Aerophobic P-MoS₂ on MOF-Derived Co,N-Codoped Carbon Nanosheets with Accelerated H₂ Bubble Release Dynamics for...

Rapid bubble release at high current densities results in the detachment of catalysts and performance degradation, posing a persistent challenge in actual alkaline water electrolysis (AWE). Here, hierarchical nanosheet structures (CoNC@P-MoS₂) are constructed, with P-doped MoS₂ on the surface of Co,N-codoped carbon. It exhibits low hydrogen evolution reaction overpotentials of 30 and 354 mV at 10 and 1000 mA cm^-2 in 1 M KOH, respectively, with a small Tafel slope of 36 mV dec^-1. The constructed CoNC@P-MoS₂||NiFe-DLH cell requires only 1.44 and 1.92 V to achieve overall water splitting at 10 and 1000 mA cm^-2, which outperforms the traditional catalysts like Pt/C||IrO₂. The introduction of P stabilizes surface hydroxyl (OH*) and increases the proton penetration depth, thereby greatly enhancing its intrinsic activity. It also makes the surface aerophobic by introducing more microfeatures, which greatly improves the geometric activity by increasing the bubble release rate (∼5.8 times). Low energy consumption of 3.92 kW h Nm^-3 was achieved with an energy efficiency close to 80%. Bubble growth kinetics analysis reveals that the time and growth factors for CoNC@P-MoS₂ are increased to 0.54 and 11.79 from 0.45 and 6.09 for CoNC, respectively, which highlights its fast bubble reaction dynamics. The results suggest the feasibility of CoNC@P-MoS₂ as a potential high-performance catalyst in commercial AWE.