| Autor: |
HandokoThese authors contributed equally., Albertus D., Deng, Suzi, Deng, Yilin, Cheng, Andy Wing Fai, Chan, Kuang Wen, Tan, Hui Ru, Pan, Yanlin, Tok, Eng Soon, Sow, Chorng Haur, Yeo, Boon Siang |
| Zdroj: |
Catalysis Science & Technology; 2015, Vol. 6 Issue: 1 p269-274, 6p |
| Abstrakt: |
The successful design and synthesis of earth-abundant and efficient catalysts for the oxygen evolution reaction (OER) will be a major step forward towards the use of electrochemical water splitting as an environmentally-friendly process for producing H2fuel. Due to their poor activity, copper-based materials have not been considered apt for catalysing OER. In this work, we demonstrate that unique copper(ii) oxide nanostructures obtained viahydrothermal synthesis and subsequent hydrogen peroxide treatment exhibit unusually high and sustainable OER activity. In 0.1 M KOH electrolyte, the CuO nanostructures catalyse OER with current densities of 2.6–3.4 mA cm−2at 1.75 V (vs.RHE). The calculated turnover frequency (per Cu site) of ~2 × 10−3s−1for O2production is markedly higher than that of high-surface area electrodeposited Cu metal nanoparticles by 40–68 times. The OER activity of the CuO nanostructures is also stable, approaching about half of 20% IrOx/Vulcan XC-72 after an hour-long OER. In situRaman spectroscopy at OER-relevant potentials recorded compelling evidence that CuIIIactive species may be responsible for the unusual OER activity of the CuO nanostructures, as indicated by its signature vibration at 603 cm−1. This hitherto unobserved peak is assigned, with the aid of the model compound NaCuIIIO2, to the Cu–O stretching vibration of CuIIIoxide. This feature was not found on electrodeposited Cu metal, which exhibited correspondingly weaker OER activity. The enhanced catalysis of O2evolution by the CuO nanostructures is thus attributed to not just their higher surface area, but also the higher population of CuIIIactive sites on their surface. |
| Databáze: |
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