Jain Siddarth, Panigrahi Abhiram, Sarma Tridib K
Discipline of Chemistry, Indian Institute of Technology Indore, Simrol, Khandwa Road, Indore 453552, India.
ACS Omega. 2019 Aug 2;4(8):13153-13164. doi: 10.1021/acsomega.9b01201. eCollection 2019 Aug 20.
Development of nanozymes, which are nanomaterials with intrinsic enzymatic properties, has emerged as an appealing alternative to the natural enzymes with tremendous application potential from the chemical industry to biomedicine. The self-assembled growth of micrometer-sized oxide materials with controlled nonspherical shapes can be an important tool for enhancing activity as artificial enzymes, as the formation of these superstructures often results in high surface area with favorable impact on catalytic activity. Herein, the growth of rod-shaped FeO microstructures via a one-pot microwave-based method and using a water-poly(ethylene glycol) mixture as a solvent is reported, without the involvement of external shape-directing agents. The precursor metal salt played a key role in the size, shape, and phase selective evolution of iron oxide micro/nanomaterials. Whereas self-assembled microrod superstructures were obtained using Fe(NO) as the metal salt precursor, use of FeCl or Fe-acetate as precursors afforded hollow FeO microparticles and FeO nanoparticles, respectively. A graphitic layer was deposited on the FeO surface, imparting a negative surface charge as a result of a high-temperature treatment of poly(ethylene glycol). The rod-shaped FeO microcrystals show efficient peroxidase-mimicking activity toward 3,3,5,5'-tetramethylbenzidine and pyrogallol as peroxidase substrates with a Michaelis-Menten rate constant ( ) value of 0.05 and 0.52 mM, respectively. The proficient enzyme mimicking behavior of these magnetic superstructures was further explored for the degradation of organic dyes that includes rhodamine B, methylene blue, and methyl orange with a rate constant () of 0.038, 0.011, and 0.007 min respectively, using HO. This fast and simple method could help to develop a new pathway for differently shaped oxide nanoparticles in a sustainable and economical manner that can be harnessed as nanozymes for industrial as well as biological applications.
纳米酶是一类具有内在酶特性的纳米材料,其发展已成为天然酶颇具吸引力的替代物,在从化学工业到生物医学等领域具有巨大的应用潜力。具有可控非球形形状的微米级氧化物材料的自组装生长,可成为增强作为人工酶活性的重要工具,因为这些超结构的形成通常会产生高表面积,对催化活性产生有利影响。在此,报道了通过基于一锅法微波的方法并使用水 - 聚乙二醇混合物作为溶剂来生长棒状FeO微结构,且不涉及外部形状导向剂。前体金属盐在氧化铁微/纳米材料的尺寸、形状和相选择性演变中起关键作用。以Fe(NO)作为金属盐前体可获得自组装微棒超结构,而使用FeCl或醋酸铁作为前体分别得到空心FeO微粒和FeO纳米颗粒。通过对聚乙二醇进行高温处理,在FeO表面沉积了一层石墨层,赋予其负表面电荷。棒状FeO微晶对作为过氧化物酶底物的3,3,5,5'-四甲基联苯胺和邻苯三酚表现出高效的过氧化物酶模拟活性,米氏速率常数()值分别为0.05和0.52 mM。进一步探索了这些磁性超结构对包括罗丹明B、亚甲基蓝和甲基橙在内的有机染料的降解的熟练酶模拟行为,使用H₂O₂时的速率常数()分别为0.038、0.011和0.007 min⁻¹。这种快速且简单的方法有助于以可持续和经济的方式为不同形状的氧化物纳米颗粒开辟一条新途径,这些纳米颗粒可作为纳米酶用于工业和生物应用。