MOF-Derived Co3S4 Nanoparticles Embedded in Nitrogen-Doped Carbon for Electrochemical Oxygen Production

The development of a simple and effective strategy for designing a highly efficient oxygen evolution electrocatalyst is more important to speed up the efficiency-limiting step involved in water electrolysis. The high efficiency of the oxygen evolution reaction (OER) is directly correlated with the class of electrode materials employed. This work reports a series of Co3S4 nanoparticles (Co3S4-2h, Co3S4-3h, and Co3S4-4h) derived from a metal-organic framework (MOF) via a single-step annealing strategy with varying reaction times for the study of OER. During the annealing process, the MOF precursor [Co3(tiron-bpy)2(bpy)(H2O)8]center dot (H2O)2 termed as Co-T-BPY directly converted to cobalt sulfide (Co3S4) nanoparticles, along with additional support of the N-doped carbon moiety. Interestingly, variation of reaction time in a fixed temperature condition played a decisive role in optimizing the surface area with huge active sites of the derived products. The optimized Co3S4-3h product needed an overpotential of 285 mV to reach 10 mA cm-2 current density and an acceptable Tafel value (109 mV dec-1) with excellent 14 h of stability performance under harsh alkaline conditions. The OER results are attributed to the combined effect of the Co3S4 phase and N-doped carbon matrix, resulting in substantial stability and high conductivity. Therefore, we believe that the time variation strategy for the preparation of a cobalt-based non-precious electrode material can pave the way in search of an OER-efficient electrocatalyst.

Automated summary

The development of a simple and effective strategy for designing a highly efficient oxygen evolution electrocatalyst is crucial for improving the efficiency of water electrolysis. This study focuses on the synthesis of Co3S4 nanoparticles derived from a metal-organic framework using a single-step annealing strategy with varying reaction times. The optimized Co3S4-3h product exhibited excellent oxygen evolution reaction (OER) performance and stability under harsh alkaline conditions, attributed to the combination of the Co3S4 phase and N-doped carbon matrix. This research contributes to the search for non-precious electrode materials for efficient OER.