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Metal-organic framework-derived integrated nanoarrays for overall water splitting

Earth-abundant electrocatalysts for both the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) in a wide pH range are highly desirable for sustainable energy conversion technologies, but challenging to develop. Herein, we report hollow CoP nanosphere-embedded carbon nanotube/nitr...

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Published in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2018, Vol.6 (19), p.99-918
Main Authors: Guan, Cao, Wu, Haijun, Ren, Weina, Yang, Chunhai, Liu, Ximeng, Ouyang, Xiaofang, Song, Zeyi, Zhang, Yuzhong, Pennycook, Stephen J, Cheng, Chuanwei, Wang, John
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Language:English
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Summary:Earth-abundant electrocatalysts for both the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) in a wide pH range are highly desirable for sustainable energy conversion technologies, but challenging to develop. Herein, we report hollow CoP nanosphere-embedded carbon nanotube/nitrogen-doped carbon (NC-CNT/CoP) nanoarrays, in which a nanoscale Kirkendall effect generates few-layer graphene-coated hollow CoP nanospheres with abundant active sites. The integrated NC-CNT/CoP electrode behaves as an efficient pH-universal HER catalyst and, through in situ transformation, the derived materials show excellent OER performance. The NC-CNT/CoP-based electrolyzers achieve a current density of 10 mA cm −2 at low voltages of 1.63, 1.69, and 1.66 V in KOH, PBS, and H 2 SO 4 , respectively, which are similar to the values obtained using noble metal catalysts. Importantly, the integrated electrode exhibits superior stability than that of the benchmark noble metals in a wide pH range. This work presents a promising method for achieving nonprecious catalysts for efficient energy conversion. A unique integrated hollow CoP nanospheres embedded carbon nanoarrays has been facilely synthesized from a metal-organic framework precursor, and behaves as a pH-versatile catalyst for both hydrogen evolution and oxygen evolution reactions.
ISSN:2050-7488
2050-7496
DOI:10.1039/c8ta02528b