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Insights into Interface Charge Extraction in a Noble-Metal-Free Doped Z-Scheme [email protected] Heterojunction
It is of great significance to thoroughly explore the interface charge extraction and migration in heterojunction systems, which could guide us to synthesize higher-efficiency photocatalytic materials. A novel noble-metal-free doped Z-scheme NiO@BiOCl heterojunction was found in this work. The corre...
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Published in: | Catalysts 2020-01, Vol.10 (9), p.958 |
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creator | Yang, Jun Zhu, Quanxi Xie, Taiping Wang, Jiankang Yuan, Peng Wang, Yajing Liu, Chenglun Xu, Longjun |
description | It is of great significance to thoroughly explore the interface charge extraction and migration in heterojunction systems, which could guide us to synthesize higher-efficiency photocatalytic materials. A novel noble-metal-free doped Z-scheme NiO@BiOCl heterojunction was found in this work. The corresponding heterostructure, interface electron extraction, and electron migration were investigated via first-principles calculation. 5,5′-dimethyl-1-pyrroline-N-oxide (DMPO) spin-trapping electron spin resonance (ESR) and time-resolved photoluminescence (TRPL) tests were implemented to confirm the calculation results, which showed that electrons and holes stayed in the NiO (100) facet and BiOCl (110) facet, respectively. Owing to the large chemical potential of 2.40 V (vs ENHE) for the BiOCl valence-band hole, it possessed super activity to oxidize water into hydroxyl radicals or molecular oxygen. We hope this promising multifunctional photocatalytic material, therefore, NiO@BiOCl can be applied in advanced treatment of organic wastewater and oxygen production from photolysis water. |
doi_str_mv | 10.3390/catal10090958 |
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A novel noble-metal-free doped Z-scheme NiO@BiOCl heterojunction was found in this work. The corresponding heterostructure, interface electron extraction, and electron migration were investigated via first-principles calculation. 5,5′-dimethyl-1-pyrroline-N-oxide (DMPO) spin-trapping electron spin resonance (ESR) and time-resolved photoluminescence (TRPL) tests were implemented to confirm the calculation results, which showed that electrons and holes stayed in the NiO (100) facet and BiOCl (110) facet, respectively. Owing to the large chemical potential of 2.40 V (vs ENHE) for the BiOCl valence-band hole, it possessed super activity to oxidize water into hydroxyl radicals or molecular oxygen. We hope this promising multifunctional photocatalytic material, therefore, NiO@BiOCl can be applied in advanced treatment of organic wastewater and oxygen production from photolysis water.</description><identifier>EISSN: 2073-4344</identifier><identifier>DOI: 10.3390/catal10090958</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Bands ; Catalysts ; Chemical potential ; Chemical reactions ; Crystal surfaces ; Efficiency ; Electron paramagnetic resonance ; Electron spin ; First principles ; Heterojunctions ; Heterostructures ; Hydroxyl radicals ; Light ; Mathematical analysis ; Nanoparticles ; Nickel oxides ; Noble metals ; Oxygen production ; Photocatalysis ; Photodegradation ; Photoluminescence ; Photolysis ; Spectrum analysis ; Spin resonance ; Vibration ; Wastewater treatment</subject><ispartof>Catalysts, 2020-01, Vol.10 (9), p.958</ispartof><rights>2020. This work is licensed under http://creativecommons.org/licenses/by/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2437230836/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2437230836?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,25753,27924,27925,37012,44590,75126</link.rule.ids></links><search><creatorcontrib>Yang, Jun</creatorcontrib><creatorcontrib>Zhu, Quanxi</creatorcontrib><creatorcontrib>Xie, Taiping</creatorcontrib><creatorcontrib>Wang, Jiankang</creatorcontrib><creatorcontrib>Yuan, Peng</creatorcontrib><creatorcontrib>Wang, Yajing</creatorcontrib><creatorcontrib>Liu, Chenglun</creatorcontrib><creatorcontrib>Xu, Longjun</creatorcontrib><title>Insights into Interface Charge Extraction in a Noble-Metal-Free Doped Z-Scheme [email protected] Heterojunction</title><title>Catalysts</title><description>It is of great significance to thoroughly explore the interface charge extraction and migration in heterojunction systems, which could guide us to synthesize higher-efficiency photocatalytic materials. A novel noble-metal-free doped Z-scheme NiO@BiOCl heterojunction was found in this work. The corresponding heterostructure, interface electron extraction, and electron migration were investigated via first-principles calculation. 