Comparative activity of aqueous dispersions of CdS nanocrystals stabilized by cationic and anionic polyelectrolytes in photocatalytic hydrogen production from water
The results of a study on the photocatalytic activity of aqueous dispersions of Ni-doped CdS nanocrystals (NCs) covered with an amphiphilic polyelectrolyte (PE) shell, i.e. , a polycation (NC-PC) or polyanion (NC-PA), are presented for the first time. The H 2 evolution rate measured under identical...
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Veröffentlicht in: | Russian chemical bulletin 2018-10, Vol.67 (10), p.1803-1806 |
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creator | Kabachii, Yu. A. Kochev, S. Yu Alenichev, M. K. Antonova, O. Yu Sadagov, A. Yu Valetskii, P. M. Nadtochenko, V. A. |
description | The results of a study on the photocatalytic activity of aqueous dispersions of Ni-doped CdS nanocrystals (NCs) covered with an amphiphilic polyelectrolyte (PE) shell,
i.e.
, a polycation (NC-PC) or polyanion (NC-PA), are presented for the first time. The H
2
evolution rate measured under identical conditions served as a measure of activity. The NC-PC and NC-PA samples were characterized by similar PE content (~40%) and monomodal size distribution. According to our calculations based on the NC dimensions and lattice parameters, about one macromolecule of the PE is required to stabilize one NC. The average hydrodynamic diameter of the NC-PC was found to be 1.5 times larger than that of the NC-PA due to the difference between their chemical structures and different abilities of ionogenic groups to dissociate. The photocatal ytic activity of the PE-stabilized CdS nanocrystals was significantly influenced by the type of the PE, while the H
2
evolution rate depended on the reducing medium used during the process. When the medium contained Na
2
S or when the PE-stabilized NCs were pretreated with Na
2
S, the effect of the shell type was more pronounced and the activity of NC-PA was 2 to 14 times higher than that of NC-PC. |
doi_str_mv | 10.1007/s11172-018-2292-3 |
format | Article |
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i.e.
, a polycation (NC-PC) or polyanion (NC-PA), are presented for the first time. The H
2
evolution rate measured under identical conditions served as a measure of activity. The NC-PC and NC-PA samples were characterized by similar PE content (~40%) and monomodal size distribution. According to our calculations based on the NC dimensions and lattice parameters, about one macromolecule of the PE is required to stabilize one NC. The average hydrodynamic diameter of the NC-PC was found to be 1.5 times larger than that of the NC-PA due to the difference between their chemical structures and different abilities of ionogenic groups to dissociate. The photocatal ytic activity of the PE-stabilized CdS nanocrystals was significantly influenced by the type of the PE, while the H
2
evolution rate depended on the reducing medium used during the process. When the medium contained Na
2
S or when the PE-stabilized NCs were pretreated with Na
2
S, the effect of the shell type was more pronounced and the activity of NC-PA was 2 to 14 times higher than that of NC-PC.</description><identifier>ISSN: 1066-5285</identifier><identifier>EISSN: 1573-9171</identifier><identifier>DOI: 10.1007/s11172-018-2292-3</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Catalytic activity ; Chemistry ; Chemistry and Materials Science ; Chemistry/Food Science ; Dispersions ; Hydrogen evolution ; Hydrogen production ; Inorganic Chemistry ; Lattice parameters ; Nanocrystals ; Nickel ; Organic Chemistry ; Photocatalysis ; Polyelectrolytes ; Size distribution ; Sodium sulfide</subject><ispartof>Russian chemical bulletin, 2018-10, Vol.67 (10), p.1803-1806</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature 2018</rights><rights>Copyright Springer Science & Business Media 2018</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c316t-8f79bf40dc3f76858eee9ddf04e58e763e1f3a952c1cef151d3b6f149e37caa13</citedby><cites>FETCH-LOGICAL-c316t-8f79bf40dc3f76858eee9ddf04e58e763e1f3a952c1cef151d3b6f149e37caa13</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/s11172-018-2292-3$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11172-018-2292-3$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids></links><search><creatorcontrib>Kabachii, Yu. A.</creatorcontrib><creatorcontrib>Kochev, S. Yu</creatorcontrib><creatorcontrib>Alenichev, M. K.</creatorcontrib><creatorcontrib>Antonova, O. Yu</creatorcontrib><creatorcontrib>Sadagov, A. Yu</creatorcontrib><creatorcontrib>Valetskii, P. M.</creatorcontrib><creatorcontrib>Nadtochenko, V. A.</creatorcontrib><title>Comparative activity of aqueous dispersions of CdS nanocrystals stabilized by cationic and anionic polyelectrolytes in photocatalytic hydrogen production from water</title><title>Russian chemical bulletin</title><addtitle>Russ Chem Bull</addtitle><description>The results of a study on the photocatalytic activity of aqueous dispersions of Ni-doped CdS nanocrystals (NCs) covered with an amphiphilic polyelectrolyte (PE) shell,
i.e.
