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
An reduction technique consisting of chemisorption of 1,3,5,7-tetramethylcyclotetrasiloxane (TMCTS) and subsequent reaction with HAuCl has been developed for depositing Au nanoparticles (NPs) uniformly in the depth direction of a mesoporous TiO nanocrystalline film (Au/TMCTS/mp-TiO). The TMCTS monolayer is further converted into silicon oxide by heating in the air (Au/SiO/mp-TiO). In the absorption spectra of Au/SiO/mp-TiO prepared at varying HAuCl concentrations (), the localized surface plasmon resonance (LSPR) band of Au NPs significantly broadens ≈ 1.22 mM at 546 nm to be split into two peaks around 500 and 700 nm at ≥ 2.43 mM, whereas such a phenomenon is not observed for the usual Au NP-loaded TiO particles. Three-dimensional-finite difference time domain simulations showed that the unique optical property of Au/SiO/mp-TiO stems from the effective LSPR coupling of very close Au NPs and partial fusions in the nanospaces of mp-TiO. Further, the optical hot spots in Au/TMCTS/mp-TiO as well as Au/SiO/mp-TiO generate an intense local electric field giving increase to a great enhancement of the absorption in the infrared spectrum of the TMCTS monolayer on mp-TiO.
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Source |
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http://dx.doi.org/10.1021/acs.langmuir.0c03184 | DOI Listing |
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