Enhanced electrocatalytic nitrate reduction by preferentially-oriented (100) PtRh and PtIr alloys: the hidden treasures of the 'miscibility gap'

被引:55
作者
Duca, Matteo [1 ]
Sacre, Nicolas [1 ]
Wang, Andrew [1 ,2 ]
Garbarino, Sebastien [1 ]
Guay, Daniel [1 ]
机构
[1] Inst Natl Rech Sci, INRS Energie Mat & Telecommun, 1650 Blvd Lionel Boulet, Varennes, PQ J3X 1S2, Canada
[2] Univ British Columbia, Dept Chem, 2036 Main Mall, Vancouver, BC V6T 1Z1, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Nitrate reduction; Epitaxial films; Alloys; Electrocatalysis; (100) surfaces; MONOCRYSTALLINE IRIDIUM SURFACES; ZERO CHARGE POTENTIALS; NITRIC-OXIDE; ELECTROCHEMICAL CHARACTERIZATION; CARBON-MONOXIDE; THIN-FILMS; METHANOL ELECTROOXIDATION; CATALYTIC-ACTIVITY; ADSORPTION; PLATINUM;
D O I
10.1016/j.apcatb.2017.08.081
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Bimetallic alloys of Pt and Rh or Ir were prepared with pulsed laser deposition (PLD) on a well-ordered MgO (100) substrate, leading to epitaxial growth along the [001] plane, as confirmed by surface analysis techniques. The out-of-equilibrium conditions of PLD allowed the exploration of a range of compositions for which phase separation would instead be expected. The electrochemistry of a series of PtRh and PtIr (100) alloys was investigated in 0.5 M H2SO4, showing a surprisingly intense electrocatalytic activity towards the reduction of nitrate for a Pt content of 21-42%. These alloys feature a lower reaction overpotential with respect to Rh and Jr while outperforming the pure metals in terms of reduction current. A detailed analysis of the voltammetric features with respect to alloy composition highlighted a correlation between hydrogen desorption and nitrate reduction activity. In addition, an optimal potential range for nitrate reduction, common to PtRh and air alloys, was observed, corresponding to the potential window in which nitrate adsorption coincides with fast reduction of the key reaction intermediate NOads.
引用
收藏
页码:86 / 96
页数:11
相关论文
共 64 条
[11]   Thirty years of platinum single crystal electrochemistry [J].
Climent, V. ;
Feliu, Juan M. .
JOURNAL OF SOLID STATE ELECTROCHEMISTRY, 2011, 15 (7-8) :1297-1315
[12]   The role of adsorbates in the electrochemical oxidation of ammonia on noble and transition metal electrodes [J].
de Vooys, ACA ;
Koper, MTM ;
van Santen, RA ;
van Veen, JAR .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2001, 506 (02) :127-137
[13]   Mechanistic study on the electrocatalytic reduction of nitric oxide on transition-metal electrodes [J].
de Vooys, ACA ;
Koper, MTM ;
van Santen, RA ;
van Veen, JAR .
JOURNAL OF CATALYSIS, 2001, 202 (02) :387-394
[14]   Nitrate reduction on single-crystal platinum electrodes [J].
Dima, GE ;
Beltramo, GL ;
Koper, MTM .
ELECTROCHIMICA ACTA, 2005, 50 (21) :4318-4326
[15]   Electrocatalytic reduction of nitrate at low concentration on coinage and transition-metal electrodes in acid solutions [J].
Dima, GE ;
de Vooys, ACA ;
Koper, MTM .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2003, 554 :15-23
[16]   Electrocatalytic reduction of nitrite on transition and coinage metals [J].
Duca, M. ;
van der Klugt, B. ;
Koper, M. T. M. .
ELECTROCHIMICA ACTA, 2012, 68 :32-43
[17]   Electrocatalytic reduction of nitrite on a polycrystalline rhodium electrode [J].
Duca, M. ;
van der Klugt, B. ;
Hasnat, M. A. ;
Machida, M. ;
Koper, M. T. M. .
JOURNAL OF CATALYSIS, 2010, 275 (01) :61-69
[18]   New insights into the mechanism of nitrite reduction on a platinum electrode [J].
Duca, M. ;
Kavvadia, V. ;
Rodriguez, P. ;
Lai, S. C. S. ;
Hoogenboom, T. ;
Koper, M. T. M. .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2010, 649 (1-2) :59-68
[19]   Combining Noble Metals and Enzymes for Relay Cascade Electrocatalysis of Nitrate Reduction to Ammonia at Neutral pH [J].
Duca, Matteo ;
Weeks, Justin R. ;
Fedor, Justin G. ;
Weiner, Joel H. ;
Vincent, Kylie A. .
CHEMELECTROCHEM, 2015, 2 (08) :1086-1089
[20]   Powering denitrification: the perspectives of electrocatalytic nitrate reduction [J].
Duca, Matteo ;
Koper, Marc T. M. .
ENERGY & ENVIRONMENTAL SCIENCE, 2012, 5 (12) :9726-9742