, a polycation (NC-PC) or polyanion (NC-PA), are presented for the first time. The H
2
evolution rate measured under identical conditions served as a measure of activity. The NC-PC and NC-PA samples were characterized by similar PE content (~40%) and monomodal size distribution. According to our calculations based on the NC dimensions and lattice parameters, about one macromolecule of the PE is required to stabilize one NC. The average hydrodynamic diameter of the NC-PC was found to be 1.5 times larger than that of the NC-PA due to the difference between their chemical structures and different abilities of ionogenic groups to dissociate. The photocatal ytic activity of the PE-stabilized CdS nanocrystals was significantly influenced by the type of the PE, while the H
2
evolution rate depended on the reducing medium used during the process. When the medium contained Na
2
S or when the PE-stabilized NCs were pretreated with Na
2
S, the effect of the shell type was more pronounced and the activity of NC-PA was 2 to 14 times higher than that of NC-PC.</description><subject>Catalytic activity</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Chemistry/Food Science</subject><subject>Dispersions</subject><subject>Hydrogen evolution</subject><subject>Hydrogen production</subject><subject>Inorganic Chemistry</subject><subject>Lattice parameters</subject><subject>Nanocrystals</subject><subject>Nickel</subject><subject>Organic Chemistry</subject><subject>Photocatalysis</subject><subject>Polyelectrolytes</subject><subject>Size distribution</subject><subject>Sodium sulfide</subject><issn>1066-5285</issn><issn>1573-9171</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1UctKBDEQHETB5wd4C3geTSfzPMriCwQP6jlkk45GdidjklXG7_FD7WUETx6SLoqq6oQqilPg58B5e5EAoBUlh64Uohel3CkOoG5l2UMLu4R505S16Or94jClN8656LruoPhehPWoo87-A5k2NHyeWHBMv28wbBKzPo0Ykw9D2tIL-8gGPQQTp5T1KjG6l37lv9Cy5cQMBYXBG6YHS2fGY1hNuEKTI4GMifmBja8hB1JrYkjyOtkYXpD4GOzGbEOYi2HNPnXGeFzsOdqFJ7_zqHi-vnpa3Jb3Dzd3i8v70khoctm5tl-6ilsjXdt0dYeIvbWOV0i4bSSCk7qvhQGDDmqwctk4qHqUrdEa5FFxNufSK-j7Kau3sIkDrVQCKt7wum4qUsGsMjGkFNGpMfq1jpMCrrZlqLkMRWWobRlKkkfMnkTa4QXjX_L_ph-lfZK9</recordid><startdate>20181001</startdate><enddate>20181001</enddate><creator>Kabachii, Yu. A.</creator><creator>Kochev, S. Yu</creator><creator>Alenichev, M. K.</creator><creator>Antonova, O. Yu</creator><creator>Sadagov, A. Yu</creator><creator>Valetskii, P. M.</creator><creator>Nadtochenko, V. A.</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20181001</creationdate><title>Comparative activity of aqueous dispersions of CdS nanocrystals stabilized by cationic and anionic polyelectrolytes in photocatalytic hydrogen production from water</title><author>Kabachii, Yu. A. ; Kochev, S. Yu ; Alenichev, M. K. ; Antonova, O. Yu ; Sadagov, A. Yu ; Valetskii, P. M. ; Nadtochenko, V. A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c316t-8f79bf40dc3f76858eee9ddf04e58e763e1f3a952c1cef151d3b6f149e37caa13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Catalytic activity</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Chemistry/Food Science</topic><topic>Dispersions</topic><topic>Hydrogen evolution</topic><topic>Hydrogen production</topic><topic>Inorganic Chemistry</topic><topic>Lattice parameters</topic><topic>Nanocrystals</topic><topic>Nickel</topic><topic>Organic Chemistry</topic><topic>Photocatalysis</topic><topic>Polyelectrolytes</topic><topic>Size distribution</topic><topic>Sodium sulfide</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kabachii, Yu. A.