Metal-Organic Framework-Derived Hierarchical (Co,Ni)Se 2 @NiFe LDH Hollow Nanocages for Enhanced Oxygen Evolution
High-efficient electrocatalysts are crucial for fuel cell applications; however, the whole cell performance is generally restricted by the anodic part because of the sluggish kinetics involved in the oxygen evolution reaction (OER) process. Herein, a hierarchical hollow (Co,Ni)Se @NiFe layered doubl...
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Published in | ACS applied materials & interfaces Vol. 11; no. 8; pp. 8106 - 8114 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
27.02.2019
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Subjects | |
Online Access | Get full text |
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Summary: | High-efficient electrocatalysts are crucial for fuel cell applications; however, the whole cell performance is generally restricted by the anodic part because of the sluggish kinetics involved in the oxygen evolution reaction (OER) process. Herein, a hierarchical hollow (Co,Ni)Se
@NiFe layered double hydroxide (LDH) nanocage was synthesized by deriving from the metal-organic framework (MOF) of ZIF-67. Concretely, it involves first fabrication of hollow rhombic (Co,Ni)Se
nanocages and then deposition of NiFe LDH nanosheets on the surface of nanocages. Notably, the incorporation of Ni into Co-based ZIF-67 (via ion-exchange) could tail the atomic arrangement of the MOF, exposing more additional active sites in the following selenization treatment. The as-synthesized (Co,Ni)Se
@NiFe LDH demonstrates splendid OER performance with a small overpotential of 277 mV (to launch a current density of 10 mA cm
), a small Tafel slope of 75 mV dec
, and robust durability (a slight stability decay of 5.1% after 17 h of continuous test), not only surpassing the commercial RuO
but also being comparable/superior to most reported nonprevious metal-based catalysts. Upon analysis, the outstanding OER performance is attributed to the optimized adsorption/desorption nature of iron and nickel/cobalt toward the oxygenated species and partial delocalization of spin status at the interface via the bridging O
. This work represents a solid step toward exploration of advanced catalysts with deliberate experimental design and/or atom tailoring. |
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ISSN: | 1944-8244 1944-8252 |
DOI: | 10.1021/acsami.8b22133 |