化学
抗坏血酸
异质结
光电流
氮化碳
生物传感器
选择性
半导体
分析物
光电化学
石墨氮化碳
纳米技术
电解质
光电子学
电极
光催化
材料科学
催化作用
电化学
生物化学
色谱法
食品科学
物理化学
作者
Wang Li,Mingming Zhang,Dan Han,Hong Yang,Qing Hong,Yanfeng Fang,Zhixin Zhou,Yanfei Shen,Songqin Liu,Chaofeng Huang,Hai‐Bin Zhu,Yuanjian Zhang
出处
期刊:Analytical Chemistry
[American Chemical Society]
日期:2023-08-31
卷期号:95 (36): 13716-13724
被引量:19
标识
DOI:10.1021/acs.analchem.3c03221
摘要
Photoelectrochemical (PEC) sensing enables the rapid, accurate, and highly sensitive detection of biologically important chemicals. However, achieving high selectivity without external biological elements remains a challenge because the PEC reactions inherently have poor selectivity. Herein, we report a strategy to address this problem by regulating the charge-transfer pathways using polymeric carbon nitride (pCN)-based heterojunction photoelectrodes. Interestingly, because of redox reactions at different semiconductor/electrolyte interfaces with specific charge-transfer pathways, each analyte demonstrated a unique combination of photocurrent-change polarity. Based on this principle, a pCN-based PEC sensor for the highly selective sensing of ascorbic acid in serum against typical interferences, such as dopamine, glutathione, epinephrine, and citric acid was successfully developed. This study sheds light on a general PEC sensing strategy with high selectivity without biorecognition units by engineering charge-transfer pathways in heterojunctions on photoelectrodes.
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