石墨烯
生物传感器
纳米技术
材料科学
场效应晶体管
晶体管
共价键
吸附
生物污染
二价
纳米传感器
蛋白质吸附
选择性
单体
阳离子聚合
跨导
聚合物
金属有机骨架
作者
Bing Sun,Qi Shu,Lang Wang,Kaicong Liu,Teng Gao
出处
期刊:Nano Letters
[American Chemical Society]
日期:2025-10-06
卷期号:25 (41): 15150-15157
被引量:4
标识
DOI:10.1021/acs.nanolett.5c04572
摘要
Graphene field-effect transistors (GFETs) promise label-free biosensing but suffer from nonspecific protein adsorption and poor selectivity in complex biofluids. Herein, we proposed a surface-engineering strategy to endow GFET arrays with antifouling robustness and molecular-sieving selectivity. Two fluorine-rich covalent organic framework (F-COF) films synthesized at the liquid-liquid interface were transferred onto GFET channels through a gentle, solvent-free lamination protocol, creating F-COF/GFET sensors with high transconductance and typical bipolar characteristics of graphene. F-COF films in the modified GFET sensors functioned as size-selective gates for smaller metal ions (e.g., divalent cations like Zn2+), but excluded anionic methyl orange and larger cationic Rhodamine B. The F-COF/GFET sensors reduced the nonspecific protein adsorption and allowed the detection of Ca2+ at low concentrations (10-6 M) when exposed to a simulated physiological milieu containing 10-4 M bovine serum albumin. Decoupling antifouling from recognition at the monomer level provides a generalizable strategy for selective, real-time GFET biosensors in biofluids.
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