Au-Manganese Oxide Nanostructures by a Plasma-Assisted Process as Electrocatalysts for Oxygen Evolution: A Chemico-Physical Investigation

被引:8
作者
Bigiani, Lorenzo [1 ,2 ]
Gasparotto, Alberto [1 ,2 ]
Andreu, Teresa [3 ,4 ]
Verbeeck, Johan [5 ,6 ]
Sada, Cinzia [2 ,7 ]
Modin, Evgeny [8 ]
Lebedev, Oleg I. [9 ]
Morante, Juan Ramon [3 ,4 ]
Barreca, Davide [10 ,11 ]
Maccato, Chiara [1 ,2 ]
机构
[1] Padova Univ, Dept Chem Sci, I-35131 Padua, Italy
[2] INSTM, I-35131 Padua, Italy
[3] Catalonia Inst Energy Res IREC, Barcelona 08930, Spain
[4] Univ Barcelona UB, Barcelona 08028, Spain
[5] Univ Antwerp, EMAT, B-2020 Antwerp, Belgium
[6] Univ Antwerp, NANOlab Ctr Excellence, B-2020 Antwerp, Belgium
[7] Padova Univ, Dept Phys & Astron, I-35131 Padua, Italy
[8] CIC NanoGUNE BRTA, Donostia San Sebastian 20018, Spain
[9] UCBN, Lab CRISMAT, UMR 6508, CNRS,ENSICAEN, F-14050 Caen 4, France
[10] Padova Univ, Dept Chem Sci, CNR ICMATE, I-35131 Padua, Italy
[11] Padova Univ, Dept Chem Sci, INSTM, I-35131 Padua, Italy
基金
欧盟地平线“2020”;
关键词
manganese oxides; oxygen evolution reaction; strong metal-support interaction; METAL-SUPPORT INTERACTION; ELECTROCHEMICAL WATER OXIDATION; ATOMIC LAYER DEPOSITION; HIGHLY EFFICIENT; THIN-FILMS; CATALYTIC-ACTIVITY; REDUCTION; GROWTH; GOLD; NANOPARTICLES;
D O I
10.1002/adsu.202000177
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Earth-abundant and eco-friendly manganese oxides are promising platforms for the oxygen evolution reaction (OER) in water electrolysis. Herein, a versatile and potentially scalable route to gold-decorated manganese oxide-based OER electrocatalysts is reported. In particular, MnxOy(MnO2, Mn2O3) host matrices are grown on conductive glasses by plasma assisted-chemical vapor deposition (PA-CVD), and subsequently functionalized with gold nanoparticles (guest) as OER activators by radio frequency (RF)-sputtering. The final selective obtainment of MnO2- or Mn2O3-based systems is then enabled by annealing under oxidizing or inert atmosphere, respectively. A detailed material characterization evidences the formation of high-purity Mn(x)O(y)dendritic nanostructures with an open morphology and an efficient guest dispersion into the host matrices. The tailoring of Mn(x)O(y)phase composition and host-guest interactions has a remarkable influence on OER activity yielding, for the best performing Au/Mn(2)O(3)system, a current density of approximate to 5 mA cm(-2)at 1.65 V versus the reversible hydrogen electrode (RHE) and an overpotential close to 300 mV at 1 mA cm(-2). Such results, comparing favorably with literature data on manganese oxide-based materials, highlight the importance of compositional control, as well as of surface and interface engineering, to develop low-cost and efficient anode nanocatalysts for water splitting applications.
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页数:11
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