Construction of Amorphous CoS/CdS Nanoparticles Heterojunctions for Visible–Light–Driven Photocatalytic H2 Evolution

Due to the poor photocatalytic hydrogen evolution ability of pure CdS, we need to develop a photocatalytic hydrogen evolution catalyst with high activity and no precious metal doping. Therefore, in this article, we used a simple hydrothermal synthesis of CdS nanoparticles, using water as a carrier,...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Catalysis letters 2021-08, Vol.151 (8), p.2408-2419
Hauptverfasser: Li, Xuanhao, Xu, Jing, Li, Lingjiao, Zhao, Sheng, Mao, Min, Liu, Zeying, Li, Yanru
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 2419
container_issue 8
container_start_page 2408
container_title Catalysis letters
container_volume 151
creator Li, Xuanhao
Xu, Jing
Li, Lingjiao
Zhao, Sheng
Mao, Min
Liu, Zeying
Li, Yanru
description Due to the poor photocatalytic hydrogen evolution ability of pure CdS, we need to develop a photocatalytic hydrogen evolution catalyst with high activity and no precious metal doping. Therefore, in this article, we used a simple hydrothermal synthesis of CdS nanoparticles, using water as a carrier, loading a small amount of amorphous CoS, by changing the loading ratio of amorphous CoS, synthesized TYPE–II type heterojunction composite catalyst CCS. The successful synthesis of the composite catalyst CCS was verified by XRD, SEM and other characterization methods. UV–vis, PL and other characterization showed that the supported amorphous CoS could significantly improve the photocatalytic activity of CdS, and the photochemical detection also showed that the performance of composite catalyst CCS was better than that of pure CdS. Using Na 2 S and Na 2 SO 3 mixed solution as electron sacrificial agent, the hydrogen production performance of CCS composite catalyst was determined through hydrogen evolution experiment and cyclic stability experiment. It was found that the sacrificial agent had a great promotion effect on the hydrogen production performance of photocatalyst. It was found that the hydrogen production rate of the composite catalyst could reach 2.01 mmol·g −1 ·h −1 , which was 6.3 times of the pure CdS. This study offers a novel approach for the design of amorphous–based nanostructures as efficient hydrogen evolution cocatalysts. Graphic Abstract First, CdS are excited by light, consuming S 2− and SO 3 2− ions in the sacrificial agent, generating a large number of electrons and holes. Due to the energy difference between the conducting band (CB) of CdS and amorphous CoS, the electrons are transferred from the surface of CdS to the conducting band (CB) of amorphous CoS, while the electrons obtained from water and H + in the sacrificial agent are reduced to H 2 . The amorphous CoS is used as the transfer medium of electron acceptor, and the synergistic effect between heterojunctions is used to improve the charge separation efficiency and electron transfer rate. Therefore, the photocatalytic hydrogen production effect of the composite catalyst CCS–7 has been greatly improved.
doi_str_mv 10.1007/s10562-020-03468-6
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2547179588</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2547179588</sourcerecordid><originalsourceid>FETCH-LOGICAL-c2346-addba7621c17eedf34708db8dd54962bb57b73bcc2d7322dff869b2356af65b13</originalsourceid><addsrcrecordid>eNp9kMtOwzAQRSMEEqXwA6wssTb1I7GTZRUeRaoAqYC6s-zYaVOlcbGTiu74B_6QL8FtkNixmlncc0dzougSo2uMEB95jBJGICIIIhqzFLKjaIATTmDKs_lx2BHGkHIyP43OvF8hhDKOs0H0kdvGt64r2so2wJZgvLZus7SdB7mdjXI9A4-ysRvp2qqojQcT0xpnV11zIDworQNvla9Ubb4_v6bVYtmGeeOqrWnA89K2tpCtrHcBBxMCbre27vbkeXRSytqbi985jF7vbl_yCZw-3T_k4yksSHgESq2V5IzgAnNjdEljjlKtUq2TOGNEqYQrTlVREM0pIbosU5YpQhMmS5YoTIfRVd-7cfa9M74VK9u5JpwUJIk55lmSpiFF-lThrPfOlGLjqrV0O4GR2BsWvWERDIuDYcECRHvIh3CzMO6v-h_qB9tugvY</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2547179588</pqid></control><display><type>article</type><title>Construction of Amorphous CoS/CdS Nanoparticles Heterojunctions for Visible–Light–Driven Photocatalytic H2 Evolution</title><source>SpringerLink Journals - AutoHoldings</source><creator>Li, Xuanhao ; Xu, Jing ; Li, Lingjiao ; Zhao, Sheng ; Mao, Min ; Liu, Zeying ; Li, Yanru</creator><creatorcontrib>Li, Xuanhao ; Xu, Jing ; Li, Lingjiao ; Zhao, Sheng ; Mao, Min ; Liu, Zeying ; Li, Yanru</creatorcontrib><description>Due to the poor photocatalytic hydrogen evolution ability of pure CdS, we need to develop a photocatalytic hydrogen evolution catalyst with high activity and no precious metal doping. Therefore, in this article, we used a