We report the chemical intercalation of Li+ into the interlayer of V2O5·nH2O with enlarged layer spacing and fast Zn2+ diffusion, resulting in high rate capability and excellent long-term cycling performance.
Exploring the interaction between two neighbouring monomers has great potential to significantly raise the performance and deepen the mechanistic understanding of heterogeneous catalysis. Herein, we demonstrate that the synergetic interaction between neighbouring Pt monomers on MoS greatly enhanced the CO hydrogenation catalytic activity and reduced the activation energy relative to isolated monomers. Neighbouring Pt monomers were achieved by increasing the Pt mass loading up to 7.5% while maintaining the atomic dispersion of Pt. Mechanistic studies reveal that neighbouring Pt monomers not only worked in synergy to vary the reaction barrier, but also underwent distinct reaction paths compared with isolated monomers. Isolated Pt monomers favour the conversion of CO into methanol without the formation of formic acid, whereas CO is hydrogenated stepwise into formic acid and methanol for neighbouring Pt monomers. The discovery of the synergetic interaction between neighbouring monomers may create a new path for manipulating catalytic properties.
High-entropy alloys (HEAs), which
are defined as near-equimolar
alloys of five or more elements, are attracting ever increasing attention
because of the unique properties in a variety of applications. Recently,
HEAs have already exhibited remarkable catalytic performance toward
several thermal-driven and electrocatalytic reactions. HEAs not only
regulate the electronic and geometric structures to a large degree
but also serve as a platform to construct catalysts with unexpected
performance. Herein, recent advances regarding HEA-based catalysis
are systematically summarized, with a special focus on the synthetic
methods for HEA-based catalysts, catalytic performance, and mechanistic
understanding. Moreover, the challenges and future opportunities for
this research area are carefully discussed. A series of open questions
and promising directions to be explored are proposed, including synthetic
methods, regulation of electronic properties, identification of active
centers, and applications into photocatalysis. This Review provides
an overview about the progress, challenges, and opportunities for
HEA-based catalysis.
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