Photocatalytic Activity of Core/Shell Semiconductor Nanocrystals Featuring Spatial Separation of Charges
The present study investigates the photocatalytic activity of ZnSe/CdS core/shell semiconductor nanocrystals. These nanoparticles exhibit a spatial separation of photoinduced charges between the core and the shell domains, which makes them potentially viable for photocatalytic applications. Unfortun...
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Veröffentlicht in: | Journal of physical chemistry. C 2012-11, Vol.116 (43), p.22786-22793 |
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container_title | Journal of physical chemistry. C |
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creator | Perera, Dimuthu Lorek, Ryan Khnayzer, Rony S Moroz, Pavel O’Connor, Timothy Khon, Dmitry Diederich, Geoffrey Kinder, Erich Lambright, Scott Castellano, Felix N Zamkov, Mikhail |
description | The present study investigates the photocatalytic activity of ZnSe/CdS core/shell semiconductor nanocrystals. These nanoparticles exhibit a spatial separation of photoinduced charges between the core and the shell domains, which makes them potentially viable for photocatalytic applications. Unfortunately, one of the excited charges remains inside the core semiconductor and thus cannot efficiently react with the external environment. Here, we explore this issue by investigating the mechanisms of hole extraction from the ZnSe core to the surface of the CdS shell. In particular, the effect of shell thickness in ZnSe/CdS core/shell nanocrystals on the ability of core-localized charges to perform oxidative reactions was determined. By using a combination of time-resolved spectroscopy and electrochemical techniques, we demonstrate that the use of hole-scavenging surfactants facilitates an efficient transfer of core-localized holes to the surface even in the case of shells exceeding 7 nm in thickness. These measurements further demonstrate that photoinduced holes can be extracted from the core faster than they recombine with shell-localized electrons, indicating that most of the absorbed energy in ZnSe/CdS nanocrystals can be used to drive catalytic reactions. |
doi_str_mv | 10.1021/jp308921s |
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These nanoparticles exhibit a spatial separation of photoinduced charges between the core and the shell domains, which makes them potentially viable for photocatalytic applications. Unfortunately, one of the excited charges remains inside the core semiconductor and thus cannot efficiently react with the external environment. Here, we explore this issue by investigating the mechanisms of hole extraction from the ZnSe core to the surface of the CdS shell. In particular, the effect of shell thickness in ZnSe/CdS core/shell nanocrystals on the ability of core-localized charges to perform oxidative reactions was determined. By using a combination of time-resolved spectroscopy and electrochemical techniques, we demonstrate that the use of hole-scavenging surfactants facilitates an efficient transfer of core-localized holes to the surface even in the case of shells exceeding 7 nm in thickness. These measurements further demonstrate that photoinduced holes can be extracted from the core faster than they recombine with shell-localized electrons, indicating that most of the absorbed energy in ZnSe/CdS nanocrystals can be used to drive catalytic reactions.</description><identifier>ISSN: 1932-7447</identifier><identifier>EISSN: 1932-7455</identifier><identifier>DOI: 10.1021/jp308921s</identifier><language>eng</language><publisher>Columbus, OH: American Chemical Society</publisher><subject>Catalysis ; Catalysts: preparations and properties ; Chemistry ; Condensed matter: structure, mechanical and thermal properties ; Cross-disciplinary physics: materials science; rheology ; Exact sciences and technology ; General and physical chemistry ; Low-dimensional structures (superlattices, quantum well structures, multilayers): structure, and nonelectronic properties ; Materials science ; Nanopowders ; Nanoscale materials and structures: fabrication and characterization ; Physics ; Surfaces and interfaces; thin films and whiskers (structure and nonelectronic properties) ; Theory of reactions, general kinetics. 