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A Z-scheme heterojunction ZIF67/N, P-WO3 nanocomposite for photocatalytic degradation of levofloxacin

In this work, a ZIF67/N, P-WO3 (ZNPW) Z-scheme heterojunction was constructed by N, P-codoped WO3 (NPW), and ZIF67 and developed as a highly efficient photocatalyst for Levofloxacin (LFX) removal. A series of characterization measurements including FTIR, XRD, SEM, DRS, PL, and XPS are conducted to c...

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Published in:Journal of solid state chemistry 2024-06, Vol.334, p.124660, Article 124660
Main Authors: Mu, Zhonghua, Liu, Dongni, Zhang, Wenzhi, Chai, Dongfeng, Dong, Guohua, Li, Jinlong, Zhao, Ming
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description In this work, a ZIF67/N, P-WO3 (ZNPW) Z-scheme heterojunction was constructed by N, P-codoped WO3 (NPW), and ZIF67 and developed as a highly efficient photocatalyst for Levofloxacin (LFX) removal. A series of characterization measurements including FTIR, XRD, SEM, DRS, PL, and XPS are conducted to confirm the formation of the ZNPW. After optimization on the composition of WO3, NPW and ZIF67, the optimal ZNPW shows superior photocatalytic activity, yielding a higher removal efficiency of LFX ∼91.2% in 100 min than those of pure WO3 (9.4%), NPW (47.8%) and ZIF67 (14.3 %). Additionally, ZNPW exhibits remarkable stability and reusability for up to five consecutive runs. Reactive species scavenging experiments and ESR have revealed that the degradation of LFX is primarily facilitated by the generation of holes (h+) and hydroxyl radicals (·OH). Moreover, the degradation process of LFX was identified through an integrated LC-MS analysis and density functional theory computation of the Fukui indices. This process consists of three pathways: the opening of the piperazinyl ring, separation of piperazinyl and quinoline moieties, and cleavage of the pyridine ring on the quinoline moieties. The superior photocatalytic properties can be attributed to the N, P co-doping in the WO3 structure and the simultaneous coupling with ZIF67, leading to the formation of a heterojunction with a reduced band gap, efficient charge separation and transport, and a new N 2p and P 2p energy level. In conclusion, this study provides novel insights into designing high-efficiency antibiotics degradation using WO3-based Z-scheme heterojunction photocatalysts. In this work, a ZIF67/N, P-WO3(ZNPW) Z-scheme heterojunction was constructed by N, P-codoped WO3(NPW), and ZIF67 and developed as a highly efficient photocatalyst for Levofloxacin (LFX) removal. After optimization on the composition of WO3, NPW, and ZIF67, the optimal ZNPW shows superior photocatalytic activity, yielding a higher removal efficiency of LFX ∼91.2% in 100 min than those of pure WO3 (9.4%), NPW (47.8%) and ZIF67 (14.3 %). Additionally, ZNPW also shows prominent stability and reusability for running 5 times. The superior photocatalytic properties can be attributed to the co-doping of non-metals in the WO3 structure and the simultaneous coupling with ZIF67, leading to the formation of a heterojunction with a reduced band gap, efficient charge separation and transport, and a new energy level. Reactive species scavenging experim
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A series of characterization measurements including FTIR, XRD, SEM, DRS, PL, and XPS are conducted to confirm the formation of the ZNPW. After optimization on the composition of WO3, NPW and ZIF67, the optimal ZNPW shows superior photocatalytic activity, yielding a higher removal efficiency of LFX ∼91.2% in 100 min than those of pure WO3 (9.4%), NPW (47.8%) and ZIF67 (14.3 %). Additionally, ZNPW exhibits remarkable stability and reusability for up to five consecutive runs. Reactive species scavenging experiments and ESR have revealed that the degradation of LFX is primarily facilitated by the generation of holes (h+) and hydroxyl radicals (·OH). Moreover, the degradation process of LFX was identified through an integrated LC-MS analysis and density functional theory computation of the Fukui indices. This process consists of three pathways: the opening of the piperazinyl ring, separation of piperazinyl and quinoline moieties, and cleavage of the pyridine ring on the quinoline moieties. The superior photocatalytic properties can be attributed to the N, P co-doping in the WO3 structure and the simultaneous coupling with ZIF67, leading to the formation of a heterojunction with a reduced band gap, efficient charge separation and transport, and a new N 2p and P 2p energy level. In conclusion, this study provides novel insights into designing high-efficiency antibiotics