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1,4,5,8-Naphthalene tetracarboxylate dianhydride/g-C(3)N(4) van der Waals heterojunctions exhibit enhanced photochemical H(2)O(2) production and antimicrobial activity

Organic semiconductors, including graphitic carbon nitride (g-C(3)N(4), CN), represent an important class of materials for the development of novel antimicrobial or biomedical technologies. Of principal interest is the ability of these materials to catalyze the reduction of elemental oxygen to gener...

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Detalles Bibliográficos
Autores principales: Thurston, John H., Vitale-Sullivan, Molly, Koshkimbayeva, Azhar, Smith, Tyler R., Cornell, Kenneth A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9043264/
https://www.ncbi.nlm.nih.gov/pubmed/35493168
http://dx.doi.org/10.1039/d1ra07473c
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author Thurston, John H.
Vitale-Sullivan, Molly
Koshkimbayeva, Azhar
Smith, Tyler R.
Cornell, Kenneth A.
author_facet Thurston, John H.
Vitale-Sullivan, Molly
Koshkimbayeva, Azhar
Smith, Tyler R.
Cornell, Kenneth A.
author_sort Thurston, John H.
collection PubMed
description Organic semiconductors, including graphitic carbon nitride (g-C(3)N(4), CN), represent an important class of materials for the development of novel antimicrobial or biomedical technologies. Of principal interest is the ability of these materials to catalyze the reduction of elemental oxygen to generate reactive oxygen species (ROS), including hydrogen peroxide (H(2)O(2)). Here, we describe the fabrication of photoactive van der Waals heterojunctions incorporating 1,4,5,8-naphthalene tetracarboxylic dianhydride (NTCDA) and CN. The composite heterojunction systems were characterized by a combination of physical (TEM, SEM, pXRD), spectroscopic (FT-IR, XPS, DRUV, photoluminescence, TCSPC) and kinetic experiments. Electronic interactions between the two components of the heterojunction increase the rate of photochemical production of H(2)O(2) from elemental oxygen by 410%, relative to samples of pure CN. Mechanistic analysis reveals that interaction of NTCDA with the surface of CN modifies the mechanism of H(2)O(2) formation in the heterojunction photocatalysts. The photochemical production of H(2)O(2) by irradiation of the most active heterojunction composition is sufficient to reduce the viability of E. coli O157:H7, S. aureus and Ps. aeruginosa PAO1 by 99%. Importantly, H(2)O(2) production by the NTCDA/CN heterojunctions suppresses Ps. aeruginosa biofilm formation, even at light exposure doses that had a lesser impact on overall planktonic cell growth.
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spelling pubmed-90432642022-04-28 1,4,5,8-Naphthalene tetracarboxylate dianhydride/g-C(3)N(4) van der Waals heterojunctions exhibit enhanced photochemical H(2)O(2) production and antimicrobial activity Thurston, John H. Vitale-Sullivan, Molly Koshkimbayeva, Azhar Smith, Tyler R. Cornell, Kenneth A. RSC Adv Chemistry Organic semiconductors, including graphitic carbon nitride (g-C(3)N(4), CN), represent an important class of materials for the development of novel antimicrobial or biomedical technologies. Of principal interest is the ability of these materials to catalyze the reduction of elemental oxygen to generate reactive oxygen species (ROS), including hydrogen peroxide (H(2)O(2)). Here, we describe the fabrication of photoactive van der Waals heterojunctions incorporating 1,4,5,8-naphthalene tetracarboxylic dianhydride (NTCDA) and CN. The composite heterojunction systems were characterized by a combination of physical (TEM, SEM, pXRD), spectroscopic (FT-IR, XPS, DRUV, photoluminescence, TCSPC) and kinetic experiments. Electronic interactions between the two components of the heterojunction increase the rate of photochemical production of H(2)O(2) from elemental oxygen by 410%, relative to samples of pure CN. Mechanistic analysis reveals that interaction of NTCDA with the surface of CN modifies the mechanism of H(2)O(2) formation in the heterojunction photocatalysts. The photochemical production of H(2)O(2) by irradiation of the most active heterojunction composition is sufficient to reduce the viability of E. coli O157:H7, S. aureus and Ps. aeruginosa PAO1 by 99%. Importantly, H(2)O(2) production by the NTCDA/CN heterojunctions suppresses Ps. aeruginosa biofilm formation, even at light exposure doses that had a lesser impact on overall planktonic cell growth. The Royal Society of Chemistry 2021-11-03 /pmc/articles/PMC9043264/ /pubmed/35493168 http://dx.doi.org/10.1039/d1ra07473c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Thurston, John H.
Vitale-Sullivan, Molly
Koshkimbayeva, Azhar
Smith, Tyler R.
Cornell, Kenneth A.
1,4,5,8-Naphthalene tetracarboxylate dianhydride/g-C(3)N(4) van der Waals heterojunctions exhibit enhanced photochemical H(2)O(2) production and antimicrobial activity
title 1,4,5,8-Naphthalene tetracarboxylate dianhydride/g-C(3)N(4) van der Waals heterojunctions exhibit enhanced photochemical H(2)O(2) production and antimicrobial activity
title_full 1,4,5,8-Naphthalene tetracarboxylate dianhydride/g-C(3)N(4) van der Waals heterojunctions exhibit enhanced photochemical H(2)O(2) production and antimicrobial activity
title_fullStr 1,4,5,8-Naphthalene tetracarboxylate dianhydride/g-C(3)N(4) van der Waals heterojunctions exhibit enhanced photochemical H(2)O(2) production and antimicrobial activity
title_full_unstemmed 1,4,5,8-Naphthalene tetracarboxylate dianhydride/g-C(3)N(4) van der Waals heterojunctions exhibit enhanced photochemical H(2)O(2) production and antimicrobial activity
title_short 1,4,5,8-Naphthalene tetracarboxylate dianhydride/g-C(3)N(4) van der Waals heterojunctions exhibit enhanced photochemical H(2)O(2) production and antimicrobial activity
title_sort 1,4,5,8-naphthalene tetracarboxylate dianhydride/g-c(3)n(4) van der waals heterojunctions exhibit enhanced photochemical h(2)o(2) production and antimicrobial activity
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9043264/
https://www.ncbi.nlm.nih.gov/pubmed/35493168
http://dx.doi.org/10.1039/d1ra07473c
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