Single step additive manufacturing (3D printing) of electrocatalytic anodes and cathodes for efficient water splitting. Issue 1 (30th October 2019)

• Record Type: Journal Article
• Authors: Hughes, Jack P.; dos Santos, Pãmyla L.; Down, Michael P.; Foster, Christopher W.; Bonacin, Juliano A.; Keefe, Edmund M.; Rowley-Neale, Samuel J.; Banks, Craig E.
• Is Part Of: Sustainable energy & fuels. Volume 4:Issue 1(2020)
• Page Start: 302
• Page End: 311
• Publication Date: 2019-10-30
• Subjects: Renewable energy sources -- Periodicals; Fuel cells -- Periodicals; Electric batteries -- Periodicals; Electrochemistry -- Periodicals; 660.297
• DOI: 10.1039/c9se00679f
• Languages: English
• ISSNs: 2398-4902

Abstract

Abstract : 2D-MoSe2 and Pt/C containing additive manufactured electrodes, which exhibit electrocatalysis towards the hydrogen evolution and oxygen evolution reactions. Abstract : We enhance the current capability of additive manufacturing (AM)/(3D printing) to produce electronic devices by presenting a facile methodology for the production of electroconductive/electrocatalytic AM polylactic acid (PLA) filaments containing electrocatalytic materials; 2D-MoSe2 (M), electro-conductive carbon (C) and 20% Pt on carbon (Pt/C). The AM printed structures/electrodes (AMEs) produced using these filaments display bespoke electrochemical signals, in this case, efficient catalysis towards the major reactions that occur within a water electrolyser, namely the hydrogen evolution reaction (HER) on the cathode and the oxygen evolution reaction (OER) on the anode without the need for any post-production treatments. Various percentage mass incorporations, of the additives, into the PLA filaments were explored, with a 25% mass incorporation representing an ideal compromise between electroactivity and printability. Utilizing the optimized M10% –C15% -AME and Pt/C25% -AME as the cathode and anode, respectively, whilst a commercially available alkaline battery applied a potential of 1.5 V, water-splitting was achieved with obvious effervescence occurring at each electrode. This AM technique could mitigate the need for complex fabrication procedures, allowing researchers, industry and any interested individuals to rapidly go from 'desktop designs' to workable electrochemical prototype devices.