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C</title><addtitle>J. Phys. Chem. C</addtitle><description>The present study investigates the photocatalytic activity of ZnSe/CdS core/shell semiconductor nanocrystals. These nanoparticles exhibit a spatial separation of photoinduced charges between the core and the shell domains, which makes them potentially viable for photocatalytic applications. Unfortunately, one of the excited charges remains inside the core semiconductor and thus cannot efficiently react with the external environment. Here, we explore this issue by investigating the mechanisms of hole extraction from the ZnSe core to the surface of the CdS shell. In particular, the effect of shell thickness in ZnSe/CdS core/shell nanocrystals on the ability of core-localized charges to perform oxidative reactions was determined. By using a combination of time-resolved spectroscopy and electrochemical techniques, we demonstrate that the use of hole-scavenging surfactants facilitates an efficient transfer of core-localized holes to the surface even in the case of shells exceeding 7 nm in thickness. These measurements further demonstrate that photoinduced holes can be extracted from the core faster than they recombine with shell-localized electrons, indicating that most of the absorbed energy in ZnSe/CdS nanocrystals can be used to drive catalytic reactions.</description><subject>Catalysis</subject><subject>Catalysts: preparations and properties</subject><subject>Chemistry</subject><subject>Condensed matter: structure, mechanical and thermal properties</subject><subject>Cross-disciplinary physics: materials science; rheology</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>Low-dimensional structures (superlattices, quantum well structures, multilayers): structure, and nonelectronic properties</subject><subject>Materials science</subject><subject>Nanopowders</subject><subject>Nanoscale materials and structures: fabrication and characterization</subject><subject>Physics</subject><subject>Surfaces and interfaces; thin films and whiskers (structure and nonelectronic properties)</subject><subject>Theory of reactions, general kinetics. 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C</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Perera, Dimuthu</au><au>Lorek, Ryan</au><au>Khnayzer, Rony S</au><au>Moroz, Pavel</au><au>O’Connor, Timothy</au><au>Khon, Dmitry</au><au>Diederich, Geoffrey</au><au>Kinder, Erich</au><au>Lambright, Scott</au><au>Castellano, Felix N</au><au>Zamkov, Mikhail</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Photocatalytic Activity of Core/Shell Semiconductor Nanocrystals Featuring Spatial Separation of Charges</atitle><jtitle>Journal of physical chemistry. C</jtitle><addtitle>J. Phys. Chem. C</addtitle><date>2012-11-01</date><risdate>2012</risdate><volume>116</volume><issue>43</issue><spage>22786</spage><epage>22793</epage><pages>22786-22793</pages><issn>1932-7447</issn><eissn>1932-7455</eissn><abstract>The present study investigates the photocatalytic activity of ZnSe/CdS core/shell semiconductor nanocrystals. These nanoparticles exhibit a spatial separation of photoinduced charges between the core and the shell domains, which makes them potentially viable for photocatalytic applications. Unfortunately, one of the excited charges remains inside the core semiconductor and thus cannot efficiently react with the external environment. Here, we explore this issue by investigating the mechanisms of hole extraction from the ZnSe core to the surface of the CdS shell. In particular, the effect of shell thickness in ZnSe/CdS core/shell nanocrystals on the ability of core-localized charges to perform oxidative reactions was determined. By using a combination of time-resolved spectroscopy and electrochemical techniques, we demonstrate that the use of hole-scavenging surfactants facilitates an efficient transfer of core-localized holes to the surface even in the case of shells exceeding 7 nm in thickness. These measurements further demonstrate that photoinduced holes can be extracted from the core faster than they recombine with shell-localized electrons, indicating that most of the absorbed energy in ZnSe/CdS nanocrystals can be used to drive catalytic reactions.</abstract><cop>Columbus, OH</cop><pub>American Chemical Society</pub><doi>10.1021/jp308921s</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Catalysis Catalysts: preparations and properties Chemistry Condensed matter: structure, mechanical and thermal properties Cross-disciplinary physics: materials science rheology Exact sciences and technology General and physical chemistry Low-dimensional structures (superlattices, quantum well structures, multilayers): structure, and nonelectronic properties Materials science Nanopowders Nanoscale materials and structures: fabrication and characterization Physics Surfaces and interfaces thin films and whiskers (structure and nonelectronic properties) Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry |
title | Photocatalytic Activity of Core/Shell Semiconductor Nanocrystals Featuring Spatial Separation of Charges |
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