Pt-loaded Au@CeO2 core-shell nanocatalysts for improving methanol oxidation reaction activity

Dung Van Dao, Thanh Duc Le, Ganpurev Adilbish, In Hwan Lee, Yeon Tae Yu

Research output: Contribution to journalArticle

Abstract

Herein, we provide a facile hydrothermal process for ultralow Pt loading (3.84 wt%) on the porous surface of an Au@CeO2 core-shell nanocatalyst (CSNC) in order to improve the electrocatalytic property of bare Pt towards the methanol oxidation reaction (MOR). The Au@CeO2@Pt CSNC demonstrated a high BET surface area (88.10 m2 g-1) and high numbers of catalytic surface active species (such as Pt0, Ce3+ and oxygen vacancies). The corresponding electrode obtained by spraying the Au@CeO2@Pt CSNC onto the microporous layer (MPL) of carbon cloth (Au@CeO2@Pt/C) showed better electrocatalytic properties, such as high electrochemical surface area (ECSA-80 m2 g-1) and low charge transfer resistance (37 Ω) than CeO2@Pt/C (52 m2 g-1 and 106 Ω) and commercial Pt/C (44 m2 g-1 and 182 Ω). Furthermore, the positive catalytic properties of the Au@CeO2@Pt/C electrode were investigated via MOR mass activity which at 1.36 A mgPt-1, was 1.5 and 2.0 times higher than those obtained from the CeO2@Pt/C (0.92 A mgPt-1) and commercial Pt/C (0.67 A mgPt-1) electrodes, respectively. Moreover, the Au@CeO2@Pt/C electrocatalyst also had good MOR durability and high CO tolerance. The electrocatalytic enhancement of the Au@CeO2@Pt CSNC could be the result of the electronic, bifunctional and synergistic effects between the Au, CeO2 and Pt components supported on the carbon cloth. Accordingly, these advantageous effects easily removed the adsorbed CO intermediate as the main poisoner on the surface of the Pt catalyst, and thereby significantly improved the overall MOR activity.

Original languageEnglish
Pages (from-to)26996-27006
Number of pages11
JournalJournal of Materials Chemistry A
Volume7
Issue number47
DOIs
Publication statusPublished - 2019 Jan 1

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Methanol
Oxidation
Carbon Monoxide
Electrodes
Carbon
Electrocatalysts
Poisons
Oxygen vacancies
Spraying
Charge transfer
Durability
Catalysts

ASJC Scopus subject areas

  • Chemistry(all)
  • Renewable Energy, Sustainability and the Environment
  • Materials Science(all)

Cite this

Pt-loaded Au@CeO2 core-shell nanocatalysts for improving methanol oxidation reaction activity. / Dao, Dung Van; Le, Thanh Duc; Adilbish, Ganpurev; Lee, In Hwan; Yu, Yeon Tae.

In: Journal of Materials Chemistry A, Vol. 7, No. 47, 01.01.2019, p. 26996-27006.

Research output: Contribution to journalArticle

Dao, Dung Van ; Le, Thanh Duc ; Adilbish, Ganpurev ; Lee, In Hwan ; Yu, Yeon Tae. / Pt-loaded Au@CeO2 core-shell nanocatalysts for improving methanol oxidation reaction activity. In: Journal of Materials Chemistry A. 2019 ; Vol. 7, No. 47. pp. 26996-27006.
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abstract = "Herein, we provide a facile hydrothermal process for ultralow Pt loading (3.84 wt{\%}) on the porous surface of an Au@CeO2 core-shell nanocatalyst (CSNC) in order to improve the electrocatalytic property of bare Pt towards the methanol oxidation reaction (MOR). The Au@CeO2@Pt CSNC demonstrated a high BET surface area (88.10 m2 g-1) and high numbers of catalytic surface active species (such as Pt0, Ce3+ and oxygen vacancies). The corresponding electrode obtained by spraying the Au@CeO2@Pt CSNC onto the microporous layer (MPL) of carbon cloth (Au@CeO2@Pt/C) showed better electrocatalytic properties, such as high electrochemical surface area (ECSA-80 m2 g-1) and low charge transfer resistance (37 Ω) than CeO2@Pt/C (52 m2 g-1 and 106 Ω) and commercial Pt/C (44 m2 g-1 and 182 Ω). Furthermore, the positive catalytic properties of the Au@CeO2@Pt/C electrode were investigated via MOR mass activity which at 1.36 A mgPt-1, was 1.5 and 2.0 times higher than those obtained from the CeO2@Pt/C (0.92 A mgPt-1) and commercial Pt/C (0.67 A mgPt-1) electrodes, respectively. Moreover, the Au@CeO2@Pt/C electrocatalyst also had good MOR durability and high CO tolerance. The electrocatalytic enhancement of the Au@CeO2@Pt CSNC could be the result of the electronic, bifunctional and synergistic effects between the Au, CeO2 and Pt components supported on the carbon cloth. Accordingly, these advantageous effects easily removed the adsorbed CO intermediate as the main poisoner on the surface of the Pt catalyst, and thereby significantly improved the overall MOR activity.",
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T1 - Pt-loaded Au@CeO2 core-shell nanocatalysts for improving methanol oxidation reaction activity

