Surface-Functionalized Au–Pd Nanorods with Enhanced Photothermal Conversion and Catalytic Performance

纳米棒 材料科学 光热治疗 催化作用 化学工程 光热效应 纳米技术 双金属片 反应速率 金属 有机化学 化学 工程类 冶金
作者
Yuhang Zhao,Radwan M. Sarhan,Alberto Eljarrat,Zdravko Kochovski,Christoph T. Koch,Bernd Schmidt,Wouter Koopman,Yan Lü
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:14 (15): 17259-17272 被引量:20
标识
DOI:10.1021/acsami.2c00221
摘要

Bimetallic nanostructures comprising plasmonic and catalytic components have recently emerged as a promising approach to generate a new type of photo-enhanced nanoreactors. Most designs however concentrate on plasmon-induced charge separation, leaving photo-generated heat as a side product. This work presents a photoreactor based on Au-Pd nanorods with an optimized photothermal conversion, which aims to effectively utilize the photo-generated heat to increase the rate of Pd-catalyzed reactions. Dumbbell-shaped Au nanorods were fabricated via a seed-mediated growth method using binary surfactants. Pd clusters were selectively grown at the tips of the Au nanorods, using the zeta potential as a new synthetic parameter to indicate the surfactant remaining on the nanorod surface. The photothermal conversion of the Au-Pd nanorods was improved with a thin layer of polydopamine (PDA) or TiO2. As a result, a 60% higher temperature increment of the dispersion compared to that for bare Au rods at the same light intensity and particle density could be achieved. The catalytic performance of the coated particles was then tested using the reduction of 4-nitrophenol as the model reaction. Under light, the PDA-coated Au-Pd nanorods exhibited an improved catalytic activity, increasing the reaction rate by a factor 3. An analysis of the activation energy confirmed the photoheating effect to be the dominant mechanism accelerating the reaction. Thus, the increased photothermal heating is responsible for the reaction acceleration. Interestingly, the same analysis shows a roughly 10% higher reaction rate for particles under illumination compared to under dark heating, possibly implying a crucial role of localized heat gradients at the particle surface. Finally, the coating thickness was identified as an essential parameter determining the photothermal conversion efficiency and the reaction acceleration.

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