电化学发光
计时安培法
材料科学
胶体金
电极
电化学
循环伏安法
分析化学(期刊)
工作电极
扫描电子显微镜
玻璃碳
纳米颗粒
纳米技术
化学
色谱法
复合材料
物理化学
作者
Nurul Izzati Akmal Mohd Azman,Nur Syakimah Ismail,Nur Hamidah Abdul Halim,Nurjuliana Juhari,Norhayati Sabani,Toibah Abd Rahim,Siti Aisyah Shamsudin,Eiichi Tamiya
标识
DOI:10.58915/ijneam.v16idecember.399
摘要
In this work, the electrodeposition method was utilized to form gold nanoparticles on a carbon screen-printed electrode (SPE) using chronoamperometry at -0.4 V with various durations from 50 to 200 seconds. Scanning Electron Microscopy (SEM) images have proven that the electrodeposition method is capable of uniformly forming AuNPs on SPE (AuNPs- SPE). Apart from that, electrodeposition durations have increased the size of AuNPs by up to 66% based on average size measurements using ImageJ software. It can be observed that long electrodeposition durations permit the agglomeration of AuNPs on the electrode surface. The effect of electrodeposition duration on electrocatalytic performance in potassium ferricyanide and electrochemiluminescence (ECL) intensity of nitrogen-doped carbon dots (NCDs) was evaluated. Cyclic voltammetry (CV) of ferricyanide demonstrates that as the electrodeposition duration increases, AuNPs-SPE shows better electrochemical performance than bare SPE. ECL of NCDs displays that 100 s electrodeposition durations give the highest ECL intensity of 184% compared to bare SPE and have been chosen as the optimum parameter. The ECL mechanisms of bare SPE and AuNPs-SPE reveal that AuNPs- SPE has greater electrochemical and ECL performance than bare SPE, as evidenced by the CV of AuNPs-SPE having a faster reduction current, which rises to 87.2% ECL intensity and 510 mV faster ECL occurrence. These phenomena confirmed that the electrodeposition of AuNPs has improved the conductivity of SPE.
科研通智能强力驱动
Strongly Powered by AbleSci AI