The glucose concentration in human blood can have a worrisome impact on human health, so the distribution of blood glucose contaminants in the human body is an important indicator that can be used to monitor diabetes. Diabetes affects many parts of the human body, such as neurological impairment, erectile dysfunction, and hardening of the arteries resulting in organ loss. In this study, cyclic voltammetry (CV) was used to process the electrical properties of a solution by preparing electrodes with CuO nanoparticles modified ZnO tetrapod nanostructures deposited on fluorine-doped tin oxide glass (CuO/ZnO/FTO). The measurements were processed in glucose solutions of different concentrations purposing for developing the sensitivity of the sensor. Different immersion times in the precursor copper sulfate solution were also used for preparing the electrode and carried out for electrochemical studies to adjust the electrode capability. The modified electrode, which was immersed in copper sulfate for 30 s, was efficient in detecting glucose molecules in different concentrations at the potential of +0.6 V. The rising slope is strongly and positively correlated with the concentration of glucose. One of the significant results is the indication that glucose concentration is linearly proportional to the current value of CV. After the measurement test with the addition of interference, the sensor can still identify the glucose concentration in the solution without being affected. This result proves that the sensor has considerable potential for developing into a high-performance non-enzymatic glucose sensor.

A variety of chemical sensing materials and procedures for conveniently detecting mercuric ion (II) (Hg2+) have been extensively explored. The detection challenges for accomplishing a simple, fast, and low investment procedure at the ultrasensitive level are ongoing. Herein we report a quadrillionth level for detecting Hg2+ by the surface-enhanced Raman scattering (SERS) technique. There is an interaction of silver nanoparticles decorated on a zinc-oxide tetrapod structure and coated on FTO glass (Ag@ZnO-FTO) with an organic ligand. 4,4′-Dipyridyl (DPy) performed as being chemisorbed by Ag nanoparticles interacting with a pyridine ring to produce plasmonic hot spots for SERS. The morphology of the surface and porous structure of the tetrapod becomes the powerful platform for enhanced SERS performance of DPy detection. In the absence of the augmentative electrolyte, the enhancement factor for DPy is more than 107. The inhibiting of the aggregation between Ag and DPy was present following the appearance of Hg2+, demonstrated by the quenching of the SERS signal from the DPy molecules. The capability to reproduce and the selectivity of the sensing by DPy were both demonstrated. In addition, the applications for detecting Hg2+ in natural water and beverages were successfully detected. These results demonstrated the SERS sensors had the potential for detecting Hg2+ in practical use.

Detecting pesticides using techniques that involve simple fabrication methods and conducting the detection at very low levels are challenging. Herein, we report the detection of acetamiprid at the quadrillionth level using surface-enhanced Raman scattering (SERS). The SERS chip comprises Ag nanoparticles deposited on a tetrapod structure of ZnO coated onto indium tin oxide glass (denoted as Ag@ZnO-ITO). Controlled Ag decoration of ZnO occurs via irradiation-induced synthesis. The morphology of the surface plays a significant role in achieving an enhanced SERS performance for acetamiprid detection. 4,4′-Dipyridyl (DPY) is used to investigate synthesis conditions for the chip, leading to an optimal irradiation time of 60 min. Furthermore, the enhancement factor for acetamiprid on Ag@ZnO-ITO is higher than 107. These results demonstrate that SERS sensors have the potential for practical use in acetamiprid detection.