Severity: Warning
Message: file_get_contents(https://...@gmail.com&api_key=61f08fa0b96a73de8c900d749fcb997acc09&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: 1034
Function: getPubMedXML
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3152
Function: GetPubMedArticleOutput_2016
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
The strong adsorption of thiol molecules on gold nanorods (AuNRs) results in localized surface plasmon resonance (LSPR) energy loss chemical interface damping (CID). This study investigated the CID effect induced by thiophenol (TP) adsorption on single AuNRs and the tuning of LSPR properties and chemical interfaces through electrochemical potential manipulation. The potential-dependent LSPR spectrum of bare AuNRs exhibited redshifts and line width broadening owing to the characteristics of capacitive charging, Au oxidation, and oxidation dissolution. However, TP passivation provided stability to the AuNRs from oxidation in an electrochemical environment. Electrochemical potentials induced electron donation and withdrawal, causing changes in the Fermi level of AuNRs at the Au-TP interface, thereby controlling the LSPR spectrum. Additionally, the desorption of TP molecules from the Au surface was electrochemically achieved at the anodic potentials further away from the capacitive charging region, which can be used to tune chemical interfaces and the CID process in single AuNRs.
Download full-text PDF |
Source |
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http://dx.doi.org/10.1021/acs.jpclett.3c01424 | DOI Listing |
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