Photocatalytic hydrogen production from water-methanol mixtures using n-doped Sr2Nb2O7 under visible light irradiation: effects of catalyst structure
Nitrogen-doped perovskite type materials, Sr2Nb2O7-xNx (0, 1.5 < x < 2.8), have been studied as visible light-active photocatalysts for hydrogen production from methanol-water mixtures. Nitrogen doping in Sr2Nb2O7 red-shifted the light absorption edge into the visible light range and induced v...
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description | Nitrogen-doped perovskite type materials, Sr2Nb2O7-xNx (0, 1.5 < x < 2.8), have been studied as visible light-active photocatalysts for hydrogen production from methanol-water mixtures. Nitrogen doping in Sr2Nb2O7 red-shifted the light absorption edge into the visible light range and induced visible light photocatalytic activity. There existed an optimum amount of nitrogen doping that showed the maximum rate of hydrogen production. Among the potential variables that might cause this activity variation, the crystal structure appeared to be the most important. Thus, as the extent of N-doping increased, the original orthorhombic structure of the layered perovskite was transformed into an unlayered cubic oxynitride structure. The most active catalytic phase was an intermediate phase still maintaining the original layered perovskite structure, but with a part of its oxygen replaced by nitrogen and oxygen vacancy to adjust the charge difference between oxygen and doped nitrogen. These experimental observations were explained by density functional theory calculations. Thus, in Sr2Nb2O7-xNx, N2p orbital was the main contributor to the top of the valence band, causing band gap narrowing while the bottom of conduction band due to Nb 4d orbital remained almost unchanged. |
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Nitrogen doping in Sr2Nb2O7 red-shifted the light absorption edge into the visible light range and induced visible light photocatalytic activity. There existed an optimum amount of nitrogen doping that showed the maximum rate of hydrogen production. Among the potential variables that might cause this activity variation, the crystal structure appeared to be the most important. Thus, as the extent of N-doping increased, the original orthorhombic structure of the layered perovskite was transformed into an unlayered cubic oxynitride structure. The most active catalytic phase was an intermediate phase still maintaining the original layered perovskite structure, but with a part of its oxygen replaced by nitrogen and oxygen vacancy to adjust the charge difference between oxygen and doped nitrogen. These experimental observations were explained by density functional theory calculations. Thus, in Sr2Nb2O7-xNx, N2p orbital was the main contributor to the top of the valence band, causing band gap narrowing while the bottom of conduction band due to Nb 4d orbital remained almost unchanged.</description><identifier>ISSN: 1463-9076</identifier><identifier>EISSN: 1463-9084</identifier><identifier>DOI: 10.1039/b417052k</identifier><identifier>PMID: 19791350</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Calcium Compounds - chemistry ; Catalysis ; Chemistry ; Chemistry, Physical - methods ; Electric Conductivity ; Exact sciences and technology ; General and physical chemistry ; Hydrogen - chemistry ; Light ; Methanol - chemistry ; Nitrogen - chemistry ; Oxides - chemistry ; Oxygen - chemistry ; Photochemistry ; Photochemistry - methods ; Physical chemistry of induced reactions (with radiations, particles and ultrasonics) ; Strontium - chemistry ; Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry ; Titanium - chemistry ; Water - chemistry</subject><ispartof>Physical chemistry chemical physics : PCCP, 2005-03, Vol.7 (6), p.1315-1321</ispartof><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16657698$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19791350$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>SANG MIN JI</creatorcontrib><creatorcontrib>BORSE, Pramod