• 文献标题:   Nitrogen-Doped Graphene-Encapsulated Nickel Cobalt Nitride as a Highly Sensitive and Selective Electrode for Glucose and Hydrogen Peroxide Sensing Applications
  • 文献类型:   Article
  • 作  者:   DEEPALAKSHMI T, TRAN DT, KIM NH, CHONG KT, LEE JH
  • 作者关键词:   sensor, glucose, hydrogen peroxide, nickel cobalt nitride, coreshell
  • 出版物名称:   ACS APPLIED MATERIALS INTERFACES
  • ISSN:   1944-8244
  • 通讯作者地址:   Chonbuk Natl Univ
  • 被引频次:   10
  • DOI:   10.1021/acsami.8b15069
  • 出版年:   2018

▎ 摘  要

To explore a natural nonenzymatic electrode catalyst for highly sensitive and selective molecular detection for targeting biomolecules is a very challenging task. Metal 2 nitrides have attracted huge interest as promising electrodes for glucose and hydrogen peroxide (H2O2) sensing applications due to their exceptional redox properties, superior electrical conductivity, and superb mechanical strength. However, the deprived electrochemical stability 600 Time (s) extremely limits the commercialization opportunities. Herein, novel nitrogen-doped graphene-encapsulated nickel cobalt nitride (NiCo3-xN/NG)core-shell nanostructures controllable molar ratio of Ni/Co are successfully fabricated and employed as highly sensitive and selective electrodes for glucose and H2O2 sensing applications. The highly sensitive and selective properties of the optimized core-shell NiCo2N/NG electrode are because of the high synergistic effect of the NiCo2N core and the NG shell, as evidenced by a superior glucose sensing performance with a short response time of <3 s, a wide linear range from 2.008 mu M to 7.15 mM, an excellent sensitivity of 1803 mu A mM(-1) cm(-2), and a low detection limit of 50 nM (S/N = 3). Furthermore, the core-shell NiCo2N/NG electrode shows excellent H2O2 sensing performances with a short response time of < 3 s, a wide detection range of 200 nM to 3.4985 mM, a high sensitivity of 2848.73 mu A mM(-1) cm(-2), and ultra-low limit detection of 200 nM (S/N = 3). The NiCo2N/NG sensor can also be employed for glucose and H2O2 detection in human blood serum, promising its application toward the determination of glucose and H2O2 in real samples.