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Multi-component nanoporous platinum–ruthenium–copper–osmium–iridium (np-PtRuCuOsIr) electrocatalyst has been facilely fabricated by chemical dealloying of mechanically alloyed AlCuPtRuOsIr precursor. The np-PtRuCuOsIr catalyst exhibits a typical three-dimensional bi-continuous interpenetrating ligament/channel structure with a length scale of ∼2.5 nm. The np-PtRuCuOsIr catalyst reaches a higher level in the mass activity (857.5 mA mg Pt −1 ) and specific activity (3.0 mA cm −2 ) towards methanol oxidation compared to the commercial PtC catalyst (229.5 mA mg Pt −1 and 0.5 mA cm −2 respectively). Moreover, the CO stripping peak of np-PtRuCuOsIr is 0.54 V (vs. SCE), 130 mV negative shift in comparison with the commercial PtC (0.67 V vs. SCE). The half-wave potential of np-PtRuCuOsIr is 0.900 V vs. RHE, 36 mV positive compared with that of the commercial PtC (0.864 V vs. RHE). The np-PtRuCuOsIr catalyst also shows 1.8 and 3.8 times enhancement in the mass and specific activity towards oxygen reduction than the commercial PtC. Moreover, the np-PtRuCuOsIr alloy exhibits superior oxygen reduction activities even after 15 K cycles, indicating its excellent long-term stability. The present np-PtRuCuOsIr can act as a promising candidate for the electrocatalyst in direct methanol fuel cells (DMFCs). [ABSTRACT FROM AUTHOR]

Metallic actuators have attracted a great deal of attention owing to their potential advantages over piezoelectric ceramics and conducting polymers. Here, we report different electrochemical actuation behaviors of bulk nanoporous palladium (np-Pd) fabricated by dealloying in acid (0.5 M H 2 SO 4 ) and alkaline (1.0 M KOH) solutions. In the 1.0 M KOH solution, the reversible expansion/contraction of np-Pd well responds to the adsorption/desorption of involved species (H and OH). In the 0.5 M H 2 SO 4 solution, only continuous contraction can be observed in the potential region involving the H-adsorption/desorption, but the reversible strain appears in the potential region related to the OH-adsorption/desorption. Moreover, the surface stress-charge coefficient (ξ) exhibits inverse signs associated with the H-adsorption (absorption)/desorption and OH-adsorption/desorption in the alkaline solution. More importantly, the reversible strain amplitude of np-Pd can be regulated by changing the potential scan rate or by being stimulated in different electrolytes. [ABSTRACT FROM AUTHOR]

The electrochemically induced electrical resistance response of nanostructured metallic materials is an important issue in interdisciplinary fields including electrochemistry, physics and surface science. Nanoporous metals possess an open three-dimensional bicontinuous ligament (nanowire network)-channel (nanopore) structure with high surface-to-volume ratios, and show great potentials for investigations in this topic. Here we fabricate nanoporous silver (NPS) with high density of lattice defects (dislocations, twins, stacking defaults and grain boundaries) and ligaments composed of Ag nanocrystals with sizes comparable to the ligament length scale. More importantly, the present NPS shows extraordinarily enhanced reversible resistance response to electrochemical stimuli in alkaline electrolytes. A giant reversible resistance change of up to ∼1100% has been achieved in NPS. Moreover, the reversible electrical resistance change of NPS can be well modulated through cyclic voltammetry or square wave potential input. The related mechanisms have been rationalized on the basis of reversible oxide formation/reduction on the ligament surface of NPS, silver dissolution, as well as the effects of lattice defects in NPS. [ABSTRACT FROM AUTHOR]

Nanoporous tungsten (np-W) synthesized by a facile dealloying strategy was utilized as the host to accommodate tellurium (Te) for Li-Te batteries. The np-W supported Te (np-W-Te) cathode exhibits an excellent specific volumetric capacity of 1168 mA h cm−3 after 30 cycles, a good cycling performance of 200 cycles with a coulombic efficiency over 98.9%, and fast rate capabilities of 1612 mA h cm−3 at a current density of 50 mA g−1 and 774 mA h cm−3 at 800 mA g−1. The excellent performance of the np-W-Te cathode is attributed to the highly dispersed Te impregnated in the np-W host with rich porosity, high conductivity and superior stability. The mechanism investigation by in situ Raman and ex situ XRD techniques demonstrates the reversible transformation between Li and Li 2 Te during the charge/discharge processes. This study highlights the nanoporous metal as a promising host to confine Te for Li-Te batteries. Nanoporous tungsten synthesized by dealloying acted as the host to accommodate Te for Li-Te batteries. ga1 • The as-dealloyed nanoporous W hosted Te as the cathode for Li-Te batteries. • The cathode exhibited high specific capacity, good cycling and rate performances. • The reversible conversion between Te and Li 2 Te is the mechanism for the battery. [ABSTRACT FROM AUTHOR]