Lanthanide metal-assisted synthesis of rhombic dodecahedral MNi (M = Ir and Pt) nanoframes toward efficient oxygen evolution catalysis

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Nano Energy, ISSN: 2211-2855, Vol: 42, Page: 17-25

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Jin, Haneul; Hong, Yongju; Yoon, Jisun; Oh, Aram; Chaudhari, Nitin K.; Baik, Hionsuck; Joo, Sang Hoon; Lee, Kwangyeol
Elsevier BV
Energy; Materials Science; Engineering; Water electrolyzer; Iridium; Catalysis; Nanoframe; Grain boundary
article description
Mixed metal alloy nanoframeworks have shown a great promise as electrocatalysts in water electrolyzers and fuel cells. Although a limited number of mixed metal alloy nanoframeworks have been synthesized through phase segregation of alloy phases and removal of a component, there remains a strong need for a straightforward and facile synthesis route to this important nanostructure. A wide avenue for nanoframework structures can be opened with a fail-proof method for edge-coating shape-controlled template nanoparticles. Herein, we demonstrate that lanthanide metal chlorides can selectively passivate facets of a Ni nanotemplate, leaving the edges for the growth of a secondary metal (M = Ir, Pt). The edge-deposited metal can be further in situ mixed with the underlying Ni phase to afford rhombic dodecahedral nanoframes of binary alloy phases, namely, IrNi (IrNi-RF) and PtNi (PtNi-RF). IrNi-RF showed excellent electrocatalytic activity for the oxygen evolution reaction (OER) in an acidic electrolyte, requiring and overpotential of only 313.6 mV at 10 mA cm −2. Furthermore, even after 5000 potential cycles in the OER, IrNi-RF underwent little performance loss with an overpotential of 329.3 mV at 10 mA cm −2, demonstrating excellent catalytic stability. The presence of highly active grain boundaries, agglomeration-free frame structures, as well as the presence of IrNi/IrO x interface might be responsible for the excellent electrocatalytic activity and stability.