CdS Nanoparticles Supported on a Dual Metal–Organic Framework as a Catalyst for the Photodegradation of Tetracycline

The photocatalytic activity of individual metal–organic frameworks (MOFs) such as UiO-66-NH2 and MIL-101­(Fe) is less satisfactory due to the disappointing separation rate of electron–hole pairs and weak solar energy utilization efficiency. In this context, we develop hierarchical dual Z-scheme hete...

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Veröffentlicht in:ACS applied nano materials 2024-02, Vol.7 (3), p.3154-3167
Hauptverfasser: Jin, Yuning, Mi, Xichen, Qian, Jianglu, Ma, Na, Dai, Wei
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creator Jin, Yuning
Mi, Xichen
Qian, Jianglu
Ma, Na
Dai, Wei
description The photocatalytic activity of individual metal–organic frameworks (MOFs) such as UiO-66-NH2 and MIL-101­(Fe) is less satisfactory due to the disappointing separation rate of electron–hole pairs and weak solar energy utilization efficiency. In this context, we develop hierarchical dual Z-scheme heterostructured photocatalysts prepared via an in situ hydrothermal synthesis method anchoring cadmium sulfide (CdS) nanoparticles onto the (UiO-66-NH2)-(MIL-101­(Fe)) (UM) dual metal–organic frameworks. Attributed to the synergistic effects of CdS, UiO-66-NH2, and MIL-101­(Fe), the (UiO-66-NH2)-(MIL-101)­(Fe)-CdS (UM-CdS) exhibits outstanding degradation activities toward TC degradability. Typically, 10 mg of UM-CdS achieved an 87% degradation rate of TC within 140 min, which is 8.7, 2.4, and 1.4 times than those of UiO-66-NH2, MIL-101­(Fe), and CdS, which achieved higher photocatalytic degradation rate with a less dosage of catalysts compared with previous reports. The outstanding photocatalytic activity of UM-CdS is primarily attributed to its hierarchical structure, which provides numerous active sites. Additionally, the special heterostructure not only exhibits a dual Z-scheme migration mechanism for charge carriers, which facilitates the efficient separation and migration of photoinduced electrons and holes, but also promotes the redox capability of UM-CdS. Furthermore, the trapping tests demonstrated that •O2 –, •OH, and h+ were the main active species during the photocatalytic process. The degradation products or intermediates were also studied in-depth through the liquid chromatography–mass spectrometry (LC-MS) technique. Besides, the UM-CdS possesses excellent stability, retaining more than 90% initial photocatalytic activity after the fifth cycle. This work provides a double MOF-supported CdS strategy to prepare recyclable dual Z-scheme heterojunction photocatalysts for the degradation of refractory antibiotics (e.g., TC) in sewage.
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In this context, we develop hierarchical dual Z-scheme heterostructured photocatalysts prepared via an in situ hydrothermal synthesis method anchoring cadmium sulfide (CdS) nanoparticles onto the (UiO-66-NH2)-(MIL-101­(Fe)) (UM) dual metal–organic frameworks. Attributed to the synergistic effects of CdS, UiO-66-NH2, and MIL-101­(Fe), the (UiO-66-NH2)-(MIL-101)­(Fe)-CdS (UM-CdS) exhibits outstanding degradation activities toward TC degradability. Typically, 10 mg of UM-CdS achieved an 87% degradation rate of TC within 140 min, which is 8.7, 2.4, and 1.4 times than those of UiO-66-NH2, MIL-101­(Fe), and CdS, which achieved higher photocatalytic degradation rate with a less dosage of catalysts compared with previous reports. The outstanding photocatalytic activity of UM-CdS is primarily attributed to its hierarchical structure, which provides numerous active sites. Additionally, the special heterostructure not only exhibits a dual Z-scheme migration mechanism for charge carriers, which facilitates the efficient separation and migration of photoinduced electrons and holes, but also promotes the redox capability of UM-CdS. Furthermore, the trapping tests demonstrated that •O2 –, •OH, and h+ were the main active species during the photocatalytic process. The degradation products or intermediates were also studied in-depth through the liquid chromatography–mass spectrometry (LC-MS) technique. Besides, the UM-CdS possesses excellent stability, retaining more than 90% initial photocatalytic activity after the fifth cycle. 