光催化
可见光谱
催化作用
分解水
光化学
材料科学
人工光合作用
电子供体
制氢
纳米技术
化学
光电子学
生物化学
作者
Li J. Zhang,Shuo Li,Bing K. Liu,De J. Wang,Teng Xie
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2014-09-22
卷期号:4 (10): 3724-3729
被引量:650
摘要
Natural photosynthesis is usually recognized as an efficient mechanism to achieve solar energy conversion. We construct a CdS/WO3 nanojunction achieving a Z-scheme for clean hydrogen fuel evolution by mimicking the natural photosynthesis. Although WO3 alone cannot be used for H2 evolution from water splitting, it can significantly increase the H2 evolution activity of CdS through a Z-scheme mechanism with lactate as electron donor. The CdS/WO3 photocatalyst has a high H2 evolution rate of 369 μmol g–1 h–1 at a CdS concentration of 20 wt %, which is 5 times as high as that of CdS with lactic acid as electron donor. For further improving the hydrogen production rate, we introduce the noble metal Pt to ameliorate the charge transport between CdS and WO3. Good H2 evolution rates up to 2900 μmol g–1 h–1 were obtained with WPC3, which is about 7.9 times the rate of WC20 with visible radiation. The interesting thing is that the photocatalytic mechanism of CdS/WO3 is different from the previously reported mechanism. The results of TPV (transient photovoltage) and SPV (surface photovoltage) indicate that the Z-scheme system of CdS/WO3 can effectively promote charge separation and depress the charges recombining of photogenerated charge in CdS, based on the Z-scheme mechanism, resulting in efficient H2 production activity under visible light.
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