4.6 Article

Green Photocatalytic Oxidation of Benzyl Alcohol over Noble-Metal-Modified H2Ti3O7 Nanowires

期刊

ACS SUSTAINABLE CHEMISTRY & ENGINEERING
卷 7, 期 10, 页码 9717-9726

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acssuschemeng.9b01817

关键词

H2Ti3O7 nanowires; Noble metal nanoparticles; Benzyl alcohol; Benzaldehyde; Photocatalysis; Solvent-free

资金

  1. National Nature Science Foundation [21606198, 51728902]
  2. Natural Science Foundation of Zhejiang province [LQ16B060004, LGF18D060002]
  3. China Postdoctoral Science Foundation [2016M592014]

向作者/读者索取更多资源

One-dimensional H2Ti3O7 nanowires (NWs) supported by Au, Ag, and Pd monometallic nanoparticles (NPs) and Au-Pd bimetallic NPs were prepared and used for photochemical benzyl alcohol oxidation. Techniques, such as XRD, TEM, XPS, N-2 physisorption, and diffuse reflectance ultraviolet-visible (DRUV-vis), were used to characterize the obtained catalysts. These results showed that the Pd/H2Ti3O7 NWs catalyst under light irradiation displayed an enhanced photocatalytic performance, nearly 2.6 times higher than that for the catalyst without irradiation and about 1.5 times higher than that for Pd/TiO2(P25) with irradiation. The enhanced benzyl alcohol oxidation activity for Pd/H2Ti3O7 NWs might be due to the favorable synergetic effect between Pd and H(2)Ti(3)O(7 )NWs. Particularly, highly dispersed Pd NPs with about 10.2 nm on H2Ti3O7 NWs can promoted the light harvesting ability. The well-matched contact boundary between H2Ti3O7 NWs and Pd NPs might promote separation for the photoinduced electron and hole pairs. After S recycle utilization cycles, there was no evident decline in activity and selectivity for the Pd/H2Ti3O7 NVVs catalyst, which still maintained its original structure of H2Ti3O7 NWs. The current study provides a potential application in the green and highly efficient photocatalytic synthesis of other organic compounds and other environmental applications.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据