Wu Yuming, Idros Mohamed Nazmi, Feng Desheng, Huang Wengang, Burdyny Thomas, Wang Bo, Wang Geoff, Li Mengran, Rufford Thomas E
School of Chemical Engineering, The University of Queensland, St Lucia, Brisbane, Queensland 4072, Australia.
Materials for Energy Conversion and Storage (MECS), Department of Chemical Engineering, Faculty of Applied Sciences, Delft University of Technology, van der Maasweg 9, Delft 2629 HZ, The Netherlands.
ACS Appl Mater Interfaces. 2024 Oct 23;16(42):56967-56974. doi: 10.1021/acsami.4c09095. Epub 2024 Oct 11.
Electrolyte flooding in porous catalyst layers on gas diffusion electrodes (GDE) limits the stability and high-current performance of CO and CO electrolyzers. Here, we demonstrate the in situ electroreduction of graphene oxide (GO) to reduced graphene oxide (r-GO) within a silver catalyst layer on a carbon GDE. The r-GO introduces hydrophobicity regions in the catalyst layer that help mitigate electrolyte flooding during high current density CO electrolysis to CO. The flooding-resistant r-GO/Ag-coated GDE achieves a sustained Faradaic efficiency of CO at 94% for more than 8 h, compared to a rapid drop from 95% to 66% in an Ag-coated GDE without r-GO at 100 mA·cm. We found that GO enhances the electrochemically active surface area of the catalyst layer during CO electrolysis tests because the incorporation of GO increases the roughness of the catalyst layer. The in situ method of electrochemically reducing GO to r-GO provides a low-cost, practical approach that can be applied during standard spray-deposition procedures to develop flooding-resistant GDEs.
气体扩散电极(GDE)上多孔催化剂层中的电解质溢流限制了CO和CO电解槽的稳定性和高电流性能。在此,我们展示了在碳GDE上的银催化剂层内将氧化石墨烯(GO)原位电还原为还原氧化石墨烯(r-GO)。r-GO在催化剂层中引入了疏水区,有助于减轻在高电流密度下将CO电解为CO过程中的电解质溢流。与在100 mA·cm下没有r-GO的银涂层GDE中从95%迅速降至66%相比,具有抗溢流r-GO/Ag涂层的GDE在94%的CO法拉第效率下持续超过8小时。我们发现,在CO电解测试中,GO提高了催化剂层的电化学活性表面积,因为GO的掺入增加了催化剂层的粗糙度。将GO电化学还原为r-GO的原位方法提供了一种低成本、实用的方法,可在标准喷雾沉积过程中应用,以开发抗溢流GDE。