光催化
纳米棒
氧化还原
材料科学
热液循环
氢氧化物
离子
制作
化学工程
辐照
氧气
微观结构
析氧
纳米技术
催化作用
化学
电化学
物理化学
电极
冶金
医学
生物化学
物理
病理
有机化学
核物理学
替代医学
工程类
作者
Bao Zhong Dong,Lingyao Li,Zhifang Dong,Rong Xu,Yan Wu
标识
DOI:10.1016/j.ijhydene.2017.10.061
摘要
In this work, CeO2 NRs were synthesized by a hydrothermal approach and their microstructures were controlled by modifying the concentration of the hydroxide ions. The as-synthesized CeO2 NRs appeared highly crystallized with a cubic structure, while their lengths increased from ∼20 to 50 nm as the concentration of the hydroxide ions increased. By tuning their surface properties, the CeO2 NR samples exhibited favorable band structures, which enabled them to effectively absorb large amount of photon energies and enhance the photocatalytic properties. The optimum CeO2 sample showed the highest H2 production rate (∼25.10 μmol/g after solarlight irradiation for 5 h), largest Brunauer-Emmett-Teller specific surface area (65.26 m2/g), smallest pore size (7.0 nm), and largest amount of oxygen vacancies. The photocatalytic H2 evolution properties were attributed to the preferred planes of the CeO2 NRs and the redox capacity of CeO2. The photocatalytic process is mainly related to the conversion of Ce3+/Ce4+ cycle of CeO2, and the redox capability of CeO2 is related to the amount of its oxygen vacancies.
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