化学
胆碱氧化酶
异质结
跨导
检出限
金属有机骨架
晶体管
光电子学
纳米技术
光电化学
色谱法
有机化学
电化学
电极
吸附
物理化学
电压
物理
酶
量子力学
材料科学
乙酰胆碱酯酶
作者
Xiaomei Shi,Zhen Wang,M. Chen,Qingqing Wu,Feng‐Zao Chen,Gao‐Chao Fan,Weiwei Zhao
标识
DOI:10.1021/acs.analchem.4c00173
摘要
Recently, organic photoelectrochemical transistor (OPECT) bioanalysis has become a prominent technique for the high-performance detection of biomolecules. However, as a sensitive index of the OPECT, the dynamic regulation transconductance (gm) is still severely deficient. Herein, this work reports a new photosensitive metal–organic framework (MOF-on-MOF) heterostructure for the effective modulation of maximum gm and natural bienzyme interfacing toward choline detection. Specifically, the bidentate ligand MOF (b-MOF) was assembled onto the UiO-66 MOF (u-MOF) by a modular assembly method, which could facilitate the charge separation and generate enhanced photocurrents and offer a biophilic environment for the immobilization of choline oxidase (ChOx) and horseradish peroxidase (HRP) through hydrogen-bonded bridges. The transconductance of the OPECT could be flexibly altered by increased light intensity to maximal value at zero gate bias, and sensitive choline detection was achieved with a detection limit of 0.2 μM. This work reveals the potential of MOF-on-MOF heterostructures for futuristic optobioelectronics.
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