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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Although nanoscale Ni-based materials possess exceptional theoretical hydrogen evolution reaction (HER) activity, their synthesis and long-term storage stability remain critical barriers to practical applications. In this study, we propose a controlled oxidation strategy to synthesize amorphous NiO-modified oxidation graphene-encapsulated Ni nanoparticles (Ni@GO) as highly efficient and durable electrocatalysts for alkaline water electrolysis. This strategy integrates a self-assembly confinement effect with a calcination process to fabricate ultrasmall Ni nanocrystals, followed by passivation oxidation to in situ generate a non-uniform amorphous NiO layer on the Ni surface. This approach not only prevents the spontaneous combustion of nanoparticles, thereby significantly enhancing their storage and application stability, but also constructs a locally optimized Ni/Ni synergistic catalytic interface, effectively modulating and balancing the Volmer and Heyrovsky/Tafel reaction pathways, and greatly boosting alkaline HER performance. The synthesized Ni@GO catalyst exhibits an ultra-low overpotential of 60 mV at 10 mA cm in 1 M KOH, as measured on a GCE electrode. Furthermore, it demonstrates an overall water-splitting activity comparable to that of commercial Pt/C and RuO catalysts. Notably, after being stored in ambient air for over 1.5 years, the catalyst retains its excellent electrocatalytic performance. This study presents an efficient, stable, and scalable strategy, providing valuable insights for the design and application of low-cost, high-performance electrocatalysts.
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http://dx.doi.org/10.1016/j.jcis.2025.138283 | DOI Listing |