A novel Co-based MOF/Pd composite: synergy of charge-transfer towards the electrocatalytic oxygen evolution reaction
A novel Co-based MOF/Pd composite (LEEL-037/Pd-C) was synthesized and evaluated towards the oxygen evolution reaction (OER) in alkaline medium. The composites' formation improved the surface-electrochemistry of Pd nanoparticles to carry out the OER. XRD and TEM reveal a crystallite size increas...
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Veröffentlicht in: | CrystEngComm 2021-04, Vol.23 (16), p.2982-2991 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | A novel Co-based MOF/Pd composite (LEEL-037/Pd-C) was synthesized and evaluated towards the oxygen evolution reaction (OER) in alkaline medium. The composites' formation improved the surface-electrochemistry of Pd nanoparticles to carry out the OER. XRD and TEM reveal a crystallite size increase and a crystal lattice distortion for LEEL-037/Pd-C composites. LEEL-037/Pd-C samples containing 25 and 50 wt% LEEL-037 show an improvement of the electrochemical surface area (ECSA) due to a structural interaction that enhances the electrocatalytic activity of bare materials. Based on the electrochemical and XPS results, a charge-transfer mechanism is proposed to explain an improvement of the OH
−
adsorption degree on the LEEL-037/Pd-C composites. Since OER activity in alkaline medium is directly related to the initial OH
−
adsorption process, LEEL-037/Pd-C composites enhance their OER electrocatalytic activity. The composite LEEL-037(25)/Pd-C(75) exhibited the lowest operational potential to reach 10 mA cm
−2
(1.66 V); additionally, the EIS measurements show that it exhibited the lowest charge-transfer resistance. Insights into this reaction mechanism and charge-transfer process become a promising strategy to tailor the electrochemical activity towards the OER.
A novel Co-based MOF/Pd composite (LEEL-037/Pd-C) presented an electronic transference (Co 3d orbital → linkers π* → Pd 5S orbital) promoting an enhanced OH
−
adsorption, thus improving the oxygen evolution reaction (OER) in alkaline medium. |
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ISSN: | 1466-8033 1466-8033 |
DOI: | 10.1039/d0ce01747g |