An activity lift for platinum Platinum is an excellent but expensive catalyst for the oxygen reduction reaction (ORR), which is critical for fuel cells. Alloying platinum with other metals can create shells of platinum on cores of less expensive metals, which increases its surface exposure, and compressive strain in the layer can also boost its activity (see the Perspective by Stephens et al. ). Bu et al. produced nanoplates—platinum-lead cores covered with platinum shells—that were in tensile strain. These nanoplates had high and stable ORR activity, which theory suggests arises from the strain optimizing the platinum-oxygen bond strength. Li et al. optimized both the amount of surface-exposed platinum and the specific activity. They made nanowires with a nickel oxide core and a platinum shell, annealed them to the metal alloy, and then leached out the nickel to form a rough surface. The mass activity was about double the best reported values from previous studies. Science , this issue p. 1410 , p. 1414 ; see also p. 1378

By converting ambient energy into electricity, energy harvesting is capable of at least offsetting, or even replacing, the reliance of small portable electronics on traditional power supplies, such as batteries. Here we demonstrate a novel and simple generator with extremely low cost for efficiently harvesting mechanical energy that is typically present in the form of vibrations and random displacements/deformation. Owing to the coupling of contact charging and electrostatic induction, electric generation was achieved with a cycled process of contact and separation between two polymer films. A detailed theory is developed for understanding the proposed mechanism. The instantaneous electric power density reached as high as 31.2 mW/cm(3) at a maximum open circuit voltage of 110 V. Furthermore, the generator was successfully used without electric storage as a direct power source for pulse electrodeposition (PED) of micro/nanocrystalline silver structure. The cathodic current efficiency reached up to 86.6%. Not only does this work present a new type of generator that is featured by simple fabrication, large electric output, excellent robustness, and extremely low cost, but also extends the application of energy-harvesting technology to the field of electrochemistry with further utilizations including, but not limited to, pollutant degradation, corrosion protection, and water splitting.

A hybrid-fiber nanogenerator comprising a ZnO nanowire array, PVDF polymer and two electrodes is presented. Depending on the bending or spreading action of the human arm, at an angle of ∼90°, the hybrid fiber reaches electrical outputs of ∼0.1 V and ∼10 nA cm(-2) . The unique structure of the hybrid fiber may inspire future research in wearable energy-harvesting technology.

Perovskite ferroelectric nanowires have rarely been used for the conversion of tiny mechanical vibrations into electricity, in spite of their large piezoelectricity. Here we present a lead-free NaNbO(3) nanowire-based piezoelectric device as a high output and cost-effective flexible nanogenerator. The device consists of a NaNbO(3) nanowire-poly(dimethylsiloxane) (PDMS) polymer composite and Au/Cr-coated polymer films. High-quality NaNbO(3) nanowires can be grown by hydrothermal method at low temperature and can be poled by an electric field at room temperature. The NaNbO(3) nanowire-PDMS polymer composite device shows an output voltage of 3.2 V and output current of 72 nA (current density of 16 nA/cm(2)) under a compressive strain of 0.23%. These results imply that NaNbO(3) nanowires should be quite useful for large-scale lead-free piezoelectric nanogenerator applications.

Scalable preparation of solution processable graphene and its bulk materials with high specific surface areas and designed porosities is essential for many practical applications. Herein, we report a scalable approach to produce aqueous dispersions of holey graphene oxide with abundant in-plane nanopores via a convenient mild defect-etching reaction and demonstrate that the holey graphene oxide can function as a versatile building block for the assembly of macrostructures including holey graphene hydrogels with a three-dimensional hierarchical porosity and holey graphene papers with a compact but porous layered structure. These holey graphene macrostructures exhibit significantly improved specific surface area and ion diffusion rate compared to the nonholey counterparts and can be directly used as binder-free supercapacitor electrodes with ultrahigh specific capacitances of 283 F/g and 234 F/cm(3), excellent rate capabilities, and superior cycling stabilities. Our study defines a scalable pathway to solution processable holey graphene materials and will greatly impact the applications of graphene in diverse technological areas.

Scalable growth of regular arrays of perovskite microplates opens a new platform for electronic and optoelectronic device arrays.

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