Crystalline core-amorphous shell heterostructures: epitaxial assembly of NiB nanosheets onto PtPd mesoporous hollow nanopolyhedra for enhanced hydrogen evolution electrocatalysis

Engineering the composition and structure of hybrid electrocatalysts based on precious Pt and non-precious metals is of paramount importance for increasing the utilization efficiency of Pt and enhancing their electrocatalytic performance. Here we report the construction of novel crystalline PtPd @ a...

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Veröffentlicht in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2020-01, Vol.8 (18), p.8927-8933
Hauptverfasser: Deng, Kai, Ren, Tianlun, Xu, You, Liu, Songliang, Dai, Zechuan, Wang, Ziqiang, Li, Xiaonian, Wang, Liang, Wang, Hongjing
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Sprache:eng
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Zusammenfassung:Engineering the composition and structure of hybrid electrocatalysts based on precious Pt and non-precious metals is of paramount importance for increasing the utilization efficiency of Pt and enhancing their electrocatalytic performance. Here we report the construction of novel crystalline PtPd @ amorphous NiB core-shell heterostructures (c-PtPd@a-NiB CSHs) with crystalline PtPd mesoporous truncated octahedral nanocages (c-PtPd MTONs) as the cores and amorphous NiB (a-NiB) nanosheets as the shells via a three-step strategy. This hybridization, between c-PtPd MTONs and a-NiB nanosheets, leads to increased catalytically active sites, a modulated surface electronic structure, and enhanced hydrophilic properties. With these properties, the as-obtained c-PtPd@a-NiB CSHs exhibit enhanced electrocatalytic activity toward the hydrogen evolution reaction (HER) in an alkaline medium, with a small required overpotential of 31 mV (@-10 mA cm −2 ), a low Tafel slope of 40.9 mV dec −1 , and excellent long-term catalytic durability. Crystalline core-amorphous shell heterostructures composed of PtPd mesoporous hollow nanopolyhedra and NiB nanosheets exhibit enhanced electrocatalytic performance toward the hydrogen evolution reaction.
ISSN:2050-7488
2050-7496
DOI:10.1039/d0ta02537b