simple hydrothermal synthesis of CdS nanoparticles, using water as a carrier, loading a small amount of amorphous CoS, by changing the loading ratio of amorphous CoS, synthesized TYPE–II type heterojunction composite catalyst CCS. The successful synthesis of the composite catalyst CCS was verified by XRD, SEM and other characterization methods. UV–vis, PL and other characterization showed that the supported amorphous CoS could significantly improve the photocatalytic activity of CdS, and the photochemical detection also showed that the performance of composite catalyst CCS was better than that of pure CdS. Using Na 2 S and Na 2 SO 3 mixed solution as electron sacrificial agent, the hydrogen production performance of CCS composite catalyst was determined through hydrogen evolution experiment and cyclic stability experiment. It was found that the sacrificial agent had a great promotion effect on the hydrogen production performance of photocatalyst. It was found that the hydrogen production rate of the composite catalyst could reach 2.01 mmol·g −1 ·h −1 , which was 6.3 times of the pure CdS. This study offers a novel approach for the design of amorphous–based nanostructures as efficient hydrogen evolution cocatalysts. Graphic Abstract First, CdS are excited by light, consuming S 2− and SO 3 2− ions in the sacrificial agent, generating a large number of electrons and holes. Due to the energy difference between the conducting band (CB) of CdS and amorphous CoS, the electrons are transferred from the surface of CdS to the conducting band (CB) of amorphous CoS, while the electrons obtained from water and H + in the sacrificial agent are reduced to H 2 . The amorphous CoS is used as the transfer medium of electron acceptor, and the synergistic effect between heterojunctions is used to improve the charge separation efficiency and electron transfer rate. Therefore, the photocatalytic hydrogen production effect of the composite catalyst CCS–7 has been greatly improved.</description><identifier>ISSN: 1011-372X</identifier><identifier>EISSN: 1572-879X</identifier><identifier>DOI: 10.1007/s10562-020-03468-6</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Cadmium sulfide ; Catalysis ; Catalysts ; Catalytic activity ; Charge efficiency ; Chemical synthesis ; Chemistry ; Chemistry and Materials Science ; Electron transfer ; Electrons ; Heterojunctions ; Hydrogen ; Hydrogen evolution ; Hydrogen production ; Industrial Chemistry/Chemical Engineering ; Nanoparticles ; Organometallic Chemistry ; Photocatalysis ; Physical Chemistry ; Sodium sulfide ; Sodium sulfite ; Synergistic effect</subject><ispartof>Catalysis letters, 2021-08, Vol.151 (8), p.2408-2419</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature 2021</rights><rights>Springer Science+Business Media, LLC, part of Springer Nature 2021.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2346-addba7621c17eedf34708db8dd54962bb57b73bcc2d7322dff869b2356af65b13</citedby><cites>FETCH-LOGICAL-c2346-addba7621c17eedf34708db8dd54962bb57b73bcc2d7322dff869b2356af65b13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10562-020-03468-6$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10562-020-03468-6$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27923,27924,41487,42556,51318</link.rule.ids></links><search><creatorcontrib>Li, Xuanhao</creatorcontrib><creatorcontrib>Xu, Jing</creatorcontrib><creatorcontrib>Li, Lingjiao</creatorcontrib><creatorcontrib>Zhao, Sheng</creatorcontrib><creatorcontrib>Mao, Min</creatorcontrib><creatorcontrib>Liu, Zeying</creatorcontrib><creatorcontrib>Li, Yanru</creatorcontrib><title>Construction of Amorphous CoS/CdS Nanoparticles Heterojunctions for Visible–Light–Driven Photocatalytic H2 Evolution</title><title>Catalysis letters</title><addtitle>Catal Lett</addtitle><description>Due to the poor photocatalytic hydrogen evolution ability of pure CdS, we need to develop a photocatalytic hydrogen evolution catalyst with high activity and no precious metal doping. Therefore, in this article, we used a simple hydrothermal synthesis of CdS nanoparticles, using water as a carrier, loading a small amount of amorphous CoS, by changing the loading ratio of amorphous CoS, synthesized TYPE–II type heterojunction composite catalyst CCS. The successful synthesis of the composite catalyst CCS was verified by XRD, SEM and other characterization methods. UV–vis, PL and other characterization showed that the supported amorphous CoS could significantly improve the photocatalytic activity of CdS, and the photochemical detection also showed that the performance of composite catalyst