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Engineering Zn1-xCdxS/CdS Heterostructures with Enhanced Photocatalytic Activity
Various porous Zn1-xCdxS/CdS heteorostructures were achieved via in situ synthesis method with organic amines as the templates. Because of the larger radius of Cd(2+) than that of Zn(2+), CdS quantum dots are formed and distributed uniformly in the network of Zn1-xCdxS. The Zn1-xCdxS/CdS heterostruc...
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Published in: | ACS applied materials & interfaces 2016-06, Vol.8 (23), p.14535-14541 |
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container_start_page | 14535 |
container_title | ACS applied materials & interfaces |
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creator | Li, Kui Chen, Rong Li, Shun-Li Xie, Shuai-Lei Dong, Long-Zhang Kang, Zhen-Hui Bao, Jian-Chun Lan, Ya-Qian |
description | Various porous Zn1-xCdxS/CdS heteorostructures were achieved via in situ synthesis method with organic amines as the templates. Because of the larger radius of Cd(2+) than that of Zn(2+), CdS quantum dots are formed and distributed uniformly in the network of Zn1-xCdxS. The Zn1-xCdxS/CdS heterostructure with small Cd content (10 at%) derived from ethylenediamine shows very high H2-evolution rate of 667.5 μmol/h per 5 mg photocatalyst under visible light (λ ≥ 420 nm) with an apparent quantum efficiency of 50.1% per 5 mg at 420 nm. Moreover, this Zn1-xCdxS/CdS heterostructure photocatalyst also shows an excellent photocatalytic stability over 100 h. |
doi_str_mv | 10.1021/acsami.6b02765 |
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Because of the larger radius of Cd(2+) than that of Zn(2+), CdS quantum dots are formed and distributed uniformly in the network of Zn1-xCdxS. The Zn1-xCdxS/CdS heterostructure with small Cd content (10 at%) derived from ethylenediamine shows very high H2-evolution rate of 667.5 μmol/h per 5 mg photocatalyst under visible light (λ ≥ 420 nm) with an apparent quantum efficiency of 50.1% per 5 mg at 420 nm. Moreover, this Zn1-xCdxS/CdS heterostructure photocatalyst also shows an excellent photocatalytic stability over 100 h.</description><identifier>EISSN: 1944-8252</identifier><identifier>DOI: 10.1021/acsami.6b02765</identifier><identifier>PMID: 27172231</identifier><language>eng</language><publisher>United States</publisher><ispartof>ACS applied materials & interfaces, 2016-06, Vol.8 (23), p.14535-14541</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,786,790,27957,27958</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27172231$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Kui</creatorcontrib><creatorcontrib>Chen, Rong</creatorcontrib><creatorcontrib>Li, Shun-Li</creatorcontrib><creatorcontrib>Xie, Shuai-Lei</creatorcontrib><creatorcontrib>Dong, Long-Zhang</creatorcontrib><creatorcontrib>Kang, Zhen-Hui</creatorcontrib><creatorcontrib>Bao, Jian-Chun</creatorcontrib><creatorcontrib>Lan, Ya-Qian</creatorcontrib><title>Engineering Zn1-xCdxS/CdS Heterostructures with Enhanced Photocatalytic Activity</title><title>ACS applied materials & interfaces</title><addtitle>ACS Appl Mater Interfaces</addtitle><description>Various porous Zn1-xCdxS/CdS heteorostructures were achieved via in situ synthesis method with organic amines as the templates. Because of the larger radius of Cd(2+) than that of Zn(2+), CdS quantum dots are formed and distributed uniformly in the network of Zn1-xCdxS. The Zn1-xCdxS/CdS heterostructure with small Cd content (10 at%) derived from ethylenediamine shows very high H2-evolution rate of 667.5 μmol/h per 5 mg photocatalyst under visible light (λ ≥ 420 nm) with an apparent quantum efficiency of 50.1% per 5 mg at 420 nm. 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title | Engineering Zn1-xCdxS/CdS Heterostructures with Enhanced Photocatalytic Activity |
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