Energy-efficient hydrogen production coupled with methanol oxidation using NiFe LDH@NiMo alloy heterostructure

The traditional electrochemical water splitting is extremely restricted by the sluggish kinetics of the anodic oxygen evolution reaction (OER). In this context, replacing OER with a more thermodynamic favorable oxidation reaction, such as methanol oxidation reaction (MOR), is an effective strategy to improve the hydrogen evolution reaction (HER) efficiency while still obtaining some valuable by-products. In this work, nickel-iron layered double-hydroxide [NiFe LDH]@NiMo alloy heterostructure is synthesized by electrodeposition process and its bi-functional electrocatalytic activities for both hydrogen evolution reaction (HER) and methanol oxidation reaction (MOR) are evaluated. For the HER, the catalyst exhibits low overpotential of 82.5 mV at 100 mA/cm2, with a Tafel slope of 61 mV/dec as well as splendid long-term stability. For the MOR, the required potential decreases by 74 mV at 100 mA/cm2 compared to oxygen evolution reaction (OER). Moreover, 97% process yields toward value-added formic acid (HCOOH) are obtained at the anode, with a faradaic efficiency of approximately 100% for HER at the cathode. The superior catalytic performance results from the synergic contribution of NiFe LDH and NiMo alloy. The formation of NiFe LDH@NiMo alloy heterostructure leads to the redistribution of electrons among nickel (Ni), iron (Fe) and molybdenum (Mo) elements. Therefore, the charge transfer process has been greatly promoted. This study provides a scalable energy saving strategy for hydrogen energy development.