A novel design of urea-assisted hydrogen production in electrochemical–chemical decoupled self-circulating systems

Abstract

In traditional water electrolysis processes, the oxidation and reduction reactions of water are coupled in both time and space, which presents significant challenges. Here, we propose an optimized design for an electrochemical–chemical self-circulating decoupled system. This system uses the continuous Ni²⁺/Ni³⁺ redox process on nickel hydroxide electrode sheets to stepwise couple the urea oxidation-assisted hydrogen production system, separating the hydrogen evolution reaction (HER) and urea oxidation reaction (UOR) into two distinct steps: electrochemical and chemical reactions. In the first electrochemical step, water is reduced at the cathode to produce hydrogen, while the single-electron electrochemical oxidation of Ni(OH)₂ at the anode generates NiOOH. Then, in the second chemical reaction step, NiOOH spontaneously oxidizes urea, causing its decomposition and simultaneously reducing back to the Ni(OH)₂ state. We concurrently investigated the effects of temperature and OH-concentration on the spontaneous oxidation of urea. At 80 °C and with a 1 M KOH concentration containing 50 mg of urea solution, the NiOOH electrode successfully catalyzed the spontaneous decomposition of urea, achieving conversion rate of 100% and faradaic efficiency of 98%.