Simultaneous production of hydrogen with the degradation of organic pollutants using TiO2 photocatalyst modified with dual surface components

光催化 催化作用 化学 降级(电信) 制氢 无机化学 金属 尿素 贵金属 锐钛矿 核化学 化学工程 有机化学 计算机科学 电信 工程类
作者
Jungwon Kim,Damián Monllor-Satoca,Wonyong Choi
出处
期刊:Energy and Environmental Science [The Royal Society of Chemistry]
卷期号:5 (6): 7647-7647 被引量:230
标识
DOI:10.1039/c2ee21310a
摘要

The simultaneous production of hydrogen and degradation of organic pollutants (4-chlorophenol, urea, and urine) was successfully achieved using titania photocatalysts which were modified with both anion adsorbates (fluoride or phosphate) and (noble) metals (Pt, Pd, Au, Ag, Cu, or Ni). The dual-function photocatalysis worked only when both components coexisted on the surface of TiO2, whereas TiO2 modified with a single surface component (F–TiO2, P–TiO2, or Pt/TiO2) was inactive under the same experimental condition. Two main surface-modified photocatalysts, F–TiO2/Pt (surface fluorinated and platinized) and P–TiO2/Pt (surface phosphated and platinized), were similarly active for dual-function photocatalysis in the anoxic suspension under UV irradiation. With these catalysts employed, the degradation of 4-chlorophenol (or urea) was accompanied by the concurrent production of H2. The synergistic effect greatly depended on the kind of metal and pH. The activity of F–TiO2/Pt gradually decreased with increasing pH, which makes the application of F–TiO2/Pt limited to the acidic pH region. On the other hand, P–TiO2/Pt exhibited a consistent activity over a wide range of pH, which makes P–TiO2/Pt a more practical dual-function photocatalyst. The synergistic effect of anions and metal deposits on the surface of TiO2 enhanced the interfacial electron transfer and reduced the charge recombination which resulted in a maximum of 20-fold increase of H2 production compared to metal deposited TiO2 in the presence of 4-chlorophenol.

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