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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Two novel inorganic-organic hybrid zinc phosphites, namely, [Zn(1,2-bimb)(HPO)] (1) and [Zn(1,4-bmimb)(HPO)] (2), (1,2-bimb = 1,2-bis(imidazol-1ylmethyl)benzene; 1,4-bmimb = 1,4-bis((2-methyl-1-imidazol-1yl)methyl)benzene) were synthesized for the first time by hydrothermal reaction. Compound 1 generates a three-dimensional (3D) pillared-layer structure with a 2-nodal 3,4-connected topology. While compound 2 exhibits a 2D hybrid zinc phosphite sheet with a 3,4-connected topology network. Utilizing compound 1 and compound 2 as templates and NaS as an etching agent, a series of highly efficient ZnO/ZnS photocatalysts were obtained. The optimized 1-160 sample demonstrates the highest evolution rate of 22.6 mmol g h, exceeding the rate of commercial ZnS samples by more than 14.5 times. The remarkable photocatalytic activity should be attributed to the unique heterojunction structure which shortens the free path of charge carriers and enhances the charge separation efficiency. This work provides a facile strategy for preparing photocatalysts with efficient photocatalytic hydrogen production derived from inorganic-organic hybrid material.
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Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9047063 | PMC |
http://dx.doi.org/10.1039/c9ra06919d | DOI Listing |