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: 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
Hollow frame structures are of special interest in the realm of catalysis since they hold only ridges and hollow interiors, enabling the accessibility of active sites to the most extent. Herein, we prepared Pd-Pt hollow frame structures composed of double-shell cubes linked by body diagonals as an efficient catalyst toward the oxygen reduction reaction (ORR), inspired by the 4D analogue of a cube, denoted as a tesseract. The etching process involves the selective removal of Pd atoms and the subsequent rearrangement of the remaining Pd and Pt atoms. The successful preparation of Pd-Pt tesseracts via etching lies in the selection of Pd/Pt ratio in the initial Pd-Pt nanocubes. With various ratios of Pd-Pt nanocubes as templates, we obtained Pd-Pt octapods, tesseracts, and nanoframes, respectively. During the ORR, Pd-Pt tesseracts exhibited the highest mass activity of 1.86 A mg among these Pd-Pt nanocrystals. On the basis of mechanistic studies, the high activity of Pd-Pt tesseracts derived from the optimal oxygen adsorption energy due to the facet effect and composition effect.
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Source |
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http://dx.doi.org/10.1021/jacs.0c12282 | DOI Listing |
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