Self-assembly of functionalized Echinops-like Rh porous nanostructure electrocatalysts for highly efficient seawater splitting

Although water electrolysis provides a promising technology for global hydrogen economics, highly efficient electrocatalysts are required to boost the sluggish kinetics of both hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) under neutral conditions. Herein, we synthesized novel polyethyleneimine (PEI) functionalized Echinops-like Rh porous nanostructures (Echinops-like Rh PNNSs) by a solvothermal method, which originated from the self-assembly of Rh two-dimensional (2D) sub-nanoflakes with 1.2 nm thickness. As a good electron donor, -NH2 on PEI could modulate the electronic structure of Echinops-like Rh PNNSs, reducing the adsorption energy of H2O on the surface of Echinops-like Rh PNNSs. Meanwhile, -NH2 groups could specifically enrich H2O molecules under neutral conditions, which facilitates water splitting. The as-synthesized Echinops-like Rh PNNSs exhibit high HER activity with ultralow overpotential, low Tafel slope, and excellent stability. Moreover, the Echinops-like Rh PNNSs also showed an enhanced OER activity than commercial RuO2 with a small overpotential of 79.5 mV at 10 mA cm(-2) in neutral media. When using Echinops-like Rh PNNSs as both anode and cathode catalysts for overall seawater splitting, a cell voltage of only 1.61 V is needed for generating 10 mA cm(-2) current density, greatly boosting the efficiency of seawater splitting.

Automated summary

This study successfully synthesized novel polyethyleneimine (PEI) functionalized Echinops-like Rh porous nanostructures with high efficiency in both hydrogen and oxygen evolution reactions under neutral conditions. The structures exhibited excellent stability and enhanced activity compared to commercial catalysts, showing potential for improving the efficiency of seawater splitting.