非阻塞I/O
材料科学
双金属片
葡萄糖氧化酶
电化学
化学工程
阳极
金属有机骨架
金属
吸附
纳米技术
生物传感器
催化作用
化学
电极
有机化学
冶金
物理化学
工程类
作者
A. Vignesh,Ponniah Vajeeston,Mehboobali Pannipara,Abdullah G. Al‐Sehemi,Yang Xia,G. Gnana kumar
标识
DOI:10.1016/j.cej.2021.133157
摘要
The hierarchical hollow architectured NiO/Co3O4/C is developed using the sacrificial template of Ni-Co MOF and the proximity of Ni(II)/Co(II) ions with organic ligand in Ni-Co MOF accelerates the generation of tightly pinned NiO/Co3O4 nanostructures with carbon. The elevated charge-transfer process among the constituents of as-formulated nanocatalysts and their structural and electronic relationship are established with DFT studies. The hollow architecture of NiO/Co3O4/C exposes both the inner and outer surfaces for an effectual glucose utilization, whilst the carbon interlaced metal nanoparticles and binary metal oxide synergism enumerate, respectively, the continual electron mobility and catalytically active channels, accelerating NiO/Co3O4/C loaded Biodegradable corn starch bag’s (BCSB) enzyme-free glucose sensing performance in human serum with high sensitivity and selectivity. The consistent flexible glucose electrooxidation acquired for NiO/Co3O4/C/BCSB under variant bending angles along with other unique concerts establish the bendable, binder-less, stable, reusable, and eco-friendly electrochemical probes for the evolution of revolutionary electrochemical diagnosis devices.
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