Issue 47, 2018

Energy-efficient 1.67 V single- and 0.90 V dual-electrolyte based overall water-electrolysis devices enabled by a ZIF-L derived acid–base bifunctional cobalt phosphide nanoarray

Abstract

Zeolitic imidazolate frameworks (ZIFs) have been widely utilized as templates to construct hollow or porous nanostructures with superior catalytic properties for various electrocatalytic reactions. In this work, we reported that a leaf-like cobalt phosphide nanoarray topology assembled on carbon cloth (CoP NS/CC) built through annealing followed by phosphorization of the template precursor of the ZIF-L-Co nanosheet array on CC could serve as an efficient versatile catalyst for water electrolysis. This CoP NS/CC exhibits satisfactory HER, OER and full water-splitting efficiencies, with overpotentials of 90 mV and 310 mV and a voltage of 1.67 V needed to afford a current density of 10 mA cm−2, respectively. Also, this electrode shows an excellent and stable HER performance in 0.5 M H2SO4 with a low overpotential of 88.7 mV required to attain a current density of 10 mA cm−2. In this regard, a novel acid|base hybrid overall water-splitting electrolyzer with this CoP NS/CC serving as both the anode and cathode was further built, wherein cell voltages of just 0.735 (onset voltage) and 0.9 V were needed to afford overall current densities of 1 and 10 mA cm−2, respectively.

Graphical abstract: Energy-efficient 1.67 V single- and 0.90 V dual-electrolyte based overall water-electrolysis devices enabled by a ZIF-L derived acid–base bifunctional cobalt phosphide nanoarray

Supplementary files

Article information

Article type
Paper
Submitted
04 Sep 2018
Accepted
09 Nov 2018
First published
12 Nov 2018

J. Mater. Chem. A, 2018,6, 24277-24284

Energy-efficient 1.67 V single- and 0.90 V dual-electrolyte based overall water-electrolysis devices enabled by a ZIF-L derived acid–base bifunctional cobalt phosphide nanoarray

W. Zhu, W. Zhang, Y. Li, Z. Yue, M. Ren, Y. Zhang, N. M. Saleh and J. Wang, J. Mater. Chem. A, 2018, 6, 24277 DOI: 10.1039/C8TA08577C

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