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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Single atom and nanocluster catalysts are extensively investigated in heterogeneous catalysis due to their high catalytic activity and atomic utilization, while their coexisting properties and potentially synergistic effect are yet to be clarified. Herein, we construct three systems of atomic-scale catalysts (xNi/MoTiAlC, x = 0.5, 1, and 1.5) for bio-ethanol reforming, which correspond to single atoms, single atoms mixed with nanoclusters, and nanoclusters. The respective hydrogen utilization efficiency of mixed-form catalyst increases by 43.7% and 29.3% compared to single atom and nanocluster catalysts. Results demonstrate that the adjacent Ni single atom facilitates electron transfer from MoTiAlC to Ni-Mo interface and raises the d-band center, thus enhancing bio-ethanol adsorption and activation; while the existence of Ni nanoclusters contributes to lowering the energy barriers of CHCHO* dehydrogenation. The catalytically active sites are Ni-Mo alloyed single atoms with adjacent Ni nanoclusters. This work provides new implications for highly activated catalytic site construction and advanced catalyst design.
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Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12033288 | PMC |
http://dx.doi.org/10.1038/s41467-025-59127-0 | DOI Listing |