Selective and durable HO electrosynthesis catalyst in acid by selenization induced straining and phasing.

Developing efficient electrocatalysts for acidic electrosynthesis of hydrogen peroxide (HO) holds considerable significance, while the selectivity and stability of most materials are compromised under acidic conditions. Herein, we demonstrate that constructing amorphous platinum-selenium (Pt-Se) shells on crystalline Pt cores can manipulate the oxygen reduction reaction (ORR) pathway to efficiently catalyze the electrosynthesis of HO in acids. The Se‒Pt nanoparticles, with optimized shell thickness, exhibit over 95% selectivity for HO production, while suppressing its decomposition.

Synthesis of amorphous trimetallic PdCuNiP nanoparticles for enhanced OER.

Metal phosphides with multi-element components and amorphous structure represent a novel kind of electrocatalysts for promising activity and durability towards the oxygen evolution reaction (OER). In this work, a two-step strategy, including alloying and phosphating processes, is reported to synthesize trimetallic amorphous PdCuNiP phosphide nanoparticles for efficient OER under alkaline conditions. The synergistic effect between Pd, Cu, Ni, and P elements, as well as the amorphous structure of the obtained PdCuNiP phosphide nanoparticles, would boost the intrinsic catalytic activity of Pd nanoparticles towards a wide range of reactions.

Tailoring Amorphous PdCu Nanostructures for Efficient C-C Cleavage in Ethanol Electrooxidation.

The large-scale application of direct ethanol fuel cells has long been obstructed by the sluggish ethanol oxidation reaction at the anode. Current wisdom for designing and fabricating EOR electrocatalysts has been focused on crystalline materials, which result in only limited improvement in catalytic efficiency. Here, we report the amorphous PdCu (a-PdCu) nanomaterials as superior EOR electrocatalysts.

Mastering the surface strain of platinum catalysts for efficient electrocatalysis.

Platinum (Pt) has found wide use as an electrocatalyst for sustainable energy conversion systems. The activity of Pt is controlled by its electronic structure (typically, the d-band centre), which depends sensitively on lattice strain. This dependence can be exploited for catalyst design, and the use of core-shell structures and elastic substrates has resulted in strain-engineered Pt catalysts with drastically improved electrocatalytic performances.

General Synthesis of Amorphous PdM (M = Cu, Fe, Co, Ni) Alloy Nanowires for Boosting HCOOH Dehydrogenation.

Noble metal-based nanomaterials with amorphous structures are promising candidates for developing efficient electrocatalysts. However, their synthesis remains a significant challenge, especially under mild conditions. In this paper, we report a general strategy for preparing amorphous PdM nanowires (a-PdM NWs, M = Fe, Co, Ni, and Cu) at low temperatures by exploiting glassy non-noble metal (M) nuclei generated by special ligand adsorption as the amorphization dictator.

Deposition of Atomically Thin Pt Shells on Amorphous Palladium Phosphide Cores for Enhancing the Electrocatalytic Durability.

As an excellent electrocatalyst, platinum (Pt) is often deposited as a thin layer on a nanoscale substrate to achieve high utilization efficiency. However, the practical application of the as-designed catalysts has been substantially restricted by the poor durability arising from the leaching of cores. Herein, by employing amorphous palladium phosphide (a-Pd-P) as substrates, we develop a class of leaching-free, ultrastable core-shell Pt catalysts with well-controlled shell thicknesses and surface structures for fuel cell electrocatalysis.

Engineering Surface Structure of Pt Nanoshells on Pd Nanocubes to Preferentially Expose Active Surfaces for ORR by Manipulating the Growth Kinetics.

Synthesis of Pt nanoshells on substrates can increase the utilization efficiency of Pt atoms and reduce the amount of Pt used in the applications. However, it is still an enormous challenge in tailoring the required crystal facets of Pt nanoshells on a given substrate. In this work, we demonstrate a facile and convenient approach capable for generating Pt octahedral islands with tunable sizes and densities on Pd nanocubes by manipulating the deposition rate.

Inflating hollow nanocrystals through a repeated Kirkendall cavitation process.

The Kirkendall effect has been recently used to produce hollow nanostructures by taking advantage of the different diffusion rates of species involved in the chemical transformations of nanoscale objects. Here we demonstrate a nanoscale Kirkendall cavitation process that can transform solid palladium nanocrystals into hollow palladium nanocrystals through insertion and extraction of phosphorus. The key to success in producing monometallic hollow nanocrystals is the effective extraction of phosphorus through an oxidation reaction, which promotes the outward diffusion of phosphorus from the compound nanocrystals of palladium phosphide and consequently the inward diffusion of vacancies and their coalescence into larger voids.

Synthesis of Pd Nanoframes by Excavating Solid Nanocrystals for Enhanced Catalytic Properties.

Synthesis of metal nanoframes has been of great interest for their open structures and high fractions of active surface sites, which gives rise to outstanding performance in catalysis. In this work, Pd nanoframes with well-defined structures have been successfully prepared by directly excavating solid nanocrystals. The success of this synthesis mainly relies on the fine control over the oxidative etching and regrowth rates.