Xi Jiangbo, Huang Jie, Wang Deng, Wen Liangsong, Hao Jufang, He Baojiang, Chen Jun, Bai Zheng-Wu
School of Chemistry and Environmental Engineering, Key Laboratory of Green Chemical Engineering Process of Ministry of Education, Wuhan Institute of Technology, Wuhan 430073, China.
Ministry-of-Education Key Laboratory for the Green Preparation and Application of Functional Materials, Hubei University, Wuhan 430062, China.
J Phys Chem Lett. 2021 Apr 8;12(13):3443-3448. doi: 10.1021/acs.jpclett.1c00373. Epub 2021 Mar 31.
Exploring highly efficient catalysts with excellent photothermal conversion and further unveiling their catalytic mechanism are of significant importance for photothermal catalysis technologies, but there remain grand challenges to these activities. Herein, we fabricate a nest-like photothermal nanocatalyst with Pd decorated on a N-doped carbon functionalized BiS nanosphere (BiS@NC@Pd). Given its well-dispersed ultrafine Pd nanoparticles and the excellent photothermal heating ability of support material, the BiS@NC@Pd composite exhibits a superior activity and photothermal conversion property to commercial Pd/C catalyst for hydrogenation of organic dyes upon exposure to near-infrared (NIR) light irradiation. In addition, the photothermal effect (temperature rise) and activity enhancement of the heterogeneous catalysis system are further probed by comparing the reaction rate with and without the NIR light irradiation. Furthermore, the catalytic behaviors of the BiS@NC@Pd catalyst under conventional and photothermal heating are investigated at the same reaction temperature. This work not only improves our fundamental understanding of the catalytic behavior in heterogeneous liquid-solid reaction systems under near-infrared irradiation but also may promote the design of catalysts with photothermally promoted activity.
探索具有优异光热转换性能的高效催化剂并进一步揭示其催化机理对光热催化技术至关重要,但这些研究仍面临巨大挑战。在此,我们制备了一种巢状光热纳米催化剂,即在氮掺杂碳功能化的BiS纳米球(BiS@NC)上负载Pd(BiS@NC@Pd)。鉴于其分散良好的超细Pd纳米颗粒以及载体材料出色的光热加热能力,BiS@NC@Pd复合材料在近红外(NIR)光照射下对有机染料加氢反应表现出优于商业Pd/C催化剂的活性和光热转换性能。此外,通过比较有无近红外光照射时的反应速率,进一步探究了多相催化体系的光热效应(温度升高)和活性增强情况。此外,在相同反应温度下研究了BiS@NC@Pd催化剂在常规加热和光热加热条件下的催化行为。这项工作不仅增进了我们对近红外照射下多相液-固反应体系中催化行为的基本理解,还可能推动具有光热促进活性的催化剂设计。