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Tryptophan-Stabilized Au-Fe_xO_y Nanocomposites as Electrocatalysts for Oxygen Evolution Reaction.

ABSTRACT: Au-Fe_xO_y nanocomposites with a variable gold-to-iron ratio were stabilized with l-tryptophan. The synthetic methodology is based on the facile redox reaction between Au(III) and Fe(0) in the presence of gold nanoparticle as a seed at room temperature in an aqueous medium. The synthesis results in the deposition of Au nanoparticles on the surface of iron oxide layers. Composition variation in the nanocomposites was obtained by controlling the seed amount and reducing agent. These nanocomposites are used as electrocatalysts for the thermodynamically unfavorable oxygen evolution reaction (OER) from water. Among the nanocomposites, the most efficient OER activity was observed from the nanocomposite 12. The content of iron with respect to gold is at the maximum in the nanocomposite, which was obtained from the reaction with a minimum seed concentration and maximum reducing agent.

SUBMITTER: Lone SA

PROVIDER: S-EPMC6647969 | biostudies-literature | 2019 Feb

REPOSITORIES: biostudies-literature

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Tryptophan-Stabilized Au-FexOy Nanocomposites as Electrocatalysts for Oxygen Evolution Reaction.

Lone Shahbaz Ahmad SA Ghosh Soumen S Sadhu Kalyan K KK

ACS omega 20190214 2

Au-FexOy nanocomposites with a variable gold-to-iron ratio were stabilized with l-tryptophan. The synthetic methodology is based on the facile redox reaction between Au(III) and Fe(0) in the presence of gold nanoparticle as a seed at room temperature in an aqueous medium. The synthesis results in the deposition of Au nanoparticles on the surface of iron oxide layers. Composition variation in the nanocomposites was obtained by controlling the seed amount and reducing agent. ...[more]

PMID: 31459553

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Project description:Metal-organic frameworks (MOFs) have been investigated with regard to the oxygen evolution reaction (OER) due to their structure diversity, high specific surface area, adjustable pore size, and abundant active sites. However, the poor conductivity of most MOFs restricts this application. Herein, through a facile one-step solvothermal method, the Ni-based pillared metal-organic framework [Ni2(BDC)2DABCO] (BDC = 1,4-benzenedicarboxylate, DABCO = 1,4-diazabicyclo[2.2.2]octane), its bimetallic nickel-iron form [Ni(Fe)(BDC)2DABCO], and their modified Ketjenblack (mKB) composites were synthesized and tested toward OER in an alkaline medium (KOH 1 mol L-1). A synergistic effect of the bimetallic nickel-iron MOF and the conductive mKB additive enhanced the catalytic activity of the MOF/mKB composites. All MOF/mKB composite samples (7, 14, 22, and 34 wt.% mKB) indicated much higher OER performances than the MOFs and mKB alone. The Ni-MOF/mKB14 composite (14 wt.% of mKB) demonstrated an overpotential of 294 mV at a current density of 10 mA cm-2 and a Tafel slope of 32 mV dec-1, which is comparable with commercial RuO2, commonly used as a benchmark material for OER. The catalytic performance of Ni(Fe)MOF/mKB14 (0.57 wt.% Fe) was further improved to an overpotential of 279 mV at a current density of 10 mA cm-2. The low Tafel slope of 25 mV dec-1 as well as a low reaction resistance due to the electrochemical impedance spectroscopy (EIS) measurement confirmed the excellent OER performance of the Ni(Fe)MOF/mKB14 composite. For practical applications, the Ni(Fe)MOF/mKB14 electrocatalyst was impregnated into commercial nickel foam (NF), where overpotentials of 247 and 291 mV at current densities of 10 and 50 mA cm-2, respectively, were realized. The activity was maintained for 30 h at the applied current density of 50 mA cm-2. More importantly, this work adds to the fundamental understanding of the in situ transformation of Ni(Fe)DMOF into OER-active α/β-Ni(OH)2, β/γ-NiOOH, and FeOOH with residual porosity inherited from the MOF structure, as seen by powder X-ray diffractometry and N2 sorption analysis. Benefitting from the porosity structure of the MOF precursor, the nickel-iron catalysts outperformed the solely Ni-based catalysts due to their synergistic effects and exhibited superior catalytic activity and long-term stability in OER. In addition, by introducing mKB as a conductive carbon additive in the MOF structure, a homogeneous conductive network was constructed to improve the electronic conductivity of the MOF/mKB composites. The electrocatalytic system consisting of earth-abundant Ni and Fe metals only is attractive for the development of efficient, practical, and economical energy conversion materials for efficient OER activity.

Dataset Information

Tryptophan-Stabilized Au-Fe_xO_y Nanocomposites as Electrocatalysts for Oxygen Evolution Reaction.

Publications

Tryptophan-Stabilized Au-Fe<sub>x</sub>O<sub>y</sub> Nanocomposites as Electrocatalysts for Oxygen Evolution Reaction.

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