2 research outputs found
Structure Effects of 2D Materials on α‑Nickel Hydroxide for Oxygen Evolution Reaction
To
engineer low-cost, high-efficiency, and stable oxygen evolution
reaction (OER) catalysts, structure effects should be primarily understood.
Focusing on this, we systematically investigated the relationship
between structures of materials and their OER performances by taking
four 2D α-NiÂ(OH)<sub>2</sub> as model materials, including layer-stacked
bud-like NiÂ(OH)<sub>2</sub>-NB, flower-like NiÂ(OH)<sub>2</sub>-NF,
and petal-like NiÂ(OH)<sub>2</sub>-NP as well as the ultralarge sheet-like
NiÂ(OH)<sub>2</sub>-NS. For the first three (layer-stacking) catalysts,
with the decrease of stacked layers, their accessible surface areas,
abilities to adsorb OH<sup>–</sup>, diffusion properties, and
the intrinsic activities of active sites increase, which accounts
for their steadily enhanced activity. As expected, NiÂ(OH)<sub>2</sub>-NP shows the lowest overpotential (260 mV at 10 mA cm<sup>–2</sup>) and Tafel slope (78.6 mV dec<sup>–1</sup>) with a robust
stability over 10 h among the samples, which also outperforms the
benchmark IrO<sub>2</sub> (360 mV and 115.8 mV dec<sup>–1</sup>) catalyst. Interestingly, NiÂ(OH)<sub>2</sub>-NS relative to NiÂ(OH)<sub>2</sub>-NP exhibits even faster substance diffusion due to the sheet-like
structure, but shows inferior OER activity, which is mainly because
the NiÂ(OH)<sub>2</sub>-NP with a smaller size possesses more active
boundary sites (higher reactivity of active sites) than NiÂ(OH)<sub>2</sub>-NS, considering the adsorption properties and accessible
surface areas of the two samples are quite similar. By comparing the
different structures and their OER behaviors of four α-NiÂ(OH)<sub>2</sub> samples, our work may shed some light on the structure effect
of 2D materials and accelerate the development of efficient OER catalysts
In Situ Synthesis of Core–Shell Pt–Cu Frame@Metal–Organic Frameworks as Multifunctional Catalysts for Hydrogenation Reaction
Controllable integration
of metal nanoparticles (NPs) and metal–organic
frameworks (MOFs) is of significant importance in many applications
owing to their unique properties. In situ efficient synthesis of metal
NPs with different structures into MOFs is a great challenge. Herein,
we report the nanostructures of octahedron and flower Pt–Cu
frame@HKUST-1, which is successfully synthesized under a microwave
irradiation method in only 30 min. In this study, Pt–Cu alloys,
serving as the self-template, are synthesized first, followed by the
HKUST-1 shell growing in situ via the consumption of Cu<sup>0</sup>. As multifunctional catalysts, the core–shell structures
exhibit excellent performance for the hydrogenation of 1-hexene. Notably,
octahedron Pt–Cu frame@HKUST-1 displays high turnover number
(TON) and turnover frequency (TOF) of 1004 and 2008 h<sup>–1</sup>, respectively. Thanks to
the protective effect of HKUST-1, the octahedron Pt–Cu frame@HKUST-1
can be recycled for at least four runs without serious loss of activity
and obvious aggregation of Pt–Cu alloys. Furthermore, the size-selective
catalysis is also well-demonstrated by choosing 1-hexene, <i>cis</i>-cyclooctene, and styrene as substrates