AU - Dao, Dung Van

AU - Le, Thanh Duc

AU - Adilbish, Ganpurev

AU - Lee, In Hwan

AU - Yu, Yeon Tae

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N2 - Herein, we provide a facile hydrothermal process for ultralow Pt loading (3.84 wt%) on the porous surface of an Au@CeO2 core-shell nanocatalyst (CSNC) in order to improve the electrocatalytic property of bare Pt towards the methanol oxidation reaction (MOR). The Au@CeO2@Pt CSNC demonstrated a high BET surface area (88.10 m2 g-1) and high numbers of catalytic surface active species (such as Pt0, Ce3+ and oxygen vacancies). The corresponding electrode obtained by spraying the Au@CeO2@Pt CSNC onto the microporous layer (MPL) of carbon cloth (Au@CeO2@Pt/C) showed better electrocatalytic properties, such as high electrochemical surface area (ECSA-80 m2 g-1) and low charge transfer resistance (37 Ω) than CeO2@Pt/C (52 m2 g-1 and 106 Ω) and commercial Pt/C (44 m2 g-1 and 182 Ω). Furthermore, the positive catalytic properties of the Au@CeO2@Pt/C electrode were investigated via MOR mass activity which at 1.36 A mgPt-1, was 1.5 and 2.0 times higher than those obtained from the CeO2@Pt/C (0.92 A mgPt-1) and commercial Pt/C (0.67 A mgPt-1) electrodes, respectively. Moreover, the Au@CeO2@Pt/C electrocatalyst also had good MOR durability and high CO tolerance. The electrocatalytic enhancement of the Au@CeO2@Pt CSNC could be the result of the electronic, bifunctional and synergistic effects between the Au, CeO2 and Pt components supported on the carbon cloth. Accordingly, these advantageous effects easily removed the adsorbed CO intermediate as the main poisoner on the surface of the Pt catalyst, and thereby significantly improved the overall MOR activity.

AB - Herein, we provide a facile hydrothermal process for ultralow Pt loading (3.84 wt%) on the porous surface of an Au@CeO2 core-shell nanocatalyst (CSNC) in order to improve the electrocatalytic property of bare Pt towards the methanol oxidation reaction (MOR). The Au@CeO2@Pt CSNC demonstrated a high BET surface area (88.10 m2 g-1) and high numbers of catalytic surface active species (such as Pt0, Ce3+ and oxygen vacancies). The corresponding electrode obtained by spraying the Au@CeO2@Pt CSNC onto the microporous layer (MPL) of carbon cloth (Au@CeO2@Pt/C) showed better electrocatalytic properties, such as high electrochemical surface area (ECSA-80 m2 g-1) and low charge transfer resistance (37 Ω) than CeO2@Pt/C (52 m2 g-1 and 106 Ω) and commercial Pt/C (44 m2 g-1 and 182 Ω). Furthermore, the positive catalytic properties of the Au@CeO2@Pt/C electrode were investigated via MOR mass activity which at 1.36 A mgPt-1, was 1.5 and 2.0 times higher than those obtained from the CeO2@Pt/C (0.92 A mgPt-1) and commercial Pt/C (0.67 A mgPt-1) electrodes, respectively. Moreover, the Au@CeO2@Pt/C electrocatalyst also had good MOR durability and high CO tolerance. The electrocatalytic enhancement of the Au@CeO2@Pt CSNC could be the result of the electronic, bifunctional and synergistic effects between the Au, CeO2 and Pt components supported on the carbon cloth. Accordingly, these advantageous effects easily removed the adsorbed CO intermediate as the main poisoner on the surface of the Pt catalyst, and thereby significantly improved the overall MOR activity.

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