bismuth oxide (Bi-BiOCO-ZnBiO) is synthesized synergistically by a one-step hydrothermal method. The results show that the metallic Bi spheres and ZnBiO nanoparticles are uniformly distributed on the surface of flower-like BiOCO layer. Compared with the bare ZnBiO and Bi-BiOCO, the ternary Bi-BiOCO-ZnBiO heterojunction displays a significantly improved solar energy harvesting efficiency and enhanced photocatalytic degradation activity for environmental organic pollutants. The degradation efficiency of organics reaches to 98.4% under simulated solar light illumination. The degradation kinetics indicates that the photocatalytic reaction rate constant of ternary system is about 4.4 and 29.5 times higher than that of pure ZnBiO and Bi-BiOCO, respectively. Moreover, O and h are the main active species in the photodegradation reaction. The improvement of the photocatalytic activity of the composites is attributed to the synergistic effect of ternary heterostructure and surface plasmon resonance (SPR), which promotes charge transfer and effectively inhibits the recombination of photogenerated carriers.
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Source |
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http://dx.doi.org/10.1016/j.jcis.2022.02.026 | DOI Listing |
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