Ultrafine Dual-Phased Carbide Nanocrystals Confined in Porous Nitrogen-Doped Carbon Dodecahedrons for Efficient Hydrogen Evolution Reaction.
basic_science · Level V
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- Record sourced from PubMed, PMID 31168857.
- Also identified by DOI 10.1002/adma.201900699.
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Abstract
Designing novel non-noble electrocatalysts with controlled structures and composition remains a great challenge for efficient hydrogen evolution reaction (HER). Herein, a rational synthesis of ultrafine carbide nanocrystals confined in porous nitrogen-doped carbon dodecahedrons (PNCDs) by annealing functional zeolitic imidazolate framework (ZIF-8) with molybdate or tungstate is reported. By controlling the substitution amount of MO<sub>4</sub> units (M = Mo or W) in the ZIF-8 framework, dual-phase carbide nanocrystals confined in PNCDs (denoted as MC-M<sub>2</sub> C/PNCDs) can be obtained, which exhibit superior activity toward the HER to the single-phased MC/PNCDs and M<sub>2</sub> C/PNCDs. The evenly distributed ultrafine nanocrystals favor the exposure of active sites. PNCDs as the support facilitate charge transfer and protect the nanocrystals from aggregation during the HER process. Moreover, the strong coupling interactions between MC and M<sub>2</sub> C provide beneficial sites for both water dissociation and hydrogen desorption. This work highlights a new feasible strategy to explore efficient electrocatalysts via engineering on nanostructure and composition.