Ruthenium Core–Shell Engineering with Nickel Single Atoms for Selective Oxygen Evolution via Nondestructive Mechanism. Issue 10 (25th January 2021)

• Record Type: Journal Article
• Authors: Harzandi, Ahmad M.; Shadman, Sahar; Nissimagoudar, Arun S.; Kim, Dong Yeon; Lim, Hee‐Dae; Lee, Jong Hoon; Kim, Min Gyu; Jeong, Hu Young; Kim, Youngsik; Kim, Kwang S.
• Is Part Of: Advanced energy materials. Volume 11:Issue 10(2021)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2021-01-25
• Subjects: lattice oxygen -- leaching -- mechanism -- nickel -- oxygen evolution reaction -- ruthenium -- surface engineering; Energy harvesting -- Materials -- Periodicals; Energy conversion -- Materials -- Periodicals; Energy storage -- Materials -- Periodicals; Photovoltaics -- Periodicals; Fuel cells -- Periodicals; Thermoelectric materials -- Periodicals; 621.31
• DOI: 10.1002/aenm.202003448
• Languages: English
• ISSNs: 1614-6832

Abstract

Abstract: To develop effective electrocatalytic splitting of acidic water, which is a key reaction for renewable energy conversion, the fundamental understanding of sluggish/destructive mechanism of the oxygen evolution reaction (OER) is essential. Through investigating atom/proton/electron transfers in the OER, the distinctive acid–base (AB) and direct‐coupling (DC) lattice oxygen mechanisms (LOMs) and adsorbates evolution mechanism (AEM) are elucidated, depending on the surface‐defect engineering condition. The designed catalysts are composed of a compressed metallic Ru‐core and oxidized Ru‐shell with Ni single atoms (SAs). The catalyst synthesized with hot acid treatment selectively follows AB‐LOM, exhibiting simultaneously enhanced activity and stability. It produces a current density of 10/100 mA cm −2 at a low overpotential of 184/229 mV and sustains water oxidation at a high current density of up to 20 mA cm −2 over ≈200 h in strongly acidic media. Abstract : The surface engineered catalyst of Ni‐Ru@RuO x ‐HL accelerates oxygen production via an acid‐based mechanism that involves one oxygen atom from the lattice and one oxygen atom from the electrolyte which boosts oxygen evolution reaction activity. Prohibited direct coupling of lattice oxygens causes durable performance for this catalyst.