Potentiodynamic deposition of composition influenced Co1−xNix LDHs thin film electrode for redox supercapacitors
Current paper comprises the electrodeposition of nanostructured porous Co1−xNix layered double hydroxide (Co1−xNix LDHs) thin films on to stainless steel substrate by a potentiodynamic mode. The compositional impacts on the various properties of Co1−xNix LDHs are examined via structural, morphologic...
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Veröffentlicht in: | International journal of hydrogen energy 2013-04, Vol.38 (10), p.4046-4053 |
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Sprache: | eng |
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Zusammenfassung: | Current paper comprises the electrodeposition of nanostructured porous Co1−xNix layered double hydroxide (Co1−xNix LDHs) thin films on to stainless steel substrate by a potentiodynamic mode. The compositional impacts on the various properties of Co1−xNix LDHs are examined via structural, morphological, surface wettability and electrochemical studies. The nanocrystalline Co1−xNix LDHs thin films possess varying porous, nanoflake like morphology and superhydrophilic behavior by the composition influence. Electrochemical studies demonstrate the supercapacitive performance of Co1−xNix LDHs thin film electrodes. The maximal specific capacitance for Co1−xNix LDHs electrode is found to be ∼1213 F g−1 for composition Co0.66Ni0.34 LDH in 2 M KOH electrolyte at 5 mV s−1 scan rate owing specific energy of 104 Whkg−1, specific power of 1.44 kW kg−1 with ∼94% of coulomb efficiency and stability of electrode retained to 77% after 10,000th cycle. The high capacitance retention proposes the deposited Co1−xNix LDHs thin film as promising contender for supercapacitor applications.
► Co1−xNix layered double hydroxides by potentiodynamical mode. ► The Co1−xNix LDHs thin film electrodes as redox supercapacitor with specific capacitance ∼ 1213 F g−1. ► Highly electrochemical cyclic stability retained 77% after 10,000th cycle. ► Co0.66Ni0.34 LDHs showed specific energy = 104 W h kg−1, specific power = 1.44 kW kg−1 and coulomb efficiency ∼94%. |
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ISSN: | 0360-3199 1879-3487 |
DOI: | 10.1016/j.ijhydene.2013.01.047 |