High performance carbon/silica co-decorated TiO2 nanotubes for visible-light driven water splitting
- 1. Key Laboratory of Renewable Energy, Guangdong Provincial Key Laboratory of New and Renewable Energy Research and Development, Guangzhou Institute of Energy Conversion, Chinese Academy of Sciences, Guangzhou 510640 (China)
- 2. Low Carbon Energy Institute, School of Chemical Engineering & Technology, China University of Mining and Technology, Xuzhou, 221116 (China)
Description
Graphical abstract: Using amino-propyl-triethoxy silane (KH570) as silane couplers, a novel carbon/silica dots co-decorated TiO2 nanotube (CS@TNT) is prepared through silane modification and thermal calcination approach. The CS@TNT retains its tubular morphology at as high as 500 °C, and presents a high activity (0.096 mmol/h) towards photocatalytic water splitting. - Highlights: • A novel route of silane-modification then H2 calcination is developed. • Carbon and silica dots are highly dispersed on the TNT. • The CS@TNT retains its tubular morphology at as high as 500 °C. • A high activity (0.096 mmol/h) is achieved towards photocatalytic water splitting. • Effect of carbon/silica modification is investigated in detail. - Abstract: A novel carbon/silica co-decorated TiO2 nanotubes (TNT) photocatalyst (CS@TNT) was prepared for visible light driven water splitting by a facile two-steps process of amino-propyl-triethoxy silane modification and calcination. Structure characterizations (XRD, STEM, XPS, UV–vis spectra and PL spectra) revealed that the silica and carbon dots were homogeneously dispersed on the surfaces of TNT. The introduced silica resists crystallization of TNT, and keeps the tubular morphology intact and high surface area; the co-existence of carbon dots increases the visible light absorbance capacity and promotes the electron-hole separation efficiency. The CS@TNT preserves intact tubular morphology during calcination (500 °C), and a high activity of 0.096 mmol/h is achieved, which was 1.7 times higher than that of actual catalyst made of gold nanoparticles loading on TNT.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.materresbull.2017.04.042Additional details
Identifiers
- DOI
- 10.1016/j.materresbull.2017.04.042;
- PII
- S0025-5408(17)30671-2;
Publishing Information
- Journal Title
- Materials Research Bulletin
- Journal Volume
- 93
- Journal Page Range
- p. 162-169
- ISSN
- 0025-5408
- CODEN
- MRBUAC
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 49081326
- Subject category
- S36: MATERIALS SCIENCE;
- Descriptors DEI
- CALCINATION; CARBON MONOXIDE; CRYSTAL LATTICES; CRYSTALLIZATION; MODIFICATIONS; MORPHOLOGY; NANOTUBES; OXIDATION; SILANES; SILICA; SURFACE AREA; TITANIUM OXIDES; TNT; ULTRAVIOLET SPECTRA; VISIBLE SPECTRA; X-RAY DIFFRACTION; X-RAY PHOTOELECTRON SPECTROSCOPY
- Descriptors DEC
- CARBON COMPOUNDS; CARBON OXIDES; CHALCOGENIDES; CHEMICAL EXPLOSIVES; CHEMICAL REACTIONS; COHERENT SCATTERING; CRYSTAL STRUCTURE; DECOMPOSITION; DIFFRACTION; ELECTRON SPECTROSCOPY; EXPLOSIVES; HYDRIDES; HYDROGEN COMPOUNDS; MINERALS; NANOSTRUCTURES; NITRO COMPOUNDS; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; ORGANIC SILICON COMPOUNDS; OXIDE MINERALS; OXIDES; OXYGEN COMPOUNDS; PHASE TRANSFORMATIONS; PHOTOELECTRON SPECTROSCOPY; PYROLYSIS; SCATTERING; SILICON COMPOUNDS; SPECTRA; SPECTROSCOPY; SURFACE PROPERTIES; THERMOCHEMICAL PROCESSES; TITANIUM COMPOUNDS; TRANSITION ELEMENT COMPOUNDS
Optional Information
- Copyright
- Copyright (c) 2017 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.