光催化
红外线的
等离子体子
太阳能
材料科学
太阳能转换
光电子学
纳米技术
光化学
化学
催化作用
光学
物理
生态学
生物
生物化学
作者
Jiabin Cui,Yongjia Li,Lei Liu,Lin Chen,Jun Xu,Jingwen Ma,Gang Fang,Enbo Zhu,Hao Wu,Lixia Zhao,Leyu Wang,Yu Huang
出处
期刊:Nano Letters
[American Chemical Society]
日期:2015-09-07
卷期号:15 (10): 6295-6301
被引量:258
标识
DOI:10.1021/acs.nanolett.5b00950
摘要
We report a highly efficient photocatalyst comprised of Cu7S4@Pd heteronanostructures with plasmonic absorption in the near-infrared (NIR)-range. Our results indicated that the strong NIR plasmonic absorption of Cu7S4@Pd facilitated hot carrier transfer from Cu7S4 to Pd, which subsequently promoted the catalytic reactions on Pd metallic surface. We confirmed such enhancement mechanism could effectively boost the sunlight utilization in a wide range of photocatalytic reactions, including the Suzuki coupling reaction, hydrogenation of nitrobenzene, and oxidation of benzyl alcohol. Even under irradiation at 1500 nm with low power density (0.45 W/cm2), these heteronanostructures demonstrated excellent catalytic activities. Under solar illumination with power density as low as 40 mW/cm2, nearly 80–100% of conversion was achieved within 2 h for all three types of organic reactions. Furthermore, recycling experiments showed the Cu7S4@Pd were stable and could retain their structures and high activity after five cycles. The reported synthetic protocol can be easily extended to other Cu7S4@M (M = Pt, Ag, Au) catalysts, offering a new solution to design and fabricate highly effective photocatalysts with broad material choices for efficient conversion of solar energy to chemical energy in an environmentally friendly manner.
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