A nanoporous PdNi (NP-PdNi) alloy with uniform structure dimension is easily fabricated by one-step mild dealloying of a PdNiAl precursor alloy. NP-PdNi consists of an interconnected nanoscaled network backbone and bicontinuous hollow channels in all three dimensions with a typical ligament size of around 5 nm. Electrochemical measurements indicated that the NP-PdNi alloy has superior electrocatalytic activity towards oxygen reduction reaction (ORR) with much higher specific and mass activities as well as higher methanol tolerance compared with Pt/C catalysts. Importantly, NP-PdNi suffers less loss of the ORR activity and the electrochemical surface area of metal upon 5000 potential cycles in acid solution than Pt/C, indicating a better catalytic durability. The NP-PdNi alloy holds great application potential as a cathode electrocatalyst in the fuel cell related technology with unique ORR performance, high structure stability, and easy preparation.
Supported Pd catalysts are active in catalyzing the highly exothermic methane combustion reaction but tend to be deactivated owing to local hyperthermal environments. Herein we report an effective approach to stabilize Pd/SiO2 catalysts with porous Al2O3 overlayers coated by atomic layer deposition (ALD). 27Al magic angle spinning NMR analysis showed that Al2O3 overlayers on Pd particles coated by the ALD method are rich in pentacoordinated Al3+ sites capable of strongly interacting with adjacent surface PdOx phases on supported Pd particles. Consequently, Al2O3‐decorated Pd/SiO2 catalysts exhibit active and stable PdOx and Pd–PdOx structures to efficiently catalyze methane combustion between 200 and 850 °C. These results reveal the unique structural characteristics of Al2O3 overlayers on metal surfaces coated by the ALD method and provide a practical strategy to explore stable and efficient supported Pd catalysts for methane combustion.
Nanoporous (NP) PdPt alloy with uniform ligament size and controllable bimetallic ratio is easily fabricated through the selective dealloying of Al from PdPtAl ternary alloys. Compared with commercial Pd/C, Pt/C, NP-Pd, and NP-Pt catalysts, the as-prepared NP-PdPt exhibits greatly enhanced electrocatalytic activity for formic acid oxidation. Moreover, NP-PdPt presents superior catalytic durability upon alloying with Pt, with less loss of the formic acid oxidation activity upon long term potential scans. The NP-PdPt alloy holds great potential in applications as a promising anode catalyst in direct formic acid fuel cells.
A one-step dealloying method is employed to conveniently fabricate a bimodal porous (BP) Si/Ag composite in high throughput under mild conditions. Upon dealloying the carefully designed SiAgAl ternary alloy in HCl solution at room temperature, the obtained Si/Ag composite has a uniform bicontinuous porous structure in three dimensions with micro-nano bimodal pore size distribution. Compared with the traditional preparation methods for porous Si and Si-based composites, this dealloying route is easily operated and environmentally benign. More importantly, it is convenient to realize the controllable components and uniform distribution of Si and Ag in the product. Owing to the rich porosity of the unique BP structure and the incorporation of highly conductive Ag, the as-made Si/Ag composite possesses the improved conductivity and alleviated volume changes of the Si network during repeated charging and discharging. As expected, the BP Si/Ag anode exhibits high capacity, excellent cycling reversibility, long cycling life and good rate capability for lithium storage. When the current rate is up to 1 A g(-1), BP Si/Ag can deliver a stable reversible capacity above 1000 mA h g(-1), and exhibits a capacity retention of up to 89.2% against the highest capacity after 200 cycles. With the advantages of unique performance and easy preparation, the BP Si/Ag composite holds great application potential as an advanced anode material for Li-ion batteries.
Upon dealloying a carefully designed CoCuAl ternary alloy in NaOH solution at room temperature, a Co3 O4 /CuO nanocomposite with an interconnected porous microstructure assembled by a secondary structure of nanosheets was successfully fabricated. By using the dealloying strategy, the target metals directly grew to form uniform bimetallic oxide nanocomposites. Owing to the unique hierarchical structure and the synergistic effect of both active electrode materials, the Co3 O4 /CuO nanocomposite exhibits much enhanced electrochemical performance with higher capacities and better cycling stability compared to anodes of pure Co3 O4 . Moreover, it performs excellently in terms of cycle reversibility, Coulombic efficiency, and rate capability, at both low or high current rates. With the advantages of unique performance and ease of preparation, the as-made Co3 O4 /CuO nanocomposite demonstrates promising application potential as an advanced anode material for lithium-ion batteries.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.