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Efficient production of H2O2 on Au/WO3 under visible light and the influencing factors
Applied Catalysis B: Environment and Energy ( IF 22.1 ) Pub Date : 2020-11-25 , DOI: 10.1016/j.apcatb.2020.119691
Yechen Wang , Yaru Wang , Jianjun Zhao , Min Chen , Xubo Huang , Yiming Xu

Production of H2O2 via a more economic, green and safe way is challenging. In this work, we report an efficient production of H2O2 from oxygen reduction reaction (ORR) in aqueous solution over a modified WO3 with Au nanoparticles. Under visible light at wavelengths longer than 420 nm for 5 h, H2O2 measured from WO3 and Au/WO3 were 1.07, and 177 μM, respectively. On addition of methanol, H2O2 obtained from WO3, Au/WO3, and Au/SiO2 were 8.55, 544, and 0.36 μM, respectively. Photoluminescence and electrochemical measurement revealed that there was an interfacial electron transfer from the excited WO3 to Au, followed by two-electron reduction of O2 on Au sites. Under visible light at wavelengths longer than 535 nm, interestingly, H2O2 was also produced from Au/WO3 (39 μM at 5 h), while the photocurrent of water oxidation on Au/WO3 was much larger than those on Au/SiO2 and WO3. Clearly, there is also an interfacial electron transfer from the plasmonic Au to WO3, followed by ORR to H2O2, but such a process fails when WO3 is excited. However, the production of H2O2 on Au/WO3 was determined by several factors, including Au content, light absorption, and particle size. A maximum H2O2 was observed at an initial pH 3.0 from 0.35 wt% Au/WO3, prepared at 400 °C. Moreover, at the same loading on WO3, Au was more efficient than Pd, Ag, Pt, Ni, Cu, and Co, while at the same Au loading, WO3 was more efficient than BiVO4 and Bi2WO6. The superior performance of Au/WO3 is mainly due to its ability to undergo selective ORR to H2O2, and to release protons into aqueous solution protecting H2O2 from decomposition.



中文翻译:

可见光下Au / WO 3上H 2 O 2的高效生成及其影响因素

通过更经济,绿色和安全的方式生产H 2 O 2具有挑战性。在这项工作中,我们报告了在含Au纳米粒子的改性WO 3上,通过水溶液中的氧还原反应(ORR)可高效生产H 2 O 2。在波长大于420 nm的可见光下持续5 h,从WO 3和Au / WO 3测得的H 2 O 2分别为1.07和177μM。上加入甲醇,H 2 ö 2从WO得到3,金/ WO 3,和Au /二氧化硅2分别为8.55、544和0.36μM。光致发光和电化学测量表明,存在从激发的WO 3到Au的界面电子转移,然后在Au位点上O 2的两电子还原。有趣的是,在波长大于535 nm的可见光下,Au / WO 3(5 h时为39μM)也产生了H 2 O 2,而Au / WO 3上水氧化的光电流远大于Au上的/ SiO 2和WO 3。显然,还存在从等离子Au到WO 3的界面电子转移,然后是ORR到H 2 O 2的界面转移。但是,当WO 3被激发时,这样的过程失败。但是,Au / WO 3上H 2 O 2的产生取决于几个因素,包括Au含量,光吸收率和粒径。在400℃下制备的0.35重量%的Au / WO 3的初始pH 3.0下观察到最大的H 2 O 2。此外,在WO 3相同的负载下,Au比Pd,Ag,Pt,Ni,Cu和Co更有效,而在相同Au负载下,WO 3比BiVO 4和Bi 2 WO 6更有效。Au / WO 3的卓越性能这主要归因于其对H 2 O 2进行选择性ORR以及将质子释放到水溶液中以保护H 2 O 2免受分解的能力。

更新日期:2020-12-10
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