CCS was better than that of pure CdS. Using Na 2 S and Na 2 SO 3 mixed solution as electron sacrificial agent, the hydrogen production performance of CCS composite catalyst was determined through hydrogen evolution experiment and cyclic stability experiment. It was found that the sacrificial agent had a great promotion effect on the hydrogen production performance of photocatalyst. It was found that the hydrogen production rate of the composite catalyst could reach 2.01 mmol·g −1 ·h −1 , which was 6.3 times of the pure CdS. This study offers a novel approach for the design of amorphous–based nanostructures as efficient hydrogen evolution cocatalysts. Graphic Abstract First, CdS are excited by light, consuming S 2− and SO 3 2− ions in the sacrificial agent, generating a large number of electrons and holes. Due to the energy difference between the conducting band (CB) of CdS and amorphous CoS, the electrons are transferred from the surface of CdS to the conducting band (CB) of amorphous CoS, while the electrons obtained from water and H + in the sacrificial agent are reduced to H 2 . The amorphous CoS is used as the transfer medium of electron acceptor, and the synergistic effect between heterojunctions is used to improve the charge separation efficiency and electron transfer rate. Therefore, the photocatalytic hydrogen production effect of the composite catalyst CCS–7 has been greatly improved.</description><subject>Cadmium sulfide</subject><subject>Catalysis</subject><subject>Catalysts</subject><subject>Catalytic activity</subject><subject>Charge efficiency</subject><subject>Chemical synthesis</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Electron transfer</subject><subject>Electrons</subject><subject>Heterojunctions</subject><subject>Hydrogen</subject><subject>Hydrogen evolution</subject><subject>Hydrogen production</subject><subject>Industrial Chemistry/Chemical Engineering</subject><subject>Nanoparticles</subject><subject>Organometallic Chemistry</subject><subject>Photocatalysis</subject><subject>Physical Chemistry</subject><subject>Sodium sulfide</subject><subject>Sodium sulfite</subject><subject>Synergistic effect</subject><issn>1011-372X</issn><issn>1572-879X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNp9kMtOwzAQRSMEEqXwA6wssTb1I7GTZRUeRaoAqYC6s-zYaVOlcbGTiu74B_6QL8FtkNixmlncc0dzougSo2uMEB95jBJGICIIIhqzFLKjaIATTmDKs_lx2BHGkHIyP43OvF8hhDKOs0H0kdvGt64r2so2wJZgvLZus7SdB7mdjXI9A4-ysRvp2qqojQcT0xpnV11zIDworQNvla9Ubb4_v6bVYtmGeeOqrWnA89K2tpCtrHcBBxMCbre27vbkeXRSytqbi985jF7vbl_yCZw-3T_k4yksSHgESq2V5IzgAnNjdEljjlKtUq2TOGNEqYQrTlVREM0pIbosU5YpQhMmS5YoTIfRVd-7cfa9M74VK9u5JpwUJIk55lmSpiFF-lThrPfOlGLjqrV0O4GR2BsWvWERDIuDYcECRHvIh3CzMO6v-h_qB9tugvY</recordid><startdate>20210801</startdate><enddate>20210801</enddate><creator>Li, Xuanhao</creator><creator>Xu, Jing</creator><creator>Li, Lingjiao</creator><creator>Zhao, Sheng</creator><creator>Mao, Min</creator><creator>Liu, Zeying</creator><creator>Li, Yanru</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>HCIFZ</scope><scope>KB.</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20210801</creationdate><title>Construction of Amorphous CoS/CdS Nanoparticles Heterojunctions for Visible–Light–Driven Photocatalytic H2 Evolution</title><author>Li, Xuanhao ; Xu, Jing ; Li, Lingjiao ; Zhao, Sheng ; Mao, Min ; Liu, Zeying ; Li, Yanru</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2346-addba7621c17eedf34708db8dd54962bb57b73bcc2d7322dff869b2356af65b13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Cadmium sulfide</topic><topic>Catalysis</topic><topic>Catalysts</topic><topic>Catalytic activity</topic><topic>Charge efficiency</topic><topic>Chemical synthesis</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Electron transfer</topic><topic>Electrons</topic><topic>Heterojunctions</topic><topic>Hydrogen</topic><topic>Hydrogen evolution</topic><topic>Hydrogen production</topic><topic>Industrial Chemistry/Chemical Engineering</topic><topic>Nanoparticles</topic><topic>Organometallic Chemistry</topic><topic>Photocatalysis</topic><topic>Physical Chemistry</topic><topic>Sodium sulfide</topic><topic>Sodium sulfite</topic><topic>Synergistic effect</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Xuanhao</creatorcontrib><creatorcontrib>Xu, Jing</creatorcontrib><creatorcontrib>Li, Lingjiao</creatorcontrib><creatorcontrib>Zhao, Sheng</creatorcontrib><creatorcontrib>Mao, Min</creatorcontrib><creatorcontrib>Liu, Zeying</creatorcontrib><creatorcontrib>Li, Yanru</creatorcontrib><collection>CrossRef</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>Materials Science &amp; Engineering Collection</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>SciTech Premium Collection</collection><collection>Materials Science Database</collection><collection>Materials Science Collection</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>Catalysis letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Xuanhao</au><au>Xu, Jing</au><au>Li, Lingjiao</au><au>Zhao, Sheng</au><au>Mao, Min</au><au>Liu, Zeying</au><au>Li, Yanru</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Construction of Amorphous CoS/CdS Nanoparticles Heterojunctions for Visible–Light–Driven Photocatalytic H2 Evolution</atitle><jtitle>Catalysis letters</jtitle><stitle>Catal Lett</stitle><date>2021-08-01</date><risdate>2021</risdate><volume>151</volume><issue>8</issue><spage>2408</spage><epage>2419</epage><pages>2408-2419</pages><issn>1011-372X</issn><eissn>1572-879X</eissn><abstract>Due to the poor photocatalytic hydrogen evolution ability of pure CdS, we need to develop a photocatalytic hydrogen evolution catalyst with high activity and no precious metal doping. Therefore, in this article, we used a simple hydrothermal synthesis of CdS nanoparticles, using water as a carrier, loading a small amount of amorphous CoS, by changing the loading ratio of amorphous CoS, synthesized TYPE–II type heterojunction composite catalyst CCS. The successful synthesis of the composite catalyst CCS was verified by XRD, SEM and other characterization methods. UV–vis, PL and other characterization showed that the supported amorphous CoS could significantly improve the photocatalytic activity of CdS, and the photochemical detection also showed that the performance of composite catalyst CCS was better than that of pure CdS. Using Na 2 S and Na 2 SO 3 mixed solution as electron sacrificial agent, the hydrogen production performance of CCS composite catalyst was determined through hydrogen evolution experiment and cyclic stability experiment. It was found that the sacrificial agent had a great promotion effect on the hydrogen production performance of photocatalyst. It was found that the hydrogen production rate of the composite catalyst could reach 2.01 mmol·g −1 ·h −1 , which was 6.3 times of the pure CdS. This study offers a novel approach for the design of amorphous–based nanostructures as efficient hydrogen evolution cocatalysts. Graphic Abstract First, CdS are excited by light, consuming S 2− and SO 3 2− ions in the sacrificial agent, generating a large number of electrons and holes. Due to the energy difference between the conducting band (CB) of CdS and amorphous CoS, the electrons are transferred from the surface of CdS to the conducting band (CB) of amorphous CoS, while the electrons obtained from water and H + in the sacrificial agent are reduced to H 2 . The amorphous CoS is used as the transfer medium of electron acceptor, and the synergistic effect between heterojunctions is used to improve the charge separation efficiency and electron transfer rate. Therefore, the photocatalytic hydrogen production effect of the composite catalyst CCS–7 has been greatly improved.</abstract><cop>New York</cop><pub>Springer US</pub><doi>10.1007/s10562-020-03468-6</doi><tpages>12</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1011-372X
ispartof Catalysis letters, 2021-08, Vol.151 (8), p.2408-2419
issn 1011-372X
1572-879X
language eng
recordid cdi_proquest_journals_2547179588
source SpringerLink Journals - AutoHoldings
subjects Cadmium sulfide
Catalysis
Catalysts
Catalytic activity
Charge efficiency
Chemical synthesis
Chemistry
Chemistry and Materials Science
Electron transfer
Electrons
Heterojunctions
Hydrogen
Hydrogen evolution
Hydrogen production
Industrial Chemistry/Chemical Engineering
Nanoparticles
Organometallic Chemistry
Photocatalysis
Physical Chemistry
Sodium sulfide
Sodium sulfite
Synergistic effect
title Construction of Amorphous CoS/CdS Nanoparticles Heterojunctions for Visible–Light–Driven Photocatalytic H2 Evolution
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-11T19%3A09%3A20IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Construction%20of%20Amorphous%20CoS/CdS%20Nanoparticles%20Heterojunctions%20for%20Visible%E2%80%93Light%E2%80%93Driven%20Photocatalytic%20H2%20Evolution&rft.jtitle=Catalysis%20letters&rft.au=Li,%20Xuanhao&rft.date=2021-08-01&rft.volume=151&rft.issue=8&rft.spage=2408&rft.epage=2419&rft.pages=2408-2419&rft.issn=1011-372X&rft.eissn=1572-879X&rft_id=info:doi/10.1007/s10562-020-03468-6&rft_dat=%3Cproquest_cross%3E2547179588%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2547179588&rft_id=info:pmid/&rfr_iscdi=true