Interfacial Engineering of Bimetallic Ni/Co-MOFs with H-Substituted Graphdiyne for Ammonia Electrosynthesis from Nitrate.
basic_science · Level V
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- Record sourced from PubMed, PMID 36930780.
- Also identified by DOI 10.1021/acsnano.2c12491.
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Abstract
The electrochemical synthesis of ammonia is highly dependent on the coupling reaction between nitrate and water, for which an electrocatalyst with a multifunctional interface is anticipated to promote the deoxygenation and hydrogenation of nitrate with water. Herein, by engineering the surface of bimetallic Ni/Co-MOFs (NiCoBDC) with hydrogen-substituted graphdiyne (HsGDY), a hybrid nanoarray of NiCoBDC@HsGDY with a multifunctional interface has been achieved toward scale-up of the nitrate-to-ammonia conversion. On the one hand, a partial electron transfers from Ni<sup>2+</sup> to the coordinatively unsaturated Co<sup>2+</sup> on the surface of NiCoBDC, which not only promotes the deoxygenation of *NO<sub>3</sub> on Co<sup>2+</sup> but also activates the water-dissociation to *H on Ni<sup>2+</sup>. On the other hand, the conformal coated HsGDY facilitates both electrons and NO<sub>3</sub><sup>-</sup> ions gathering on the interface between NiCoBDC and HsGDY, which moves forward the rate-determining step from the deoxygenation of *NO<sub>3</sub> to the hydrogenation of *N with both *H on Ni<sup>2+</sup> and *H<sub>2</sub>O on Co<sup>2+</sup>. As a result, such a NiCoBDC@HsGDY nanoarray delivers high NH<sub>3</sub> yield rates with Faradaic efficiency above 90% over both wide potential and pH windows. When assembled into a galvanic Zn-NO<sub>3</sub><sup>-</sup> battery, a power density of 3.66 mW cm<sup>-2</sup> is achieved, suggesting its potential in the area of aqueous Zn-based batteries.