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Nano Mater</addtitle><description>The photocatalytic activity of individual metal–organic frameworks (MOFs) such as UiO-66-NH2 and MIL-101­(Fe) is less satisfactory due to the disappointing separation rate of electron–hole pairs and weak solar energy utilization efficiency. In this context, we develop hierarchical dual Z-scheme heterostructured photocatalysts prepared via an in situ hydrothermal synthesis method anchoring cadmium sulfide (CdS) nanoparticles onto the (UiO-66-NH2)-(MIL-101­(Fe)) (UM) dual metal–organic frameworks. Attributed to the synergistic effects of CdS, UiO-66-NH2, and MIL-101­(Fe), the (UiO-66-NH2)-(MIL-101)­(Fe)-CdS (UM-CdS) exhibits outstanding degradation activities toward TC degradability. Typically, 10 mg of UM-CdS achieved an 87% degradation rate of TC within 140 min, which is 8.7, 2.4, and 1.4 times than those of UiO-66-NH2, MIL-101­(Fe), and CdS, which achieved higher photocatalytic degradation rate with a less dosage of catalysts compared with previous reports. The outstanding photocatalytic activity of UM-CdS is primarily attributed to its hierarchical structure, which provides numerous active sites. Additionally, the special heterostructure not only exhibits a dual Z-scheme migration mechanism for charge carriers, which facilitates the efficient separation and migration of photoinduced electrons and holes, but also promotes the redox capability of UM-CdS. Furthermore, the trapping tests demonstrated that •O2 –, •OH, and h+ were the main active species during the photocatalytic process. The degradation products or intermediates were also studied in-depth through the liquid chromatography–mass spectrometry (LC-MS) technique. Besides, the UM-CdS possesses excellent stability, retaining more than 90% initial photocatalytic activity after the fifth cycle. 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Nano Mater</addtitle><date>2024-02-09</date><risdate>2024</risdate><volume>7</volume><issue>3</issue><spage>3154</spage><epage>3167</epage><pages>3154-3167</pages><issn>2574-0970</issn><eissn>2574-0970</eissn><abstract>The photocatalytic activity of individual metal–organic frameworks (MOFs) such as UiO-66-NH2 and MIL-101­(Fe) is less satisfactory due to the disappointing separation rate of electron–hole pairs and weak solar energy utilization efficiency. In this context, we develop hierarchical dual Z-scheme heterostructured photocatalysts prepared via an in situ hydrothermal synthesis method anchoring cadmium sulfide (CdS) nanoparticles onto the (UiO-66-NH2)-(MIL-101­(Fe)) (UM) dual metal–organic frameworks. Attributed to the synergistic effects of CdS, UiO-66-NH2, and MIL-101­(Fe), the (UiO-66-NH2)-(MIL-101)­(Fe)-CdS (UM-CdS) exhibits outstanding degradation activities toward TC degradability. Typically, 10 mg of UM-CdS achieved an 87% degradation rate of TC within 140 min, which is 8.7, 2.4, and 1.4 times than those of UiO-66-NH2, MIL-101­(Fe), and CdS, which achieved higher photocatalytic degradation rate with a less dosage of catalysts compared with previous reports. The outstanding photocatalytic activity of UM-CdS is primarily attributed to its hierarchical structure, which provides numerous active sites. Additionally, the special heterostructure not only exhibits a dual Z-scheme migration mechanism for charge carriers, which facilitates the efficient separation and migration of photoinduced electrons and holes, but also promotes the redox capability of UM-CdS. Furthermore, the trapping tests demonstrated that •O2 –, •OH, and h+ were the main active species during the photocatalytic process. The degradation products or intermediates were also studied in-depth through the liquid chromatography–mass spectrometry (LC-MS) technique. Besides, the UM-CdS possesses excellent stability, retaining more than 90% initial photocatalytic activity after the fifth cycle. This work provides a double MOF-supported CdS strategy to prepare recyclable dual Z-scheme heterojunction photocatalysts for the degradation of refractory antibiotics (e.g., TC) in sewage.</abstract><pub>American Chemical Society</pub><doi>10.1021/acsanm.3c05511</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0001-9377-1151</orcidid></addata></record>
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