Non-noble metal (Ni, Cu)-carbon composite derived from porous organic polymers for high-performance seawater electrolysis

The hydrothermal preparation of o-dianisidine and triazine interlinked porous organic polymer and its successive derivatisation via metal infusion (Ni, Cu) under hydrothermal and calcination conditions (700 degrees C) to yield pristine (ANIPOP-700) and Ni/Cu decorated porous carbon are described here (Ni-ANIPOP-700 and Cu-ANIPOP-700). To confirm their chemical and morphological properties, the as-prepared materials were methodically analyzed using solid state C-13 and N-15 NMR, X-ray diffraction, Raman spectroscopy, field emission scanning and high resolution transmission electron microscopic techniques, and x-ray photoelectron spectroscopy. Furthermore, the electrocatalytic activities of these electrocatalysts were thoroughly investigated under standard oxygen evolution (OER) and hydrogen evolution reaction (HER) conditions. The results show that all of the materials demonstrated significant activity in water splitting as well as displayed excellent stability (22 h) in both acidic (HER) and basic conditions (OER). Among the electrocatalysts reported in this study, Ni-ANIPOP-700 exhibited a lower overpotential eta(10) of 300 mV in basic medium (OER) and 150 mV in acidic medium (HER), as well as a lower Tafel slope of 69 mV/dec (OER) and 181 mV/dec (HER), indicating 30% lower energy requirement for overall water splitting. Gas chromatography was used to examine the electrolyzed products.

Automated summary

In this study, a hydrothermal method was used to prepare a porous organic polymer, which was subsequently derivatised with metal infusion under high temperature and calcination conditions to obtain pristine and metal-decorated porous carbons. These electrocatalysts showed significant activity in water splitting and excellent stability, with Ni-ANIPOP-700 exhibiting lower overpotential and Tafel slope, indicating lower energy requirements for overall water splitting. Gas chromatography was used to analyze the electrolyzed products.