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: 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: 1057
Function: getPubMedXML
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3175
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
Single-atom catalysts (SACs) show superior efficiency in electrocatalytic carbon dioxide reduction, a key stage in achieving carbon neutrality. Atomically dispersed single-metal sites of SACs are invariably in a positive valence state; namely, they are positively charged single-metal sites (PCSSs). The PCSS catalysts generally possess a distinctive and asymmetric electronic structure, which enables the activation of linear carbon dioxide molecules and stabilizes miscellaneous intermediates during electrocatalysis. Herein, this review summarizes the manner in which the coordination environment, neighboring atoms or groups, and the interaction with the substrate modulate the distinctive electronic properties of PCSSs. Additionally, we overview the recently reported theoretical and experimental advances in terms of structure-performance relationship. Furthermore, we emphasize the previously underappreciated durability of positively charged single-metal sites in CO reduction. Finally, we discuss several pending issues and potential breakthroughs of PCSSs for CO reduction.
Download full-text PDF |
Source |
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http://dx.doi.org/10.1021/acsami.4c21988 | DOI Listing |
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