纳米片
材料科学
光电化学
光电阴极
纳米颗粒
表面等离子共振
纳米技术
光电流
电解质
石墨烯
胶体金
生物传感器
氧化铟锡
光电子学
电化学
化学
图层(电子)
电子
电极
物理化学
物理
量子力学
作者
Jianyu Qiao,Yuhuan Wang,Shaohua Dong,Qing Liang,Shijun Shao
出处
期刊:ACS applied nano materials
[American Chemical Society]
日期:2023-03-20
卷期号:6 (7): 5664-5674
被引量:7
标识
DOI:10.1021/acsanm.3c00111
摘要
Photocathode-based photoelectrochemical (PEC) sensors can well evade the intrinsic hole oxidation reactions occurring at the photoelectrode–electrolyte interface and expand the application of PEC sensors in the field of bioanalysis. Herein, a cathodic PEC sensor based on p-type semiconductor bismuth oxyiodide nanosheet arrays (BiOI NSAs) integrated with gold nanoparticles (AuNPs) on indium-doped tin oxide (ITO) electrode (ITO/BiOI NSAs/AuNPs) is fabricated by a two-step electrodeposition method. The local surface plasmon resonance (LSPR) effect of AuNPs facilitates the capability of visible light absorption of the BiOI NSAs. Meanwhile, AuNPs, as an electron reservoir, improve the charge separation efficiency of carriers by forming a Schottky barrier, allowing more electrons to be transferred to O2 dissolved in the electrolyte, consequently promoting the PEC activity of the photoactive materials. Furthermore, dopamine (DA) can enhance the photocurrent of the ITO/BiOI NSAs/AuNPs photoelectrode by binding to Bi3+ on the BiOI NSAs surface to in-situ-form a charge-transfer complex (CTC). Based on this phenomenon, a PEC sensor was designed for the determination of DA, and the PEC sensor showed acceptable results for DA detection in real samples. The PEC sensor demonstrates the prospect of BiOI-based materials in cathodic PEC biosensing.
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