Insightful understanding of charge carrier transfer in 2D/2D heterojunction photocatalyst: Ni-Co layered double hydroxides deposited on ornamental g-C3N4 ultrathin nanosheet with boosted molecular oxygen activation

Molecular oxygen is a green and low-cost oxidant, which can be activated to produce reactive oxygen species by solar-light-driven photocatalysis. Here, Ni-Co LDH infused C, O co-doped g-C3N4 two-dimensional (2D) ultrathin nanosheet was prepared by a simple thermal polymerization coupling hydrothermal method. The molecular oxygen activation was estimated by the quantitative determination of center dot O2- and 3,3 ',5,5 '-tetramethylbenzidine (TMB) oxidation. 2D/2D heterojunction exhibits impressive photocatalytic performance. The arrestive activation efficiency is derived from the regulated energy band position, the broadened solar light absorption range, and the enhanced photoexcited electron transfer. Benefitting from these merits, the surface charge transfer efficiency of 2D/2D heterojunction is promoted to 51.3% from 14.3% (g-C3N4). The surface recombination rate constant is reduced to 0.0011 s-1 from 0.0042 s-1 (g-C3N4). The feasible photocatalytic mechanism for molecular oxygen activation is expounded based on experimental analysis.

Automated summary

A novel Ni-Co LDH infused C, O co-doped g-C3N4 2D ultrathin nanosheet was prepared with impressive photocatalytic performance, enhanced activation efficiency, and improved surface charge transfer efficiency compared to g-C3N4. The feasible photocatalytic mechanism for molecular oxygen activation was explained based on experimental analysis.