光催化
材料科学
X射线光电子能谱
异质结
纳米颗粒
化学工程
光电流
吸收边
静电纺丝
介电谱
纳米复合材料
氧烷
纳米技术
催化作用
电化学
带隙
光谱学
电极
复合材料
化学
有机化学
光电子学
物理化学
工程类
聚合物
物理
量子力学
作者
Karthikeyan Sekar,Chitiphon Chuaicham,Vellaichamy Balakumar,Wei Li,Wei Zhuang,Xiaohua Lü,Bunsho Ohtani,Keiko Sasaki
标识
DOI:10.1016/j.apcatb.2021.120221
摘要
• Cubic Cu2O (20-−100 nm) synthesis on TiO2 nanofiber. • Cube-on-nanofiber showed excellent photocatalytic H2 production and sulfamethoxazole decomposition. • Surface modified TiO2 confirmed by the energy-resolved distribution of electron traps (ERDT). • Heterojunction interfaces between cube-on-nanofiber promote charge transfer and provide active sites. We report a simple strategy for providing a homogenous TiO 2 nanofibre host environment to stabilize Cu 2 O nanoparticles with an average size of ∼60 nm and high dispersibility. We found that the small fraction of Cu 2 O nanoparticles in direct contact/partially submerged with TiO 2 nanofibre arrays (diameter ∼300 nm and length ∼650 nm) showed excellent synergistic photocatalytic performance for H 2 production rate of 48 μmol g −1 h -1 with an apparent quantum efficiency of 3.6 %. The H 2 production rate was much higher (factor of ∼6.5 times) compared with unmodified TiO 2 -NF. In addition, the synergistic Cu 2 O/TiO 2 -NF photocatalyst showed significant oxidative-degradation of sulfamethoxazole (7 × 10 -2 mmol g −1 min -1 ) and was highly stable during five cycles. The small fraction of Cu 2 O nanoparticles are well dispersed and form heterojunction interfaces to promote charge transfer and provide active sites. This argument is verified by morphology characterisation, band alignment, energy-resolved distribution of electron traps, electrochemical transient photocurrent, and electrochemical impedance (EIS). In addition, a detailed discussion is provided regarding the surface and bulk elemental composition determined by X-ray photoelectron spectroscopy (XPS), X-ray fluorescence (XRF), and X-ray absorption near edge structure (XANES).
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