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Article: Controlled Synthesis of N-Doped Carbon Nanospheres with Tailored Mesopores through Self-Assembly of Colloidal Silica

TitleControlled Synthesis of N-Doped Carbon Nanospheres with Tailored Mesopores through Self-Assembly of Colloidal Silica
Authors
Keywordsmesoporous carbon
mesoporous polyaniline
nanospheres
nitrogen-doping
oxygen reduction reaction
Issue Date2015
Citation
Angewandte Chemie - International Edition, 2015, v. 54, n. 50, p. 15191-15196 How to Cite?
AbstractLimited strategies have been established to prepare monodisperse mesoporous carbon nanospheres (MCNs) with tailored pore sizes. In this work, a method is reported to synthesize MCNs by combining polymerization of aniline with co-assembly of colloidal silica nanoparticles. The controlled self-assembly behavior of colloidal silica enables the formation of uniform composite nanospheres and convenient modulation over mesopores. After carbonization and removal of sacrificial templates, the resultant MCNs possess tunable mesopores (7-42 nm) and spherical diameters (90-300 nm), as well as high surface area (785-1117 m2 g-1), large pore volume (1.46-2.01 cm3 g-1) and abundant nitrogen moieties (5.54-8.73 at %). When serving as metal-free electrocatalysts for the oxygen reduction reaction (ORR), MCNs with an optimum pore size of 22 nm, compared to those with 7 and 42 nm, exhibit the best ORR performance in alkaline medium. N-doped mesoporous carbon nanospheres (N-MCNs): A highly controlled self-assembly method based on colloidal silica was developed for the facile synthesis of N-MCNs with desired porous and chemical features (tunable mesopore size, high surface area, and N-doping content), which can serve as high-performance electrocatalysts for oxygen reduction reaction.
Persistent Identifierhttp://hdl.handle.net/10722/349105
ISSN
2023 Impact Factor: 16.1
2023 SCImago Journal Rankings: 5.300

 

DC FieldValueLanguage
dc.contributor.authorWang, Gang-
dc.contributor.authorSun, Yuhan-
dc.contributor.authorLi, Debao-
dc.contributor.authorLiang, Hai Wei-
dc.contributor.authorDong, Renhao-
dc.contributor.authorFeng, Xinliang-
dc.contributor.authorMüllen, Klaus-
dc.date.accessioned2024-10-17T06:56:18Z-
dc.date.available2024-10-17T06:56:18Z-
dc.date.issued2015-
dc.identifier.citationAngewandte Chemie - International Edition, 2015, v. 54, n. 50, p. 15191-15196-
dc.identifier.issn1433-7851-
dc.identifier.urihttp://hdl.handle.net/10722/349105-
dc.description.abstractLimited strategies have been established to prepare monodisperse mesoporous carbon nanospheres (MCNs) with tailored pore sizes. In this work, a method is reported to synthesize MCNs by combining polymerization of aniline with co-assembly of colloidal silica nanoparticles. The controlled self-assembly behavior of colloidal silica enables the formation of uniform composite nanospheres and convenient modulation over mesopores. After carbonization and removal of sacrificial templates, the resultant MCNs possess tunable mesopores (7-42 nm) and spherical diameters (90-300 nm), as well as high surface area (785-1117 m2 g-1), large pore volume (1.46-2.01 cm3 g-1) and abundant nitrogen moieties (5.54-8.73 at %). When serving as metal-free electrocatalysts for the oxygen reduction reaction (ORR), MCNs with an optimum pore size of 22 nm, compared to those with 7 and 42 nm, exhibit the best ORR performance in alkaline medium. N-doped mesoporous carbon nanospheres (N-MCNs): A highly controlled self-assembly method based on colloidal silica was developed for the facile synthesis of N-MCNs with desired porous and chemical features (tunable mesopore size, high surface area, and N-doping content), which can serve as high-performance electrocatalysts for oxygen reduction reaction.-
dc.languageeng-
dc.relation.ispartofAngewandte Chemie - International Edition-
dc.subjectmesoporous carbon-
dc.subjectmesoporous polyaniline-
dc.subjectnanospheres-
dc.subjectnitrogen-doping-
dc.subjectoxygen reduction reaction-
dc.titleControlled Synthesis of N-Doped Carbon Nanospheres with Tailored Mesopores through Self-Assembly of Colloidal Silica-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1002/anie.201507735-
dc.identifier.scopuseid_2-s2.0-84954429271-
dc.identifier.volume54-
dc.identifier.issue50-
dc.identifier.spage15191-
dc.identifier.epage15196-
dc.identifier.eissn1521-3773-

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