H</creatorcontrib><creatorcontrib>HYUN GYU KIM</creatorcontrib><creatorcontrib>DONG WON HWANG</creatorcontrib><creatorcontrib>JUM SUK JANG</creatorcontrib><creatorcontrib>SANG WON BAE</creatorcontrib><creatorcontrib>JAE SUNG LEE</creatorcontrib><title>Photocatalytic hydrogen production from water-methanol mixtures using n-doped Sr2Nb2O7 under visible light irradiation: effects of catalyst structure</title><title>Physical chemistry chemical physics : PCCP</title><addtitle>Phys Chem Chem Phys</addtitle><description>Nitrogen-doped perovskite type materials, Sr2Nb2O7-xNx (0, 1.5 < x < 2.8), have been studied as visible light-active photocatalysts for hydrogen production from methanol-water mixtures. Nitrogen doping in Sr2Nb2O7 red-shifted the light absorption edge into the visible light range and induced visible light photocatalytic activity. There existed an optimum amount of nitrogen doping that showed the maximum rate of hydrogen production. Among the potential variables that might cause this activity variation, the crystal structure appeared to be the most important. Thus, as the extent of N-doping increased, the original orthorhombic structure of the layered perovskite was transformed into an unlayered cubic oxynitride structure. The most active catalytic phase was an intermediate phase still maintaining the original layered perovskite structure, but with a part of its oxygen replaced by nitrogen and oxygen vacancy to adjust the charge difference between oxygen and doped nitrogen. These experimental observations were explained by density functional theory calculations. Thus, in Sr2Nb2O7-xNx, N2p orbital was the main contributor to the top of the valence band, causing band gap narrowing while the bottom of conduction band due to Nb 4d orbital remained almost unchanged.</description><subject>Calcium Compounds - chemistry</subject><subject>Catalysis</subject><subject>Chemistry</subject><subject>Chemistry, Physical - methods</subject><subject>Electric Conductivity</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>Hydrogen - chemistry</subject><subject>Light</subject><subject>Methanol - chemistry</subject><subject>Nitrogen - chemistry</subject><subject>Oxides - chemistry</subject><subject>Oxygen - chemistry</subject><subject>Photochemistry</subject><subject>Photochemistry - methods</subject><subject>Physical chemistry of induced reactions (with radiations, particles and ultrasonics)</subject><subject>Strontium - chemistry</subject><subject>Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry</subject><subject>Titanium - chemistry</subject><subject>Water - chemistry</subject><issn>1463-9076</issn><issn>1463-9084</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkMlKBDEURYMozuAXSDa6K82cijsRJxAV1HWTytAdraq0SUrtD_F_LbHV1buLw7ncB8AeRkcYUXXcMCwRJy8rYBMzQSuFarb6l6XYAFs5PyOEMMd0HWxgJRWmHG2Cz_tZLNHoottFCQbOFjbFqevhPEU7mBJiD32KHXzXxaWqc2Wm-9jCLnyUIbkMhxz6KewrG-fOwodEbhtyJ-HQW5fgW8ihaR1sw3RWYEhJ26C_nSfQee9MyTB6-NOeC8wljZWjdgesed1mt7u82-Dp4vzx7Kq6ubu8Pju9qeaEq1KxxgusudA1kZZ4hg2tqVCWCWZqrwQliNQYSS6c4po1nFJuiFe8Fogyoug2OPzxjmtfB5fLpAvZuLbVvYtDnggpCJY1H8H9JTg0nbOTeQqdTovJ7yNH4GAJ6Gx065PuTcj_nBBcClXTL1cEgvI</recordid><startdate>20050321</startdate><enddate>20050321</enddate><creator>SANG MIN JI</creator><creator>BORSE, Pramod H</creator><creator>HYUN GYU KIM</creator><creator>DONG WON HWANG</creator><creator>JUM SUK JANG</creator><creator>SANG WON BAE</creator><creator>JAE SUNG LEE</creator><general>Royal Society of Chemistry</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20050321</creationdate><title>Photocatalytic hydrogen production from water-methanol mixtures using n-doped Sr2Nb2O7 under visible light irradiation: effects of catalyst structure</title><author>SANG MIN JI ; BORSE, Pramod H ; HYUN GYU KIM ; DONG WON HWANG ; JUM SUK JANG ; SANG WON BAE ; JAE SUNG LEE</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p259t-4bf61a56a827d2f41c38369d464c8f963202810756e95a4b5335c2f9586034293</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Calcium Compounds - chemistry</topic><topic>Catalysis</topic><topic>Chemistry</topic><topic>Chemistry, Physical - methods</topic><topic>Electric Conductivity</topic><topic>Exact sciences and technology</topic><topic>General and physical chemistry</topic><topic>Hydrogen - chemistry</topic><topic>Light</topic><topic>Methanol - chemistry</topic><topic>Nitrogen - chemistry</topic><topic>Oxides - chemistry</topic><topic>Oxygen - chemistry</topic><topic>Photochemistry</topic><topic>Photochemistry - methods</topic><topic>Physical chemistry of induced reactions (with radiations, particles and ultrasonics)</topic><topic>Strontium - chemistry</topic><topic>Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry</topic><topic>Titanium - chemistry</topic><topic>Water - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SANG MIN JI</creatorcontrib><creatorcontrib>BORSE, Pramod H</creatorcontrib><creatorcontrib>HYUN GYU KIM</creatorcontrib><creatorcontrib>DONG WON HWANG</creatorcontrib><creatorcontrib>JUM SUK JANG</creatorcontrib><creatorcontrib>SANG WON BAE</creatorcontrib><creatorcontrib>JAE SUNG LEE</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Physical chemistry chemical physics : PCCP</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SANG MIN JI</au><au>BORSE, Pramod H</au><au>HYUN GYU KIM</au><au>DONG WON HWANG</au><au>JUM SUK JANG</au><au>SANG WON BAE</au><au>JAE SUNG LEE</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Photocatalytic hydrogen production from water-methanol mixtures using n-doped Sr2Nb2O7 under visible light irradiation: effects of catalyst structure</atitle><jtitle>Physical chemistry chemical physics : PCCP</jtitle><addtitle>Phys Chem Chem Phys</addtitle><date>2005-03-21</date><risdate>2005</risdate><volume>7</volume><issue>6</issue><spage>1315</spage><epage>1321</epage><pages>1315-1321</pages><issn>1463-9076</issn><eissn>1463-9084</eissn><abstract>Nitrogen-doped perovskite type materials, Sr2Nb2O7-xNx (0, 1.5 < x < 2.8), have been studied as visible light-active photocatalysts for hydrogen production from methanol-water mixtures. Nitrogen doping in Sr2Nb2O7 red-shifted the light absorption edge into the visible light range and induced visible light photocatalytic activity. There existed an optimum amount of nitrogen doping that showed the maximum rate of hydrogen production. Among the potential variables that might cause this activity variation, the crystal structure appeared to be the most important. Thus, as the extent of N-doping increased, the original orthorhombic structure of the layered perovskite was transformed into an unlayered cubic oxynitride structure. The most active catalytic phase was an intermediate phase still maintaining the original layered perovskite structure, but with a part of its oxygen replaced by nitrogen and oxygen vacancy to adjust the charge difference between oxygen and doped nitrogen. These experimental observations were explained by density functional theory calculations. Thus, in Sr2Nb2O7-xNx, N2p orbital was the main contributor to the top of the valence band, causing band gap narrowing while the bottom of conduction band due to Nb 4d orbital remained almost unchanged.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><pmid>19791350</pmid><doi>10.1039/b417052k</doi><tpages>7</tpages></addata></record> |
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subjects | Calcium Compounds - chemistry Catalysis Chemistry Chemistry, Physical - methods Electric Conductivity Exact sciences and technology General and physical chemistry Hydrogen - chemistry Light Methanol - chemistry Nitrogen - chemistry Oxides - chemistry Oxygen - chemistry Photochemistry Photochemistry - methods Physical chemistry of induced reactions (with radiations, particles and ultrasonics) Strontium - chemistry Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry Titanium - chemistry Water - chemistry |
title | Photocatalytic hydrogen production from water-methanol mixtures using n-doped Sr2Nb2O7 under visible light irradiation: effects of catalyst structure |
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