Abstract
Rational design of electrocatalysts with the tuneable structural and electrocatalytic properties are essential to accomplish bifunctional activity of hydrogen and oxygen evolution reaction (HER/OER), and thus efficient water splitting systems. Here, we present a bifunctional hybrid electrocatalyst consisting of Co9S8 (OER-active) and MoS2 (HER-active) with the structural merits of hierarchical morphology, huge electrochemically active sites, and greater charge transfer ability. The structural features of the hybrid electrocatalyst (Co9S8@MoS2/N-doped hollow carbon) that is derived from metal organic framework (MOF) precursor are elaborately controlled by the temperature dependent-Kirkendall diffusion effect. Specifically, the imbalanced diffusion rates between two ionic species (Co2+ and S2−), confined in the MOF-precursor geometry, induces the formation of internal voids and outward growth of Co9S8 while retaining MoS2 layers on the surface. As a result, the hybrid electrocatalyst exhibits greatly enhanced HER (126 mV@−10 mA cm−2) and OER (233 mV@10 mA cm−2) performance. Furthermore, the bifunctional electrode couple demonstrates efficient overall water splitting performance (1.56 V@10 mA cm−2) compared to the benchmark electrode couple of IrO2/C//Pt/C (1.63 V@10 mA cm−2) in 1 M KOH solution. The results highlight that inducing “Kirkendall effect” through temperature-tuning approach for structure-properties modulation can be extensively applied to design various bifunctional hybrid electrocatalysts.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.