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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This study presents a new nanoporous TiO/SnO heterojunction for NO gas detection by using a two-step sol-gel process. The unique TiO and SnO nanoheterojunction matrix right on the film surface enables the TiO photocatalyst to absorb minimal UV power (3 μW/cm) and effectively transfer electrons to the SnO conduction band. The sensor detects NO and NO gases down to 4 ppb (response of 0.6%) and 10 ppb (response of 1.3%) at 1 V at room temperature. It also exhibits a fast recovery time (100 ± 40 s at 500 ppb NO), an improved response over a wide relative humidity range (10-60%), and a long lifetime over 30 days. The ultralow UV power required can be easily harvested from sunlight, eliminating the need for UV LEDs. XPS and SEM analyses indicated that the unique nanoporous TiO/SnO structure improves sensing performance, with oxygen vacancies playing a critical role in the NO gas sensing mechanism. This work demonstrated the highly efficient UV catalyst effect in sensors with the surface heterojunction matrix. The low-power ppb-level NO detection is suitable for environmental monitoring and respiratory disease detection.
Download full-text PDF |
Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11891840 | PMC |
http://dx.doi.org/10.1021/acsami.4c19998 | DOI Listing |