degradation using WO3-based Z-scheme heterojunction photocatalysts. In this work, a ZIF67/N, P-WO3(ZNPW) Z-scheme heterojunction was constructed by N, P-codoped WO3(NPW), and ZIF67 and developed as a highly efficient photocatalyst for Levofloxacin (LFX) removal. After optimization on the composition of WO3, NPW, and ZIF67, the optimal ZNPW shows superior photocatalytic activity, yielding a higher removal efficiency of LFX ∼91.2% in 100 min than those of pure WO3 (9.4%), NPW (47.8%) and ZIF67 (14.3 %). Additionally, ZNPW also shows prominent stability and reusability for running 5 times. The superior photocatalytic properties can be attributed to the co-doping of non-metals in the WO3 structure and the simultaneous coupling with ZIF67, leading to the formation of a heterojunction with a reduced band gap, efficient charge separation and transport, and a new energy level. Reactive species scavenging experiments indicated that the holes (h+) and hydroxyl radical (·OH) are mainly responsible for LFX degradation. Moreover, the LFX degradation process, identified based on an integrated LC-MS analysis and density functional theory computation of the Fukui indices, comprised of three pathways initiated by the opening of the piperazinyl ring, separation of piperazinyl and quinoline moieties, and cleavage of the the pyridine ring on the quinoline moieties. [Display omitted] •Z-scheme ZNPW system remains a strong photocatalytic redox capacity.•Z-scheme ZNPW system improves the separation of electron-hole pairs.•N, P-codoped introduces impurity states to promote charge transfer.•Possible photocatalytic reaction mechanism and degradation pathway were proposed.•The ZNPW showed good reusability and long-time stability.</description><identifier>ISSN: 0022-4596</identifier><identifier>EISSN: 1095-726X</identifier><identifier>DOI: 10.1016/j.jssc.2024.124660</identifier><language>eng</language><publisher>Elsevier Inc</publisher><subject>P-WO3 ; Photocatalytic ; Z-scheme heterojunction ; ZIF67</subject><ispartof>Journal of solid state chemistry, 2024-06, Vol.334, p.124660, Article 124660</ispartof><rights>2024 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c215t-615ac8c558e6a2c6323a4050b4fb97bb60fbdf0bd40c0e78f89b64a39c3c9cf13</citedby><cites>FETCH-LOGICAL-c215t-615ac8c558e6a2c6323a4050b4fb97bb60fbdf0bd40c0e78f89b64a39c3c9cf13</cites><orcidid>0000-0003-0755-798X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Mu, Zhonghua</creatorcontrib><creatorcontrib>Liu, Dongni</creatorcontrib><creatorcontrib>Zhang, Wenzhi</creatorcontrib><creatorcontrib>Chai, Dongfeng</creatorcontrib><creatorcontrib>Dong, Guohua</creatorcontrib><creatorcontrib>Li, Jinlong</creatorcontrib><creatorcontrib>Zhao, Ming</creatorcontrib><title>A Z-scheme heterojunction ZIF67/N, P-WO3 nanocomposite for photocatalytic degradation of levofloxacin</title><title>Journal of solid state chemistry</title><description>In this work, a ZIF67/N, P-WO3 (ZNPW) Z-scheme heterojunction was constructed by N, P-codoped WO3 (NPW), and ZIF67 and developed as a highly efficient photocatalyst for Levofloxacin (LFX) removal. A series of characterization measurements including FTIR, XRD, SEM, DRS, PL, and XPS are conducted to confirm the formation of the ZNPW. After optimization on the composition of WO3, NPW and ZIF67, the optimal ZNPW shows superior photocatalytic activity, yielding a higher removal efficiency of LFX ∼91.2% in 100 min than those of pure WO3 (9.4%), NPW (47.8%) and ZIF67 (14.3 %). Additionally, ZNPW exhibits remarkable stability and reusability for up to five consecutive runs. Reactive species scavenging experiments and ESR have revealed that the degradation of LFX is primarily facilitated by the generation of holes (h+) and hydroxyl radicals (·OH). Moreover, the degradation process of LFX was identified through an integrated LC-MS analysis and density functional theory computation of the Fukui indices. This process consists of three pathways: the opening of the piperazinyl ring, separation of piperazinyl and quinoline moieties, and cleavage of the pyridine ring on the quinoline moieties. The superior photocatalytic properties can be attributed to the N, P co-doping in the WO3 structure and the simultaneous coupling with ZIF67, leading to the formation of a heterojunction with a reduced band gap, efficient charge separation and transport, and a new N 2p and P 2p energy level. In conclusion, this study provides novel insights into designing high-efficiency antibiotics degradation using WO3-based Z-scheme heterojunction photocatalysts. In this work, a ZIF67/N, P-WO3(ZNPW) Z-scheme heterojunction was constructed by N, P-codoped WO3(NPW), and ZIF67 and developed as a highly efficient