Faculty of Industrial Sciences and Technology, Universiti Malaysia Pahang, Kuantan 26300, Malaysia.
Department of Chemistry and Biochemistry, Kent State University, Kent, OH 44242, USA.
Biosensors (Basel). 2023 Jun 22;13(7):671. doi: 10.3390/bios13070671.
An amperometric enzyme-free hydrogen peroxide (HO) sensor was developed by catalytically stabilizing active gold nanoparticles (Au NPs) of 4-5 nm on a porous titanium dioxide nanotube (TiO NTs) electrode. The Au NPs were homogeneously distributed on anatase TiO NTs with an outer diameter of ~102 nm, an inner diameter of ~60 nm, and a wall of thickness of ~40 nm. The cyclic voltammogram of the composite electrode showed a pair of redox peaks characterizing the electrocatalytic reduction of HO. The entrapping of Au NPs on TiO NTs prevented aggregation and facilitated good electrical conductivity and electron transfer rate, thus generating a wide linear range, a low detection limit of ~104 nM, and high sensitivity of ~519 µA/mM, as well as excellent selectivity, reproducibility, repeatability, and stability over 60 days. Furthermore, excellent recovery and relative standard deviation (RSD) were achieved in real samples, which were tap water, milk, and bacteria, thereby verifying the accuracy and potentiality of the developed nonenzymatic sensor.
一种安培无酶过氧化氢(HO)传感器通过在多孔二氧化钛纳米管(TiO NTs)电极上催化稳定 4-5nm 的活性金纳米颗粒(Au NPs)来开发。Au NPs 在锐钛矿 TiO NTs 上均匀分布,其外径约为 102nm,内径约为 60nm,壁厚约为 40nm。复合电极的循环伏安图显示了一对特征性的氧化还原峰,表明 HO 的电催化还原。Au NPs 在 TiO NTs 上的包埋防止了聚集,并促进了良好的导电性和电子转移率,从而产生了宽的线性范围、低检测限约为 104nM 和高灵敏度约为 519µA/mM,以及出色的选择性、重现性、重复性和 60 天以上的稳定性。此外,在实际样品(如自来水、牛奶和细菌)中实现了优异的回收率和相对标准偏差(RSD),从而验证了所开发的非酶传感器的准确性和潜力。