Electrocatalysts of the hydrogen evolution and oxidation reactions (HER and HOR) are of critical importance for the realization of future hydrogen economy. In order to make electrocatalysts economically competitive for large-scale applications, increasing attention has been devoted to developing noble metal-free HER and HOR electrocatalysts especially for alkaline electrolytes due to the promise of emerging hydroxide exchange membrane fuel cells. Herein, we report that interface engineering of Ni₃N and Ni results in a unique Ni₃N/Ni electrocatalyst which exhibits exceptional HER/HOR activities in aqueous electrolytes. A systematic electrochemical study was carried out to investigate the superior hydrogen electrochemistry catalyzed by Ni₃N/Ni, including nearly zero overpotential of catalytic onset, robust long-term durability, unity Faradaic efficiency, and excellent CO tolerance. Density functional theory computations were performed to aid the understanding of the electrochemical results and suggested that the real active sites are located at the interface between Ni₃N and Ni.

Transition metal phosphides (TMPs) have recently emerged as a new class of pre-catalysts that can efficiently catalyze the oxygen evolution reaction (OER). However, how the OER activity of TMPs varies with the catalyst composition has not been systematically explored. Here, we report the alkaline OER electrolysis of a series of nanoparticulate phosphides containing different equimolar metal (M = Fe, Co, Ni) components. Notable trends in OER activity are observed, following the order of FeP < NiP < CoP < FeNiP < FeCoP < CoNiP < FeCoNiP, which indicate that the introduction of a secondary metal(s) to a mono-metallic TMP substantially boosts the OER performance. We ascribe the promotional effect to the enhanced oxidizing power of bi- and tri-metallic TMPs that can facilitate the formation of MOH and chemical adsorption of OH⁻ groups, which are the rate-limiting steps for these catalysts according to our Tafel analysis. Remarkably, the tri-metallic FeCoNiP pre-catalyst exhibits exceptionally high apparent and intrinsic OER activities, requiring only 200 mV to deliver 10 mA cm⁻² and showing a high turnover frequency (TOF) of ≥0.94 s⁻¹ at the overpotential of 350 mV.

In this article, we for the first time report the synthesis and electrocatalytic properties of ruthenium cobalt phosphide hybrid clusters for the hydrogen evolution reaction (HER). Two types of catalysts are investigated: wet chemical reduction of Ru³⁺ on pre-formed cobalt phosphide (CoP) nanoparticles results in ruthenium–cobalt phosphide side-by-side structures (Ru/CoP); while phosphorizing chemically reduced RuCo alloy leads to the formation of hybrid ruthenium cobalt phosphide (RuCoP) clusters. Compared to pristine Ru clusters, both Ru/CoP and RuCoP show significantly improved HER performance in both acidic and alkaline solutions. In particular, the hybrid RuCoP clusters demonstrate a considerably low overpotential (η₁₀) of 11 mV at −10 mA cm⁻² and a high turnover frequency (TOF) of 10.95 s⁻¹ at η = 100 mV in 0.5 M H₂SO₄. Even in 1.0 M KOH the excellent HER activity of the RuCoP clusters remains, with a very low η₁₀ of 23 mV and exceptionally high TOF value of 7.26 s⁻¹ at η = 100 mV. Moreover, the RuCoP catalysts can sustain galvanostatic electrolysis in both acidic and alkaline solutions at −10 mA cm⁻² for 150 h with little degradation, showing better catalytic stability than the state-of-the-art commercial Pt/C catalysts. Our density functional theory (DFT) calculations indicate that the RuCoP hybrid exhibits a hydrogen adsorption energy very close to that of Pt and water and –OH adsorption energies distinct from pristine Ru, which reasonably explain the experimentally observed excellent HER activities and highlight the importance of synergistic coupling with cobalt phosphide to boost the HER performance of ruthenium.

The fundamentals, standardization, innovative strategies, and future direction of low-temperature water electrolysis including alkaline (AWE), proton exchange membrane (PEMWE), and anion exchange membrane (AEMWE) water electrolyses are discussed.

Dynamic morphological, structural and compositional changes will occur when transition metal phosphides and chalcogenides are used to catalyze the oxygen evolution reaction, which can substantially enhance their electrocatalytic performance.