photocatalyst for Levofloxacin (LFX) removal. After optimization on the composition of WO3, NPW, and ZIF67, the optimal ZNPW shows superior photocatalytic activity, yielding a higher removal efficiency of LFX ∼91.2% in 100 min than those of pure WO3 (9.4%), NPW (47.8%) and ZIF67 (14.3 %). Additionally, ZNPW also shows prominent stability and reusability for running 5 times. The superior photocatalytic properties can be attributed to the co-doping of non-metals in the WO3 structure and the simultaneous coupling with ZIF67, leading to the formation of a heterojunction with a reduced band gap, efficient charge separation and transport, and a new energy level. Reactive species scavenging experiments indicated that the holes (h+) and hydroxyl radical (·OH) are mainly responsible for LFX degradation. Moreover, the LFX degradation process, identified based on an integrated LC-MS analysis and density functional theory computation of the Fukui indices, comprised of three pathways initiated by the opening of the piperazinyl ring, separation of piperazinyl and quinoline moieties, and cleavage of the the pyridine ring on the quinoline moieties. 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A series of characterization measurements including FTIR, XRD, SEM, DRS, PL, and XPS are conducted to confirm the formation of the ZNPW. After optimization on the composition of WO3, NPW and ZIF67, the optimal ZNPW shows superior photocatalytic activity, yielding a higher removal efficiency of LFX ∼91.2% in 100 min than those of pure WO3 (9.4%), NPW (47.8%) and ZIF67 (14.3 %). Additionally, ZNPW exhibits remarkable stability and reusability for up to five consecutive runs. Reactive species scavenging experiments and ESR have revealed that the degradation of LFX is primarily facilitated by the generation of holes (h+) and hydroxyl radicals (·OH). Moreover, the degradation process of LFX was identified through an integrated LC-MS analysis and density functional theory computation of the Fukui indices. This process consists of three pathways: the opening of the piperazinyl ring, separation of piperazinyl and quinoline moieties, and cleavage of the pyridine ring on the quinoline moieties. The superior photocatalytic properties can be attributed to the N, P co-doping in the WO3 structure and the simultaneous coupling with ZIF67, leading to the formation of a heterojunction with a reduced band gap, efficient charge separation and transport, and a new N 2p and P 2p energy level. In conclusion, this study provides novel insights into designing high-efficiency antibiotics degradation using WO3-based Z-scheme heterojunction photocatalysts. In this work, a ZIF67/N, P-WO3(ZNPW) Z-scheme heterojunction was constructed by N, P-codoped WO3(NPW), and ZIF67 and developed as a highly efficient photocatalyst for Levofloxacin (LFX) removal. After optimization on the composition of WO3, NPW, and ZIF67, the optimal ZNPW shows superior photocatalytic activity, yielding a higher removal efficiency of LFX ∼91.2% in 100 min than those of pure WO3 (9.4%), NPW (47.8%) and ZIF67 (14.3 %). Additionally, ZNPW also shows prominent stability and reusability for running 5 times. The superior photocatalytic properties can be attributed to the co-doping of non-metals in the WO3 structure and the simultaneous coupling with ZIF67, leading to the formation of a heterojunction with a reduced band gap, efficient charge separation and transport, and a new energy level. Reactive species scavenging experiments indicated that the holes (h+) and hydroxyl radical (·OH) are mainly responsible for LFX degradation. Moreover, the LFX degradation process, identified based on an integrated LC-MS analysis and density functional theory computation of the Fukui indices, comprised of three pathways initiated by the opening of the piperazinyl ring, separation of piperazinyl and quinoline moieties, and cleavage of the the pyridine ring on the quinoline moieties. [Display omitted] •Z-scheme ZNPW system remains a strong photocatalytic redox capacity.•Z-scheme ZNPW system improves the separation of electron-hole pairs.•N, P-codoped introduces impurity states to promote charge transfer.•Possible photocatalytic reaction mechanism and degradation pathway were proposed.•The ZNPW showed good reusability and long-time stability.</abstract><pub>Elsevier Inc</pub><doi>10.1016/j.jssc.2024.124660</doi><orcidid>https://orcid.org/0000-0003-0755-798X</orcidid></addata></record>
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Photocatalytic
Z-scheme heterojunction
ZIF67
title A Z-scheme heterojunction ZIF67/N, P-WO3 nanocomposite for photocatalytic degradation of levofloxacin
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