Zhu Jie, Lu Xiaoxue, Li Yijian, Li Tingdong, Yang Linsong, Yang Kun, Ji Liang, Lu Mohong, Li Mingshi
National-Local Joint Engineering Research Center of Biomass Refining and High-Quality Utilization, Changzhou University, Changzhou, 213164 China.
Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology, Changzhou University, Changzhou, 213164 China.
Catal Letters. 2020;150(12):3542-3552. doi: 10.1007/s10562-020-03252-6. Epub 2020 May 14.
In this work, a new viral protein cage based nanoreactor was successfully constructed via encapsulating Tween 80 stabilized palladium nanoparticles (NPs) into rotavirus capsid VP2 virus-like particles (i.e. Pd@VP2). The effects of stabilizers including CTAB, SDS, Tween 80 and PVP on controlling the particle size of Pd NPs were investigated. They were further immobilized on graphene oxide (i.e. Pd@VP2/GO) by a simple mixing method. Some characterizations including FT-IR and XPS were conducted to study adsorption mode of Pd@VP2 on GO sheets. Their catalytic performance was estimated in the reduction of 4-nitrophenol (4-NP). Results showed that Tween 80 stabilized Pd NPs with the molar ratio of Pd to Tween 80 at 1:0.1 possessed the smallest size and the best stability as well. They were encapsulated into viral protein cages (mean size 49 ± 0.26 nm) to assemble confined nanoreactors, most of which contained 1-2 Pd NPs (mean size 8.15 ± 0.26 nm). As-prepared Pd@VP2 indicated an enhanced activity (apparent reaction rate constant = (3.74 ± 0.10) × 10 s) for the reduction of 4-NP in comparison to non-confined Pd-Tween80 colloid ( = (2.20 ± 0.06) × 10 s). It was logically due to confinement effects of Pd@VP2 including high dispersion of Pd NPs and high effective concentration of substrates in confined space. Pd@VP2 were further immobilized on GO surface through C-N bond. Pd@VP2/GO exhibited good reusability after recycling for four runs, confirming the strong anchoring effects of GO on Pd@VP2.
在本工作中,通过将吐温80稳定的钯纳米颗粒(NPs)封装到轮状病毒衣壳VP2病毒样颗粒中(即Pd@VP2),成功构建了一种新型的基于病毒蛋白笼的纳米反应器。研究了包括十六烷基三甲基溴化铵(CTAB)、十二烷基硫酸钠(SDS)、吐温80和聚乙烯吡咯烷酮(PVP)在内的稳定剂对控制钯纳米颗粒粒径的影响。通过简单的混合方法将它们进一步固定在氧化石墨烯上(即Pd@VP2/GO)。进行了包括傅里叶变换红外光谱(FT-IR)和X射线光电子能谱(XPS)在内的一些表征,以研究Pd@VP2在氧化石墨烯片上的吸附模式。在对4-硝基苯酚(4-NP)的还原反应中评估了它们的催化性能。结果表明,钯与吐温80摩尔比为1:0.1时吐温80稳定的钯纳米颗粒尺寸最小且稳定性最佳。它们被封装到病毒蛋白笼(平均尺寸49±0.26 nm)中以组装受限纳米反应器,其中大部分包含1-2个钯纳米颗粒(平均尺寸8.15±0.26 nm)。与非受限的Pd-吐温80胶体(k =(2.20±0.06)×10⁻³ s⁻¹)相比,所制备的Pd@VP2对4-NP的还原显示出增强的活性(表观反应速率常数k =(3.74±0.10)×10⁻³ s⁻¹)。这在逻辑上归因于Pd@VP2的受限效应,包括钯纳米颗粒的高分散性和受限空间中底物的高有效浓度。Pd@VP2通过C-N键进一步固定在氧化石墨烯表面。Pd@VP2/GO在循环使用四次后表现出良好的可重复使用性,证实了氧化石墨烯对Pd@VP2的强锚固作用。