The development of cheap and efficient catalysts for the oxygen evolution reaction (OER) plays a critical role for sustainable energy conversion and storage. Herein, we report on Mn2O3-based systems supported on nickel foams and functionalized with first-row transition-metal (Fe, Co, Ni) oxide nanoparticles (NPs) as OER electrocatalysts in alkaline media, fabricated by a plasma-assisted process. The remarkable substrate porosity and high Mn2O3 active area, due to the quasi-onedimensional nano-organization, enabled an efficient ultradispersion of Fe2O3, Co3O4, and NiO NPs into Mn2O3 and an intimate oxide-oxide interfacial contact, enhancing thus charge carrier transport and facilitating reactants and products diffusion. Among the developed systems, Fe2O3-Mn2O3 yielded the highest electrocatalytic activity, corresponding to a low overpotential of similar to 350 mV at 10 mA x cm(-2) and a Tafel slope of 70 mV x dec(-1), allowing high current density values. The obtained performances, discussed in relation to the material properties, are superior to almost all the state-of-the-art manganese oxide catalysts and compare favorably with various noble-metal-based systems, paving the way to additional activity improvements via compositional and interfacial engineering.
Quasi-1D Mn2O3 nanostructures functionalized with first-row transition metal oxides as oxygen evolution catalysts
	
	
	
		
		
		
		
		
	
	
	
	
	
	
	
	
		
		
		
		
		
			
			
			
		
		
		
		
			
			
				
				
					
					
					
					
						
							
						
						
					
				
				
				
				
				
				
				
				
				
				
				
			
			
		
			
			
				
				
					
					
					
					
						
							
						
						
					
				
				
				
				
				
				
				
				
				
				
				
			
			
		
			
			
				
				
					
					
					
					
						
						
							
							
						
					
				
				
				
				
				
				
				
				
				
				
				
			
			
		
			
			
				
				
					
					
					
					
						
							
						
						
					
				
				
				
				
				
				
				
				
				
				
				
			
			
		
			
			
				
				
					
					
					
					
						
							
						
						
					
				
				
				
				
				
				
				
				
				
				
				
			
			
		
			
			
				
				
					
					
					
					
						
						
							
							
						
					
				
				
				
				
				
				
				
				
				
				
				
			
			
		
			
			
				
				
					
					
					
					
						
						
							
							
						
					
				
				
				
				
				
				
				
				
				
				
				
			
			
		
			
			
				
				
					
					
					
					
						
						
							
							
						
					
				
				
				
				
				
				
				
				
				
				
				
			
			
		
			
			
				
				
					
					
					
					
						
							
						
						
					
				
				
				
				
				
				
				
				
				
				
				
			
			
		
		
		
		
	
Lorenzo Bigiani;Chiara Maccato
;Alberto Gasparotto;Cinzia Sada;Davide Barreca
	
		
		
	
			2020
Abstract
The development of cheap and efficient catalysts for the oxygen evolution reaction (OER) plays a critical role for sustainable energy conversion and storage. Herein, we report on Mn2O3-based systems supported on nickel foams and functionalized with first-row transition-metal (Fe, Co, Ni) oxide nanoparticles (NPs) as OER electrocatalysts in alkaline media, fabricated by a plasma-assisted process. The remarkable substrate porosity and high Mn2O3 active area, due to the quasi-onedimensional nano-organization, enabled an efficient ultradispersion of Fe2O3, Co3O4, and NiO NPs into Mn2O3 and an intimate oxide-oxide interfacial contact, enhancing thus charge carrier transport and facilitating reactants and products diffusion. Among the developed systems, Fe2O3-Mn2O3 yielded the highest electrocatalytic activity, corresponding to a low overpotential of similar to 350 mV at 10 mA x cm(-2) and a Tafel slope of 70 mV x dec(-1), allowing high current density values. The obtained performances, discussed in relation to the material properties, are superior to almost all the state-of-the-art manganese oxide catalysts and compare favorably with various noble-metal-based systems, paving the way to additional activity improvements via compositional and interfacial engineering.| File | Dimensione | Formato | |
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