Unravelling the Photoelectrochemical Water Splitting of Nanometer‐Thick Carbon Nitride Layer

Abstract

AbstractMatching the thickness of the graphitic carbon nitride (CN) nanolayer with the charge diffusion length is expected to compensate for the poor intrinsic conductivity and charge recombination in CN for photoelectrochemical cells (PEC). Herein, the compact CN nanolayer with tunable thickness is in situ coated on carbon fibers. The compact packing along with good contact with the substrate improves the electron transport and alleviates the charge recombination. The PEC investigation shows CN nanolayer of 93 nm‐thick yields an optimum photocurrent of 116 µA cm−2 at 1.23 V versus RHE, comparable to most micrometer‐thick CN layers, with a low onset potential of 0.2 V in 1 m KOH under 1 sun illumination. This optimum performance suggests the electron diffusion length matches with the thickness of the CN nanolayer. Further deposition of NiFe‐layered double hydroxide enhanced the surface water oxidation kinetics, delivering an improved photocurrent of 210 µA cm−2 with IPCE of 12.8% at 400 nm. The CN nanolayer also shows extended potential in PEC organic synthesis. This work experimentally reveals the PEC behavior of the nanometer‐thick CN layer, providing new insights into CN in the application of energy and environment‐related fields.