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• W2413309827 endingPage "951" @default.
• W2413309827 startingPage "945" @default.
• W2413309827 abstract "Developing robust earth-abundant electrocatalysts for oxygen evolution reaction (OER) is an ongoing scientific challenge, which is coupled with a number of important electrochemical processes and many key renewable energy systems, such as water splitting, rechargeable metal-air batteries, and regenerative fuel cells. Here, we proposed a rational design and fabrication of the synergetic coaxial nanocable structures by intimate growth of the layered nickel-cobalt silicate hydroxide nanosheets on the outer surfaces of multiwalled carbon nanotubes (MWCNTs@NCS) and demonstrated their high efficiency in electrocatalytic OER from water splitting. The electrocatalytic activities of the MWCNTs@NCS were found to be significantly higher than that of bare NCS and pristine MWCNTs, synergetically determining by such the constituted individual components. Among them, the MWCNTs@NCS-2 exhibited best electrocatalytic OER performance, showing a small OER onset potential, large anodic current and long-term durability, which was favorably comparable to the previously reported NiCo-based OER electrocatalysts in alkaline electrolytes. To the best of our knowledge, this was a first example on the earth-abundant metal silicate hydroxides utilized in electrochemical water splitting." @default.
• W2413309827 created "2016-06-24" @default.
• W2413309827 creator A5019592083 @default.
• W2413309827 creator A5029349790 @default.
• W2413309827 creator A5031949860 @default.
• W2413309827 date "2015-12-29" @default.
• W2413309827 modified "2023-10-14" @default.
• W2413309827 title "When Layered Nickel–Cobalt Silicate Hydroxide Nanosheets Meet Carbon Nanotubes: A Synergetic Coaxial Nanocable Structure for Enhanced Electrocatalytic Water Oxidation" @default.
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• W2413309827 doi "https://doi.org/10.1021/acsami.5b10634" @default.
• W2413309827 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/26671308" @default.
• W2413309827 hasPublicationYear "2015" @default.
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