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Maximizing the visible light photoelectrochemical activity of B/N-doped anatase TiO2 microspheres with exposed dominant {001} facets
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dc.contributor.author | Hong, Xingxing | |
dc.contributor.author | Kang, Yuyang | |
dc.contributor.author | Zhen, Chao | |
dc.contributor.author | Kang, Xiangdong | |
dc.contributor.author | Yin, Li-Chang | |
dc.contributor.author | Irvine, John T. S. | |
dc.contributor.author | Wang, Lianzhou | |
dc.contributor.author | Liu, Gang | |
dc.contributor.author | Cheng, Hui-Ming | |
dc.date.accessioned | 2019-03-15T00:38:02Z | |
dc.date.available | 2019-03-15T00:38:02Z | |
dc.date.issued | 2018-06 | |
dc.identifier.citation | Hong , X , Kang , Y , Zhen , C , Kang , X , Yin , L-C , Irvine , J T S , Wang , L , Liu , G & Cheng , H-M 2018 , ' Maximizing the visible light photoelectrochemical activity of B/N-doped anatase TiO 2 microspheres with exposed dominant {001} facets ' , Science China Materials , vol. 61 , no. 6 , pp. 831-838 . https://doi.org/10.1007/s40843-018-9234-y | en |
dc.identifier.issn | 2199-4501 | |
dc.identifier.other | PURE: 252738071 | |
dc.identifier.other | PURE UUID: f1e78c25-d781-490d-b60a-387ed610ab0c | |
dc.identifier.other | RIS: urn:EC8939D91098BC60FC7834E707E8A3DB | |
dc.identifier.other | RIS: Hong2018 | |
dc.identifier.other | Scopus: 85045027099 | |
dc.identifier.other | WOS: 000432687500005 | |
dc.identifier.other | ORCID: /0000-0002-8394-3359/work/68280736 | |
dc.identifier.uri | https://hdl.handle.net/10023/17291 | |
dc.description | This work was supported by the Major Basic Research Program, Ministry of Science and Technology of China (2014CB239401), the National Natural Science Fundation of China (51422210, 21633009, 51629201 and 51521091), the Key Research Program of Frontier Sciences CAS (QYZDB-SSW-JSC039). Liu G thanks Newton Advanced Fellowship. | en |
dc.description.abstract | Anatase TiO2 microspheres with exposed dominant BBBBB001BBBBB facets were doped with interstitial boron to have a concentration gradient with the maximum concentration at the surface. They were then further doped with substitutional nitrogen by heating in an ammonia atmosphere at different temperatures from 440 to 560°C to give surface N concentrations ranging from 7.03 to 15.47 at%. The optical absorption, atomic and electronic structures and visible-light photoelectrochemical water oxidation activity of these materials were investigated. The maximum activity of the doped TiO2 was achieved at a nitrogen doping temperature of 520°C that gave a high absorbance over the whole visible light region but with no defect-related background absorption. | |
dc.format.extent | 8 | |
dc.language.iso | eng | |
dc.relation.ispartof | Science China Materials | en |
dc.rights | © Science China Press and Springer-Verlag GmbH Germany, part of Springer Nature 2018. This work has been made available online in accordance with the publisher’s policies. This is the author created, accepted version manuscript following peer review and may differ slightly from the final published version. The final published version of this work is available at https://doi.org/10.1007/s40843-018-9234-y | en |
dc.subject | Photoelectrochemistry | en |
dc.subject | Red TiO2 | en |
dc.subject | Water splitting | en |
dc.subject | Doping | en |
dc.subject | QD Chemistry | en |
dc.subject | NDAS | en |
dc.subject | SDG 7 - Affordable and Clean Energy | en |
dc.subject.lcc | QD | en |
dc.title | Maximizing the visible light photoelectrochemical activity of B/N-doped anatase TiO2 microspheres with exposed dominant {001} facets | en |
dc.type | Journal article | en |
dc.contributor.sponsor | The Royal Society | en |
dc.description.version | Postprint | en |
dc.description.version | Postprint | en |
dc.contributor.institution | University of St Andrews. School of Chemistry | en |
dc.contributor.institution | University of St Andrews. EaSTCHEM | en |
dc.identifier.doi | https://doi.org/10.1007/s40843-018-9234-y | |
dc.description.status | Peer reviewed | en |
dc.date.embargoedUntil | 2019-03-15 | |
dc.identifier.grantnumber | NA140077 | en |
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