4.8 Article

Iridium-Based Multimetallic Nanoframe@Nanoframe Structure: An Efficient and Robust Electrocatalyst toward Oxygen Evolution Reaction

Journal

ACS NANO
Volume 11, Issue 6, Pages 5500-5509

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.7b00233

Keywords

nanoframe; kinetic control; iridium-based nanocrystal; ternary alloy; electrocatalysis; oxygen evolution reaction

Funding

  1. Korea University Future Research Grant
  2. Global Ph.D. Fellowship [NRF-2013H1A2A1032644]
  3. [IBS-R023-D1]
  4. [NRF-2017R1A2B3005682]
  5. [NRF- 2017R1A2B2008464]

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Nanoframe electrocatalysts have attracted great interest due to their inherently high active surface area per a given mass. Although recent progress has enabled the preparation of single nanoframe structures with a variety of morphologies, more complex nanoframe structures such as a double-layered nanoframe have not yet been realized. Herein, we report a rational synthetic strategy for a structurally robust Ir-based multimetallic double-layered nanoframe (DNF) structure, nanoframe@nanoframe. By leveraging the differing kinetics of dual Ir precursors and dual transition metal (Ni and Cu) precursors, a core shell-type alloy@alloy structure could be generated in a simple one-step synthesis, which was subsequently transformed into a multimetallic IrNiCu DNF with a rhombic dodecahedral morphology via selective etching. The use of single Ir precursor yielded single nanoframe structures, highlighting the importance of employing dual Ir precursors. In addition, the structure of Ir-based nanocrystals could be further controlled to DNF with octahedral morphology and CuNi@Ir core shell structures via a simple tuning of experimental factors. The IrNiCu DNF exhibited high electrocatalytic activity for oxygen evolution reaction (OER) in acidic media, which is better than Ir/C catalyst. Furthermore, IrNiCu DNF demonstrated excellent durability for OER, which could be attributed to the frame structure that prevents the growth and agglomeration of particles as well as in situ formation of robust rutile II, phase during prolonged operation.

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