5,5′-dimethyl-1-pyrroline-N-oxide (DMPO) spin-trapping electron spin resonance (ESR) and time-resolved photoluminescence (TRPL) tests were implemented to confirm the calculation results, which showed that electrons and holes stayed in the NiO (100) facet and BiOCl (110) facet, respectively. Owing to the large chemical potential of 2.40 V (vs ENHE) for the BiOCl valence-band hole, it possessed super activity to oxidize water into hydroxyl radicals or molecular oxygen. We hope this promising multifunctional photocatalytic material, therefore, NiO@BiOCl can be applied in advanced treatment of organic wastewater and oxygen production from photolysis water.</description><subject>Bands</subject><subject>Catalysts</subject><subject>Chemical potential</subject><subject>Chemical reactions</subject><subject>Crystal surfaces</subject><subject>Efficiency</subject><subject>Electron paramagnetic resonance</subject><subject>Electron spin</subject><subject>First principles</subject><subject>Heterojunctions</subject><subject>Heterostructures</subject><subject>Hydroxyl radicals</subject><subject>Light</subject><subject>Mathematical analysis</subject><subject>Nanoparticles</subject><subject>Nickel oxides</subject><subject>Noble metals</subject><subject>Oxygen production</subject><subject>Photocatalysis</subject><subject>Photodegradation</subject><subject>Photoluminescence</subject><subject>Photolysis</subject><subject>Spectrum analysis</subject><subject>Spin resonance</subject><subject>Vibration</subject><subject>Wastewater treatment</subject><issn>2073-4344</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNqNjb2OwjAQhC0kJNBBSb_S1QYnG46k5kdQQHNX3QkhYxaSKNhgb6R7fCzEAzDNFPPNjBCjRI0RCzUxmnWTKFWoYpp3RD9VM5QZZllPDEOoVVSRYJ5M-8JtbKguJQeoLDvYWCZ_1oZgXmp_IVj-s9eGK2cjABp27tiQ3FI8kCtPBAt3oxP8ym9T0pXgj666auDmHZNhOu1hTXHS1a19rgxE96ybQMOXf4jP1fJnvpaxcW8p8KF2rbcxOqQZzlJUOX7he9QDK1JPHw</recordid><startdate>20200101</startdate><enddate>20200101</enddate><creator>Yang, Jun</creator><creator>Zhu, Quanxi</creator><creator>Xie, Taiping</creator><creator>Wang, Jiankang</creator><creator>Yuan, Peng</creator><creator>Wang, Yajing</creator><creator>Liu, Chenglun</creator><creator>Xu, Longjun</creator><general>MDPI AG</general><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>HCIFZ</scope><scope>JG9</scope><scope>KB.</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20200101</creationdate><title>Insights into Interface Charge Extraction in a Noble-Metal-Free Doped Z-Scheme [email protected] Heterojunction</title><author>Yang, Jun ; 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A novel noble-metal-free doped Z-scheme NiO@BiOCl heterojunction was found in this work. The corresponding heterostructure, interface electron extraction, and electron migration were investigated via first-principles calculation. 5,5′-dimethyl-1-pyrroline-N-oxide (DMPO) spin-trapping electron spin resonance (ESR) and time-resolved photoluminescence (TRPL) tests were implemented to confirm the calculation results, which showed that electrons and holes stayed in the NiO (100) facet and BiOCl (110) facet, respectively. Owing to the large chemical potential of 2.40 V (vs ENHE) for the BiOCl valence-band hole, it possessed super activity to oxidize water into hydroxyl radicals or molecular oxygen. We hope this promising multifunctional photocatalytic material, therefore, NiO@BiOCl can be applied in advanced treatment of organic wastewater and oxygen production from photolysis water.</abstract><cop>Basel</cop><pub>MDPI AG</pub><doi>10.3390/catal10090958</doi><oa>free_for_read</oa></addata></record> |
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subjects | Bands Catalysts Chemical potential Chemical reactions Crystal surfaces Efficiency Electron paramagnetic resonance Electron spin First principles Heterojunctions Heterostructures Hydroxyl radicals Light Mathematical analysis Nanoparticles Nickel oxides Noble metals Oxygen production Photocatalysis Photodegradation Photoluminescence Photolysis Spectrum analysis Spin resonance Vibration Wastewater treatment |
title | Insights into Interface Charge Extraction in a Noble-Metal-Free Doped Z-Scheme [email protected] Heterojunction |
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