Abstract

Three-dimensional (3D) porous MXene-based aerogel architectures have attracted great interest for many applications, despite limits in renewable energy conversion owing to the lack of multifunctionality in their components. Herein, a simple and general strategy for constructing a novel functional 3D MXene-based composite heterojunction aerogel (MS@S-MAs) is presented via divalent metal-ion assembly and subsequent thermal sulfidation, and its application in electrochemical nitrogen reduction reaction (NRR) is studied. The as-prepared MS@S-MAs comprises metal sulfide nanoparticles uniformly confined in 3D interconnected conductive S-doped MXene sheets with intimate interfacial interaction. Benefiting from the unique properties and an interfacial interaction, MS@S-MAs exhibit significantly improved NRR catalytic performance and excellent stability because of the higher exposure of electrochemically active sites coupled with easier accessibility, faster mass diffusion, and quicker carrier transport at the interface. Remarkably, CoS@S-MAs show an NH3 yield rate and a Faradaic efficiency of 12.4 µg h-1 mg-1 cat and 27.05% at the lower potential of -0.15V versus a reversible hydrogen electrode in 0.1 m Na2 SO4 solution under ambient conditions, which rivals or exceeds most of the previously reported MXene-based and Co-based catalysts. This work will open avenues to construct 3D MXene-based materials with rich functionalities for energy storage and conversion, catalysis, and other applications.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

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.