</creatorcontrib><creatorcontrib>Kochev, S. Yu</creatorcontrib><creatorcontrib>Alenichev, M. K.</creatorcontrib><creatorcontrib>Antonova, O. Yu</creatorcontrib><creatorcontrib>Sadagov, A. Yu</creatorcontrib><creatorcontrib>Valetskii, P. M.</creatorcontrib><creatorcontrib>Nadtochenko, V. A.</creatorcontrib><collection>CrossRef</collection><jtitle>Russian chemical bulletin</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kabachii, Yu. A.</au><au>Kochev, S. Yu</au><au>Alenichev, M. K.</au><au>Antonova, O. Yu</au><au>Sadagov, A. Yu</au><au>Valetskii, P. M.</au><au>Nadtochenko, V. A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparative activity of aqueous dispersions of CdS nanocrystals stabilized by cationic and anionic polyelectrolytes in photocatalytic hydrogen production from water</atitle><jtitle>Russian chemical bulletin</jtitle><stitle>Russ Chem Bull</stitle><date>2018-10-01</date><risdate>2018</risdate><volume>67</volume><issue>10</issue><spage>1803</spage><epage>1806</epage><pages>1803-1806</pages><issn>1066-5285</issn><eissn>1573-9171</eissn><abstract>The results of a study on the photocatalytic activity of aqueous dispersions of Ni-doped CdS nanocrystals (NCs) covered with an amphiphilic polyelectrolyte (PE) shell,
i.e.
, a polycation (NC-PC) or polyanion (NC-PA), are presented for the first time. The H
2
evolution rate measured under identical conditions served as a measure of activity. The NC-PC and NC-PA samples were characterized by similar PE content (~40%) and monomodal size distribution. According to our calculations based on the NC dimensions and lattice parameters, about one macromolecule of the PE is required to stabilize one NC. The average hydrodynamic diameter of the NC-PC was found to be 1.5 times larger than that of the NC-PA due to the difference between their chemical structures and different abilities of ionogenic groups to dissociate. The photocatal ytic activity of the PE-stabilized CdS nanocrystals was significantly influenced by the type of the PE, while the H
2
evolution rate depended on the reducing medium used during the process. When the medium contained Na
2
S or when the PE-stabilized NCs were pretreated with Na
2
S, the effect of the shell type was more pronounced and the activity of NC-PA was 2 to 14 times higher than that of NC-PC.</abstract><cop>New York</cop><pub>Springer US</pub><doi>10.1007/s11172-018-2292-3</doi><tpages>4</tpages></addata></record> |
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subjects | Catalytic activity Chemistry Chemistry and Materials Science Chemistry/Food Science Dispersions Hydrogen evolution Hydrogen production Inorganic Chemistry Lattice parameters Nanocrystals Nickel Organic Chemistry Photocatalysis Polyelectrolytes Size distribution Sodium sulfide |
title | Comparative activity of aqueous dispersions of CdS nanocrystals stabilized by cationic and anionic polyelectrolytes in photocatalytic hydrogen production from water |
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