Vertically oriented cobalt selenide/NiFe layered-double-hydroxide nanosheets supported on exfoliated graphene foil: an efficient 3D electrode for overall water splitting
Developing cost-effective electrocatalysts for both oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) in basic media is critical to renewable energy conversion technologies. Here, we report a ternary hybrid that is constructed by in situ growth of cobalt selenide (Co sub(0.85)Se)...
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Published in | Energy & environmental science Vol. 9; no. 2; pp. 478 - 483 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
01.01.2016
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Subjects | |
Online Access | Get full text |
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Summary: | Developing cost-effective electrocatalysts for both oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) in basic media is critical to renewable energy conversion technologies. Here, we report a ternary hybrid that is constructed by in situ growth of cobalt selenide (Co sub(0.85)Se) nanosheets vertically oriented on electrochemically exfoliated graphene foil, with subsequent deposition of NiFe layered-double-hydroxide by a hydrothermal treatment. The resulting 3D hierarchical hybrid, possessing a high surface area of 156 m super(2) g super(-1) and strong coupling effect, exhibits excellent catalytic activity for OER, which only requires overpotentials of 1.50 and 1.51 V to attain current densities of 150 and 250 mA cm super(-2), respectively. These overpotentials are much lower than those reported for other non-noble-metal materials and Ir/C catalysts. The hybrid also efficiently catalyzes HER in base with a current density of 10 mA cm super(-2) at an overpotential of -0.26 V. Most importantly, we achieve a current density of 20 mA cm super(-2) at 1.71 V by using the 3D hybrid as both a cathode and an anode for overall water splitting, which is well comparable to the integrated performance of Pt/C and Ir/C catalysts. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1754-5692 1754-5706 |
DOI: | 10.1039/c5ee03440j |