光催化
原位
辐照
可见光谱
材料科学
过程(计算)
光化学
化学
光电子学
计算机科学
物理
生物化学
有机化学
催化作用
操作系统
核物理学
作者
Hui Pan,Feng Wang,Jianbing Huang,N CHEN
出处
期刊:Acta physico-chimica Sinica
[Acta Physico-Chimica Sinica & University Chemistry Editorial Office, Peking University]
日期:2008-06-01
卷期号:24 (6): 992-996
被引量:8
标识
DOI:10.1016/s1872-1508(08)60045-5
摘要
Abstract Cobalt phthalocyanine (CoPc) was synthesized and self-assembled on the surface of nanoscale tin dioxide (SnO2) by in-situ process, marked as i, and Co–O interaction was verified to conjugate axially between macromolecule (CoPc) and SnO2 in CoPc/SnO2(i). The results indicated that the binding constant of CoPc/SnO2(i) was two-order higher than that of CoPc/SnO2(d) synthesized by dipping process, marked as d, while the numbers of binding sites were comparable in both samples. The degradation rate in the photocatalytic activity of CoPc/SnO2(i) was 32.5% higher than that of CoPc/SnO2(d) under visible-light irradiation for 150 min due to the effective electron separation and energy injection from LUMO of CoPc to conduction band of SnO2 for CoPc/SnO2(i) based on the strong interaction between CoPc and SnO2. The degradation recyclability of CoPc/SnO2(i) retained 48.8% in 10 times under the same circular photocatalytic process.
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