A Facile Synthesis of MPd (M = Co, Cu) Nanoparticles and Their Catalysis for Formic Acid Oxidation

Monodisperse CoPd nanoparticles (NPs) were synthesized and studied for catalytic formic acid (HCOOH) oxidation (FAO). The NPs were prepared by coreduction of Co(acac)2 (acac = acetylacetonate) and PdBr2 at 260 °C in oleylamine and trioctylphosphine, and their sizes (5–12 nm) and compositions (Co10Pd...

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Veröffentlicht in:Nano letters 2012-02, Vol.12 (2), p.1102-1106
Hauptverfasser: Mazumder, Vismadeb, Chi, Miaofang, Mankin, Max N, Liu, Yi, Metin, Önder, Sun, Daohua, More, Karren L, Sun, Shouheng
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container_end_page 1106
container_issue 2
container_start_page 1102
container_title Nano letters
container_volume 12
creator Mazumder, Vismadeb
Chi, Miaofang
Mankin, Max N
Liu, Yi
Metin, Önder
Sun, Daohua
More, Karren L
Sun, Shouheng
description Monodisperse CoPd nanoparticles (NPs) were synthesized and studied for catalytic formic acid (HCOOH) oxidation (FAO). The NPs were prepared by coreduction of Co(acac)2 (acac = acetylacetonate) and PdBr2 at 260 °C in oleylamine and trioctylphosphine, and their sizes (5–12 nm) and compositions (Co10Pd90 to Co60Pd40) were controlled by heating ramp rate, metal salt concentration, or metal molar ratios. The 8 nm CoPd NPs were activated for HCOOH oxidation by a simple ethanol wash. In 0.1 M HClO4 and 2 M HCOOH solution, their catalytic activities followed the trend of Co50Pd50 > Co60Pd40 > Co10Pd90 > Pd. The Co50Pd50 NPs had an oxidation peak at 0.4 V with a peak current density of 774 A/gPd. As a comparison, commercial Pd catalysts showed an oxidation peak at 0.75 V with peak current density of only 254 A/gPd. The synthesis procedure could also be extended to prepare CuPd NPs when Co(acac)2 was replaced by Cu(ac)2 (ac = acetate) in an otherwise identical condition. The CuPd NPs were less active catalysts than CoPd or even Pd for FAO in HClO4 solution. The synthesis provides a general approach to Pd-based bimetallic NPs and will enable further investigation of Pd-based alloy NPs for electro-oxidation and other catalytic reactions.
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The synthesis procedure could also be extended to prepare CuPd NPs when Co(acac)2 was replaced by Cu(ac)2 (ac = acetate) in an otherwise identical condition. The CuPd NPs were less active catalysts than CoPd or even Pd for FAO in HClO4 solution. 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(ORNL), Oak Ridge, TN (United States)</creatorcontrib><title>A Facile Synthesis of MPd (M = Co, Cu) Nanoparticles and Their Catalysis for Formic Acid Oxidation</title><title>Nano letters</title><addtitle>Nano Lett</addtitle><description>Monodisperse CoPd nanoparticles (NPs) were synthesized and studied for catalytic formic acid (HCOOH) oxidation (FAO). The NPs were prepared by coreduction of Co(acac)2 (acac = acetylacetonate) and PdBr2 at 260 °C in oleylamine and trioctylphosphine, and their sizes (5–12 nm) and compositions (Co10Pd90 to Co60Pd40) were controlled by heating ramp rate, metal salt concentration, or metal molar ratios. The 8 nm CoPd NPs were activated for HCOOH oxidation by a simple ethanol wash. In 0.1 M HClO4 and 2 M HCOOH solution, their catalytic activities followed the trend of Co50Pd50 &gt; Co60Pd40 &gt; Co10Pd90 &gt; Pd. The Co50Pd50 NPs had an oxidation peak at 0.4 V with a peak current density of 774 A/gPd. 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(ORNL), Oak Ridge, TN (United States)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Facile Synthesis of MPd (M = Co, Cu) Nanoparticles and Their Catalysis for Formic Acid Oxidation</atitle><jtitle>Nano letters</jtitle><addtitle>Nano Lett</addtitle><date>2012-02-08</date><risdate>2012</risdate><volume>12</volume><issue>2</issue><spage>1102</spage><epage>1106</epage><pages>1102-1106</pages><issn>1530-6984</issn><eissn>1530-6992</eissn><abstract>Monodisperse CoPd nanoparticles (NPs) were synthesized and studied for catalytic formic acid (HCOOH) oxidation (FAO). The NPs were prepared by coreduction of Co(acac)2 (acac = acetylacetonate) and PdBr2 at 260 °C in oleylamine and trioctylphosphine, and their sizes (5–12 nm) and compositions (Co10Pd90 to Co60Pd40) were controlled by heating ramp rate, metal salt concentration, or metal molar ratios. The 8 nm CoPd NPs were activated for HCOOH oxidation by a simple ethanol wash. In 0.1 M HClO4 and 2 M HCOOH solution, their catalytic activities followed the trend of Co50Pd50 &gt; Co60Pd40 &gt; Co10Pd90 &gt; Pd. The Co50Pd50 NPs had an oxidation peak at 0.4 V with a peak current density of 774 A/gPd. As a comparison, commercial Pd catalysts showed an oxidation peak at 0.75 V with peak current density of only 254 A/gPd. The synthesis procedure could also be extended to prepare CuPd NPs when Co(acac)2 was replaced by Cu(ac)2 (ac = acetate) in an otherwise identical condition. The CuPd NPs were less active catalysts than CoPd or even Pd for FAO in HClO4 solution. The synthesis provides a general approach to Pd-based bimetallic NPs and will enable further investigation of Pd-based alloy NPs for electro-oxidation and other catalytic reactions.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>22276672</pmid><doi>10.1021/nl2045588</doi><tpages>5</tpages></addata></record>
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1530-6992
language eng
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source MEDLINE; ACS Publications
subjects Acetates
ALLOYS
Alloys - chemical synthesis
Alloys - chemistry
CATALYSIS
CATALYSTS
Catalysts: preparations and properties
Chemistry
Cobalt - chemistry
Copper - chemistry
CURRENT DENSITY
ETHANOL
Exact sciences and technology
Formates - chemistry
FORMIC ACID
General and physical chemistry
HEATING
Metal Nanoparticles - chemistry
Nanoparticles
NANOSCIENCE AND NANOTECHNOLOGY
OXIDATION
Oxidation-Reduction
Palladium
Palladium - chemistry
Particle Size
Surface Properties
SYNTHESIS
Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry
title A Facile Synthesis of MPd (M = Co, Cu) Nanoparticles and Their Catalysis for Formic Acid Oxidation
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