Bullmann Matheus, Suárez Andrés Cuña, Pacheco Sampaio Edna Jerusa, Pastorino Natalia Prieto, Hubler Roberto, Chinarro Eva, de Fraga Malfatti Célia
Corrosion Research Laboratory (LAPEC), Engineering School, Federal University of Rio Grande do Sul (UFRGS), Av. Bento Gonçalves, 9500, 91501-970 Porto Alegre, Rio Grande do Sul, Brazil.
Physical Chemistry Area, DETEMA, Faculty of Chemistry, University of the Republic (UDELAR), CC 1157, 11800 Montevideo, Uruguay.
ACS Omega. 2025 May 29;10(22):23297-23307. doi: 10.1021/acsomega.5c01734. eCollection 2025 Jun 10.
The production of green hydrogen via water electrolysis faces challenges due to the sluggish oxygen evolution reaction at the anode. In this study, we developed a self-supported bifunctional Pt/SnO/NbO/Nb electrocatalyst capable of coupling the hydrogen evolution reaction to the selective ethanol oxidation reaction (EOR) in an acidic medium. The catalyst demonstrated efficacy for the EOR, with an of +130 mV versus SHE results in a peak current density of 8.97 mA cm. The bifunctional electrocatalyst exhibited a spontaneous and rapid increase in current for the HER, achieving an overpotential of -48 mV for a current density of 5 mA cm and a Faradaic efficiency of 99.7%. This efficient coupling of the EOR with the HER reduces energy consumption for green hydrogen generation compared to traditional water splitting. With hydrogen being the sole gaseous product, the HER-EOR electrolysis system can operate effectively without a membrane, promising a more cost-effective, sustainable, and efficient green hydrogen production.
由于阳极析氧反应缓慢,通过水电解生产绿色氢能面临挑战。在本研究中,我们开发了一种自支撑双功能Pt/SnO/NbO/Nb电催化剂,该催化剂能够在酸性介质中将析氢反应与选择性乙醇氧化反应(EOR)耦合。该催化剂对EOR显示出有效性,相对于标准氢电极(SHE)为+130 mV时,峰值电流密度为8.97 mA/cm²。该双功能电催化剂对析氢反应(HER)表现出电流的自发快速增加,在电流密度为5 mA/cm²时过电位为-48 mV,法拉第效率为99.7%。与传统的水分解相比,EOR与HER的这种有效耦合降低了绿色氢能生产的能耗。由于氢气是唯一的气态产物,HER-EOR电解系统无需隔膜即可有效运行,有望实现更具成本效益、可持续且高效的绿色氢能生产。