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Bimetallic PtCu-decorated reduced graphene oxide (RGO)-TiO2 nanocomposite for efficient oxygen reduction reaction
被引:20
作者:
Sravani, B.
[1
]
Chandrashekar, Y.
[1
]
Chandana, P. Sri
[2
]
Maiyalagan, T.
[3
]
Sarma, L. Subramanyam
[1
]
机构:
[1] Yogi Vemana Univ, Dept Chem, Nanoelectrochem Lab, Kadapa 516005, Andhra Pradesh, India
[2] Annamacharya Inst Sci & Technol, Dept Civil & Environm Engn, Kadapa 516003, Andhra Pradesh, India
[3] SRM Inst Sci & Technol, Dept Chem, Electrochem Energy Lab, Kattankulathur 603203, Tamil Nadu, India
关键词:
Methanol oxidation reaction (MOR);
Oxygen reduction reaction (ORR);
METAL-FREE ELECTROCATALYSTS;
HIGH-PERFORMANCE;
PARTICLE-SIZE;
CARBON;
NANOPARTICLES;
NITROGEN;
CATALYSTS;
ALLOY;
TIO2;
D O I:
10.1016/j.synthmet.2020.116433
中图分类号:
T [工业技术];
学科分类号:
08 ;
摘要:
To exploit the full advantages of electrocatalysts for fuel cell reactions, a promising support is essential to disperse electrocatalytically active metal nanoparticles. Here, at first a graphene oxide-titanium dioxide composite support (GO-TiO2) is fabricated by a sol-gel method. Later, a facile chemical reduction method is demonstrated to simultaneously reduce Pt4+ , Cu2+ and GO-TiO2 to form bimetallic PtCu nanoparticles (15 wt% Pt + 5 wt% Cu) on a reduced graphene oxide-titanium dioxide (RGO-TiO2) composite support. A combined action of ethylene glycol and ascorbic acid play a positive role in attaining well dispersed PtCu with a size of 7 nm particles on RGO-TiO2 sheets. The resulting PtCu/RGO-TiO2 nanocomposite exhibits superior electrode-area normalized ORR limiting current density (6.14 mA/cm(2)-geo) when compared to commercial PVC (3.61 mA/cm(2)-geo) and in-house synthesized PtCu/RGO (4.68 mA/cm(2)-geo) and Pt/RGO (3.95 mA/cm(2)-geo) catalysts. The synthesized catalysts are characterized for structural, morphological and surface elemental features by using a combination of diffraction, spectroscopy and electron microscopy techniques. The positive role played by PtCu and RGO-TiO2 composite support assists the improved ORR activity. The versatile synthesis methodology presented here is convenient to fabricate other similar electrocatalytic nanostructures for fuel cell reactions.
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