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: 197
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 197
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 271
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3165
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 597
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 511
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 317
Function: require_once
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Organic room temperature phosphorescence (RTP) materials, with long lifetime, large Stokes shift, and high signal-to-noise ratio, have great potential in numerous fields. And now, the host-guest-doped systems have become an effective approach for facilitating RTP, regardless of the still unclear inherent mechanism. In this work, a series of host-guest-doped RTP materials were constructed, and based on experimental results, the "strong assisting weak" effect was proposed. That is, the host with strong spin-orbit coupling (SOC) effect can effectively enhance the phosphorescence of the guest with weak intersystem crossing (ISC), while maintaining the guest's relatively long lifetime. With 4-dimethylaminopyridine (DMAP) as the host and naphthalene (NL) as the guest, the long RTP lifetime of 1.79 s could be achieved, which is obviously longer than 0.5 s of NL@ polymethyl methacrylate (PMMA). Triplet-triplet energy transfer (TTET) process from the dark triplet excitons of DMAP to NL was found to play the key role in triggering RTP of NL. These findings deepen our understandings of RTP mechanisms and provide practical guidance for the creation of highly efficient and long-lived RTP materials.
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http://dx.doi.org/10.1002/anie.202508587 | DOI Listing |