Graphene frameworks-confined synthesis of 2D-layered NiCoP for the electrochemical sensing of H2O2 at lower overpotential.

A new 2D-layered nickel cobalt phosphide nanosheet confined by 3D graphene frameworks (denoted as NiCoP/GFs) is in situ controllably synthesized as a highly efficient and durable electrocatalyst, which is obtained from the transformation of corresponding NiCo layer double hydroxides and GFs. Hydrogen peroxide (H2O2) is selected as a demonstration to study the electrochemical sensing performance of the NiCoP/GFs. Benefiting from 2D morphology of NiCoP and network structure of GFs, NiCoP/GFs exhibits remarkable electroactivity toward H2O2 at a relatively low overpotential of approximately - 0.3 V (vs sat. Ag/AgCl) in 0.01 M phosphate-buffered saline solution (PBS, pH = 7.4). The NiCoP/GFs-based H2O2 electrochemical sensor achieves a high sensitivity of ∼4398 μA mM-1 cm-2, a low detection limit of 0.028 ± 0.006 μM, and desirable selectivity. In addition, the sensor can sensitively detect H2O2 from living cancer cells. This study not merely broadens the synthesis methods of transition metal phosphide-based nanocrystals but the NiCoP/GFs also has broad prospects in diverse electrochemistry fields. We have reported a controllable synthesis of 2D nickel cobalt phosphide nanosheet confined by graphene frameworks (denoted as NiCoP/GFs) as a greatly efficient and durable electrocatalyst. The NiCoP/GFs exhibits remarkable electroactivity toward detection of H2O2 at a relatively low overpotential of approximately -0.3 V. Density functional theory (DFT) calculations further prove that regulation of the electronic structure of NiCoP by GFs lowers the adsorption free energy of *OOH intermediates, and thus contributes to the greatly improved the electrocatalytic performance of NiCoP/GFs toward H2O2 reduction. The developed NiCoP/GFs can be applied as excellent electrode materials for efficient electrochemical sensing of H2O2.