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
The interaction between metallic nanowires and a metal substrate is investigated by means of transformation optics. This plasmonic system is of particular interest for single molecule detection or nanolasers. By mapping such a plasmonic device onto a metal-insulator-metal infinite structure, its optical response can be fully derived analytically. In this article, the absorption cross-section of a nanowire placed close to a metallic surface is derived within and beyond the quasi-static limit. The system is shown to support several modes characterized by a different angular momentum and whose resonance red-shifts when the nanoparticle approaches the metal substrate. These resonances give rise to a drastic field enhancement (>10(2)) within the narrow gap separating the nanoparticle from the metal surface. The case of a nanowire dimer is also investigated and is closely related to the previous configuration. More physical insights are provided especially with respect to the invisibility dips appearing in the radiative spectrum. Numerical simulations have also been performed to confirm our analytical predictions and determine their range of validity.
Download full-text PDF |
Source |
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http://dx.doi.org/10.1021/nn200438e | DOI Listing |
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