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F. Silveri, F. D. Pelle, D. Rojas, D. Compagnone
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The resulting few-layers graphene flakes intercalated with CT aromatic skeleton ensure strict electrical contact among graphene sheets, whereas the fully reversible quinoid electrochemistry (ΔE = 28 mV, Ip, a/Ip, c = ⁓1) is attributed to the residual catechol moieties, which work as an electrochemical mediator. The GF-CT intimate electrochemistry is generated directly during the LPE of graphite, not requiring any modification or electro-polymerization steps, resulting in stable (8 months) and reproducible material. The electrocatalytic activity has been proven towards hydrazine (HY) and β-nicotinamide adenine dinucleotide (NADH), a pollutant and a coenzyme, respectively. High sensitivity in extended linear ranges (HY: LOD = 0.1 μM, L.R. 0.5–150 μM; NADH: LOD = 0.6 μM, L.R. 2.5–200 μM) at low overpotential (+0.15 V) was obtained using amperometry, avoiding electrode-fouling. 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引用次数: 0

摘要

植物化学产品开始被用来帮助二维纳米材料去角质。然而,对于所涉及的分子及其产生功能材料的能力缺乏研究是显而易见的。在这项工作中,提出了一种新的绿色液相脱落策略(LPE),其中类黄酮即儿茶素(CT)专门帮助导电水溶性石墨烯纳米片(GF)中的大块石墨脱落。物理化学和电化学方法被用来表征GF-CT的形态、结构和电化学特征。令人惊讶的是,所得的GF-CT整合了定义明确的电活性类醌加合物。由此产生的嵌入CT芳骨架的几层石墨烯片确保了石墨烯片之间的严格电接触,而完全可逆的醌类电化学(ΔE = 28 mV, Ip, a/Ip, c =⁓1)归因于残余的邻苯二酚部分,它作为电化学介质起作用。GF-CT亲密电化学是在石墨的LPE过程中直接产生的,不需要任何改性或电聚合步骤,从而产生稳定(8个月)和可再生的材料。对污染物肼(HY)和辅酶β-烟酰胺腺嘌呤二核苷酸(NADH)分别进行了电催化实验。在扩展线性范围内灵敏度高(HY: LOD = 0.1 μM, L.R. 0.5 ~ 150 μM;低过电位(+0.15 V)下NADH: LOD = 0.6 μM, lr为2.5 ~ 200 μM,避免了电极结垢。与石墨商业电极和用常规表面活性剂剥离的石墨烯相比,得到了更好的性能。GF-CT成功用于环境和生物基质中HY和NADH的检测(回收率94-107%,RSD≤8%),证明了该材料在具有挑战性的分析应用中的可开发性。在课程研究中,目标是将GF-CT的固有导电性与柔性衬底结合起来,构建能够容纳GF-CT专用导电膜的柔性电极/器件。在我们看来,本文提出的GF-CT是一种具有成本效益和可持续性的材料,在(生物)传感领域尤其具有吸引力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
P
Phytochemical products start to be employed to assist 2D nanomaterials exfoliation. However, a lack of studies regarding the molecules involved and their capacity to give rise to functional materials is evident. In this work, a novel green liquid-phase exfoliation strategy (LPE) is proposed wherein a flavonoid namely catechin (CT) exclusively assists the exfoliation of bulk graphite in conductive water-soluble graphene nanoflakes (GF). Physicochemical and electrochemical methods have been employed to characterize the morphological, structural, and electrochemical features of the GF-CT. Surprisingly, the obtained GF-CT integrates well-defined electroactive quinoid adducts. The resulting few-layers graphene flakes intercalated with CT aromatic skeleton ensure strict electrical contact among graphene sheets, whereas the fully reversible quinoid electrochemistry (ΔE = 28 mV, Ip, a/Ip, c = ⁓1) is attributed to the residual catechol moieties, which work as an electrochemical mediator. The GF-CT intimate electrochemistry is generated directly during the LPE of graphite, not requiring any modification or electro-polymerization steps, resulting in stable (8 months) and reproducible material. The electrocatalytic activity has been proven towards hydrazine (HY) and β-nicotinamide adenine dinucleotide (NADH), a pollutant and a coenzyme, respectively. High sensitivity in extended linear ranges (HY: LOD = 0.1 μM, L.R. 0.5–150 μM; NADH: LOD = 0.6 μM, L.R. 2.5–200 μM) at low overpotential (+0.15 V) was obtained using amperometry, avoiding electrode-fouling. Improved performances compared with graphite commercial electrodes and graphene exfoliated with a conventional surfactant, were obtained. The GF-CT was successfully used to perform the detection of HY and NADH (recoveries 94–107%, RSD ≤ 8%) in environmental and biological matrices, proving the material exploitability even in challenging analytical applications. On course studies, aim to combine the intrinsic conductivity of the GF-CT with flexible substrates, to construct flexible electrodes/devices able to housing GF-CT-exclusively composed conductive films. In our opinion, the here proposed GF-CT elects itself as a cost-effective and sustainable material, particularly captivating in the (bio)sensoristics scenario.
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