Maity Niladri, Mishra Aman, Barman Samir, Padhi Sumanta Kumar, Panda Binod Bihari, Jaseer E A, Javid Mohamed
Interdisciplinary Research Center for Refining and Advanced Chemicals, King Fahd University of Petroleum & Minerals, Dhahran 31261, Saudi Arabia.
Artificial Photosynthesis Laboratory, Department of Chemistry and Chemical Biology, Indian Institute of Technology (Indian School of Mines), Dhanbad 826004, India.
ACS Omega. 2023 Dec 20;9(1):1020-1028. doi: 10.1021/acsomega.3c07246. eCollection 2024 Jan 9.
Fly ash (FA)-supported bimetallic nanoparticles (PdAg/FA) with varying Pd:Ag ratios were prepared by coprecipitation of Pd and Ag involving in situ reduction of Pd(II) and Ag(I) salts in aqueous medium. All the supported nanoparticles were thoroughly characterized with the aid of powder X-ray diffraction (PXRD), X-ray photoelectron spectroscopy (XPS), electron microscopy (field emission scanning electron microscopy (FE-SEM) and transmission electron microscopy (TEM)), and elemental analyses, which include inductively coupled plasma-optical emission spectroscopy (ICP-OES) and energy-dispersive X-ray spectroscopy (EDS). A gradual broadening and shifting of PXRD peaks, ascribable to Ag, to higher angles with an increase in the Pd:Ag ratio affirms the alloying of interface between Pd and Ag nanoparticles. The coexistence of Pd and Ag was further confirmed by EDS elemental mapping as well as by the presence of bimetallic lattices on the FA surface, as evident from the high-resolution TEM analysis. The dependency of crystallite size and average size of bimetallic nanoparticles on Ag loading (mol %) was elucidated with the help of a combination of PXRD and TEM studies. Based on XPS analysis, the charge transfer phenomenon between contacting Pd-Ag sites could be evident from the shifting of 3d core electron binding energy for both Pd and Ag compared with monometallic Pd and Ag nanoparticles. Following a pseudo-first-order reaction kinetics, all the nanocatalysts were able to efficiently reduce 4-nitrophenol into 4-aminophenol in aqueous NaBH. The superior catalytic performance of the bimetallic nanocatalysts (PdAg/FA) over their monometallic (Pd/FA and Ag/FA) analogues has been demonstrated. Moreover, the tunable synergistic effect of the bimetallic systems has been explored in detail by varying the Pd:Ag mol ratio in a systematic manner which in turn allowed us to achieve an optimum reaction rate ( = 1.050 min) for the nitrophenol reduction using a PdAg/FA system. Most importantly, all the bimetallic nanocatalysts explored here exhibited excellent normalized rate constants ( ≈ 6000-15,000 min mmol) compared with other supported bimetallic Pd-Ag nanocatalysts reported in the literature.
通过在水介质中原位还原钯(II)和银(I)盐,共沉淀钯和银制备了具有不同钯:银比例的粉煤灰(FA)负载双金属纳米颗粒(PdAg/FA)。借助粉末X射线衍射(PXRD)、X射线光电子能谱(XPS)、电子显微镜(场发射扫描电子显微镜(FE-SEM)和透射电子显微镜(TEM))以及元素分析(包括电感耦合等离子体发射光谱(ICP-OES)和能量色散X射线光谱(EDS))对所有负载型纳米颗粒进行了全面表征。随着钯:银比例的增加,归因于银的PXRD峰逐渐变宽并向更高角度移动,这证实了钯和银纳米颗粒之间界面的合金化。EDS元素映射以及FA表面双金属晶格的存在进一步证实了钯和银的共存,这从高分辨率TEM分析中可以明显看出。结合PXRD和TEM研究,阐明了双金属纳米颗粒的微晶尺寸和平均尺寸对银负载量(摩尔%)的依赖性。基于XPS分析,与单金属钯和银纳米颗粒相比,钯和银的3d核心电子结合能的移动表明了接触的钯-银位点之间的电荷转移现象。遵循准一级反应动力学,所有纳米催化剂都能够在水相硼氢化钠中有效地将4-硝基苯酚还原为4-氨基苯酚。已经证明了双金属纳米催化剂(PdAg/FA)比其单金属(Pd/FA和Ag/FA)类似物具有优异的催化性能。此外,通过系统地改变钯:银摩尔比,详细探索了双金属体系的可调协同效应,这反过来又使我们能够使用PdAg/FA体系实现硝基苯酚还原的最佳反应速率(k = 1.050 min⁻¹)。最重要的是,与文献中报道的其他负载型双金属钯-银纳米催化剂相比,这里探索的所有双金属纳米催化剂都表现出优异的归一化速率常数(k ≈ 6000 - 15,000 min⁻¹ mmol⁻¹)。