电催化剂
电化学
葡萄糖氧化酶
催化作用
生物传感器
过氧化氢
纳米技术
电子转移
微透析
体内
材料科学
化学
电极
组合化学
光化学
有机化学
生物化学
细胞外
生物
物理化学
生物技术
作者
Hanfeng Hou,Junjie Mao,Yunhu Han,Fei Wu,Meining Zhang,Dingsheng Wang,Lanqun Mao,Yadong Li
标识
DOI:10.1007/s11426-019-9605-0
摘要
Modulation of interfacial electron transfer has been proven to pave a new approach to in vivo electrochemical monitoring of brain chemistry; however, designing and establishing highly efficient electrocatalytic scheme towards neurochemicals remain a long-standing challenge. Here, we find that recently established single-atom catalyst (SAC) can be used for catalyzing the electrochemical process of physiologically relevant chemicals and thus offers a new avenue to in vivo electrochemical biosensing. To prove this new concept, we used Co single-atom catalyst (Co-SAC), in which the atomic active sites are dispersed in ordered porous N-doping carbon matrix at atomic level, as an example of SACs for analyzing glucose as the physiologically relevant model chemicals. We found that Co-SAC catalyzes the electrochemical oxidation of hydrogen peroxide (H2O2) at a low potential of ca. +0.05 V (vs. Ag/AgCl). This property was further used for developing an oxidase-based glucose biosensor that was used subsequently as a selective detector of an online electrochemical system (OECS) for continuous monitoring of microdialysate glucose in rat brain. The OECS with Co-SAC-based glucose biosensor as the online detector was well responsive to glucose without interference from other electroactive species in brain microdialysate. This study essentially offers a new approach to in vivo electrochemical analysis with SACs as electrocatalysts to modulate interfacial electron transfer.
科研通智能强力驱动
Strongly Powered by AbleSci AI