Ag2S nanoparticles anchored on P-doped g-C3N4: a novel 0D/2D p-n 2 heterojunction for superior photocatalytic inactivation of 3 multidrug-resistant E. coli

Photocatalytic inactivation has been proved to be an effective strategy to eliminate pathogenic bacteria in water. Herein, a novel 0D/2D p-n heterojunction of Ag _2 S-anchored P-doped g-C _3 N _4 (Ag _2 S/PCN) were constructed by a simple two-step process coupling one-pot calcination and ultrasonic-...

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Main Authors: Wanshu Yan, Pingping Hu, Yiguo Jiang, Xiuquan Xu, Xianfeng Ma, Mengru Wang, Xinyue Bao
Format: Article
Language:English
Published: IOP Publishing 2022-01-01
Series:Materials Research Express
Subjects:
Online Access:https://doi.org/10.1088/2053-1591/ac8b66
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author Wanshu Yan
Pingping Hu
Yiguo Jiang
Xiuquan Xu
Xianfeng Ma
Mengru Wang
Xinyue Bao
author_facet Wanshu Yan
Pingping Hu
Yiguo Jiang
Xiuquan Xu
Xianfeng Ma
Mengru Wang
Xinyue Bao
author_sort Wanshu Yan
collection DOAJ
description Photocatalytic inactivation has been proved to be an effective strategy to eliminate pathogenic bacteria in water. Herein, a novel 0D/2D p-n heterojunction of Ag _2 S-anchored P-doped g-C _3 N _4 (Ag _2 S/PCN) were constructed by a simple two-step process coupling one-pot calcination and ultrasonic-assisted synthesis. The photocatalytic performance of as-prepared Ag _2 S/PCN composites was investigated by inactivating multidrug-resistant E. coli under visible light irradiation. The results indicated that Ag _2 S/PCN-5 possessed outstanding photocatalytic inactivation activity and superior stability, which could completely inactivate 7.0 log E. coli cells within 60 min. The enhanced photocatalytic activity of Ag _2 S/PCN-5 was mainly attributed to the elevated visible-light response and improved production and transfer of photoexcited charges. In addition, the free radicals trapping experiments results revealed that h ^+ and •O _2 ^− were predominantly responsible for the efficient inactivation activity. Finally, according to the 0D/2D structure and energy band configuration analysis, the enhanced p-n type heterojunction photocatalytic inactivation mechanism of Ag _2 S/PCN was discussed in detail.
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spelling doaj.art-b51a58a0fc6049d0a20a1aacc50b897d2023-08-09T16:16:02ZengIOP PublishingMaterials Research Express2053-15912022-01-019909500110.1088/2053-1591/ac8b66Ag2S nanoparticles anchored on P-doped g-C3N4: a novel 0D/2D p-n 2 heterojunction for superior photocatalytic inactivation of 3 multidrug-resistant E. coliWanshu Yan0Pingping Hu1Yiguo Jiang2Xiuquan Xu3https://orcid.org/0000-0001-9513-0710Xianfeng Ma4Mengru Wang5Xinyue Bao6Wuxi Institute of Mechanical and Electrical Engineering, Jiangsu University , Wuxi, 214121, People’s Republic of ChinaDepartment of Pathology, Zhenjiang Hospital of Chinese Traditional and Western Medicine, Affiliated to Jiangsu University , Zhenjiang, 212000, People’s Republic of ChinaSuzhou Science & Technology Town Hospital, Gusu School, Nanjing Medical University , Suzhou, 215153, People’s Republic of ChinaSchool of Pharmacy, Jiangsu University , Zhenjiang, 212013, People’s Republic of ChinaSchool of Pharmacy, Jiangsu University , Zhenjiang, 212013, People’s Republic of ChinaSchool of Pharmacy, Jiangsu University , Zhenjiang, 212013, People’s Republic of ChinaSchool of Pharmacy, Jiangsu University , Zhenjiang, 212013, People’s Republic of ChinaPhotocatalytic inactivation has been proved to be an effective strategy to eliminate pathogenic bacteria in water. Herein, a novel 0D/2D p-n heterojunction of Ag _2 S-anchored P-doped g-C _3 N _4 (Ag _2 S/PCN) were constructed by a simple two-step process coupling one-pot calcination and ultrasonic-assisted synthesis. The photocatalytic performance of as-prepared Ag _2 S/PCN composites was investigated by inactivating multidrug-resistant E. coli under visible light irradiation. The results indicated that Ag _2 S/PCN-5 possessed outstanding photocatalytic inactivation activity and superior stability, which could completely inactivate 7.0 log E. coli cells within 60 min. The enhanced photocatalytic activity of Ag _2 S/PCN-5 was mainly attributed to the elevated visible-light response and improved production and transfer of photoexcited charges. In addition, the free radicals trapping experiments results revealed that h ^+ and •O _2 ^− were predominantly responsible for the efficient inactivation activity. Finally, according to the 0D/2D structure and energy band configuration analysis, the enhanced p-n type heterojunction photocatalytic inactivation mechanism of Ag _2 S/PCN was discussed in detail.https://doi.org/10.1088/2053-1591/ac8b66g-C3N4P-dopedAg2Sp-n heterojunctionphotocatalytic inactivation
spellingShingle Wanshu Yan
Pingping Hu
Yiguo Jiang
Xiuquan Xu
Xianfeng Ma
Mengru Wang
Xinyue Bao
Ag2S nanoparticles anchored on P-doped g-C3N4: a novel 0D/2D p-n 2 heterojunction for superior photocatalytic inactivation of 3 multidrug-resistant E. coli
Materials Research Express
g-C3N4
P-doped
Ag2S
p-n heterojunction
photocatalytic inactivation
title Ag2S nanoparticles anchored on P-doped g-C3N4: a novel 0D/2D p-n 2 heterojunction for superior photocatalytic inactivation of 3 multidrug-resistant E. coli
title_full Ag2S nanoparticles anchored on P-doped g-C3N4: a novel 0D/2D p-n 2 heterojunction for superior photocatalytic inactivation of 3 multidrug-resistant E. coli
title_fullStr Ag2S nanoparticles anchored on P-doped g-C3N4: a novel 0D/2D p-n 2 heterojunction for superior photocatalytic inactivation of 3 multidrug-resistant E. coli
title_full_unstemmed Ag2S nanoparticles anchored on P-doped g-C3N4: a novel 0D/2D p-n 2 heterojunction for superior photocatalytic inactivation of 3 multidrug-resistant E. coli
title_short Ag2S nanoparticles anchored on P-doped g-C3N4: a novel 0D/2D p-n 2 heterojunction for superior photocatalytic inactivation of 3 multidrug-resistant E. coli
title_sort ag2s nanoparticles anchored on p doped g c3n4 a novel 0d 2d p n 2 heterojunction for superior photocatalytic inactivation of 3 multidrug resistant e coli
topic g-C3N4
P-doped
Ag2S
p-n heterojunction
photocatalytic inactivation
url https://doi.org/10.1088/2053-1591/ac8b66
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