4.6 Article

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

Journal

JOURNAL OF MATERIALS CHEMISTRY A
Volume 6, Issue 19, Pages 9009-9018

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c8ta02528b

Keywords

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Funding

  1. National Natural Science Foundation of China [21561012, 51772213, 11174219, 11474217]
  2. Ministry of Education, Singapore [MOE2015-T2-2-094]
  3. Natural Science Foundation of Shanghai [18ZR1442300]
  4. Basic Scientific Research Funds of Central Universities

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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 H2SO4, 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.

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