An important trend in electronics involves the development of materials, mechanical designs and manufacturing strategies that enable the use of unconventional substrates, such as polymer films, metal foils, paper sheets or rubber slabs. The last possibility is particularly challenging because the systems must accommodate not only bending but also stretching. Although several approaches are available for the electronics, a persistent difficulty is in power supplies that have similar mechanical properties, to allow their co-integration with the electronics. Here we introduce a set of materials and design concepts for a rechargeable lithium ion battery technology that exploits thin, low modulus silicone elastomers as substrates, with a segmented design in the active materials, and unusual 'self-similar' interconnect structures between them. The result enables reversible levels of stretchability up to 300%, while maintaining capacity densities of B1.1 mAh cm À 2 . Stretchable wireless power transmission systems provide the means to charge these types of batteries, without direct physical contact.

Rapid charge and discharge rates have become an important feature of electrical energy storage devices, but cause dramatic reductions in the energy that can be stored or delivered by most rechargeable batteries (their energy capacity). Supercapacitors do not suffer from this problem, but are restricted to much lower stored energy per mass (energy density) than batteries. A storage technology that combines the rate performance of supercapacitors with the energy density of batteries would significantly advance portable and distributed power technology. Here, we demonstrate very large battery charge and discharge rates with minimal capacity loss by using cathodes made from a self-assembled three-dimensional bicontinuous nanoarchitecture consisting of an electrolytically active material sandwiched between rapid ion and electron transport pathways. Rates of up to 400C and 1,000C for lithium-ion and nickel-metal hydride chemistries, respectively, are achieved (where a 1C rate represents a one-hour complete charge or discharge), enabling fabrication of a lithium-ion battery that can be 90% charged in 2 minutes.

High-performance miniature power sources could enable new microelectronic systems. Here we report lithium ion microbatteries having power densities up to 7.4 mW cm À 2 mm À 1 , which equals or exceeds that of the best supercapacitors, and which is 2,000 times higher than that of other microbatteries. Our key insight is that the battery microarchitecture can concurrently optimize ion and electron transport for high-power delivery, realized here as a three-dimensional bicontinuous interdigitated microelectrodes. The battery microarchitecture affords trade-offs between power and energy density that result in a high-performance power source, and which is scalable to larger areas.

Hierarchical assembly of hollow microstructures is of great scientific and practical value and remains a great challenge. This paper presents a facile and one‐pot synthesis of Cu2O microspheres with multilayered and porous shells, which were organized by nanocrystals. The time‐dependent experiments revealed a two‐step organization process, in which hollow microspheres of Cu2(OH)3NO3 were formed first due to the Ostwald ripening and then reduced by glutamic acid, the resultant Cu2O nanocrystals were deposited on the hollow intermediate microspheres and organized into finally multishell structures. The special microstructures actually recorded the evolution process of materials morphologies and microstructures in space and time scales, implying an intermediate‐templating route, which is important for understanding and fabricating complex architectures. The Cu2O microspheres obtained were used to fabricate a gas sensor, which showed much higher sensitivity than solid Cu2O microspheres.

Lithium metal anodes hold great promise to enable high-energy battery systems. However, lithium dendrites at the interface between anode and separator pose risks of short circuits and fire, impeding the safe application. In contrast to conventional approaches of suppressing dendrites, here we show a deposition-regulating strategy by electrically passivating the top of a porous nickel scaffold and chemically activating the bottom of the scaffold to form conductivity/lithiophilicity gradients, whereby lithium is guided to deposit preferentially at the bottom of the anode, safely away from the separator. The resulting lithium anodes significantly reduce the probability of dendrite-induced short circuits. Crucially, excellent properties are also demonstrated at extremely high capacity (up to 40 mAh cm −2 ), high current density, and/or low temperatures (down to −15 °C), which readily induce dendrite shorts in particular. This facile and viable deposition-regulating strategy provides an approach to preferentially deposit lithium in safer positions, enabling a promising anode for next-generation lithium batteries.

Silicon-based lithium ion battery anodes are attracting significant attention because of silicon's exceptionally high lithium capacity. However, silicon's large volume change during cycling generally leads to anode pulverization unless the silicon is dispersed throughout a matrix in nanoparticulate form. Because pulverization results in a loss of electric connectivity, the reversible capacity of most silicon anodes dramatically decays within a few cycles. Here we report a three-dimensional (3D) bicontinuous silicon anode formed by depositing a layer of silicon on the surface of a colloidal crystal templated porous nickel metal scaffold, which maintains electrical connectivity during cycling due to the scaffold. The porous metal framework serves to both impart electrical conductivity to the anode and accommodate the large volume change of silicon upon lithiation and delithiation. The initial capacity of the bicontinuous silicon anode is 3568 (silicon basis) and 1450 mAh g(-1) (including the metal framework) at 0.05C. After 100 cycles at 0.3C, 85% of the capacity remains. Compared to a foil-supported silicon film, the 3D bicontinuous silicon anode exhibits significantly improved mechanical stability and cycleability.

Hydrogen production is the key step for the future hydrogen economy. As a promising H production route, electrolysis of water suffers from high overpotentials and high energy consumption. This study proposes an N-doped CoP as the novel and effective electrocatalyst for hydrogen evolution reaction (HER) and constructs a coupled system for simultaneous hydrogen and sulfur production. Nitrogen doping lowers the d-band of CoP and weakens the H adsorption on the surface of CoP because of the strong electronegativity of nitrogen as compared to phosphorus. The H adsorption that is close to thermos-neutral states enables the effective electrolysis of the HER. Only -42 mV is required to drive a current density of -10 mA cm for the HER. The oxygen evolution reaction in the anode is replaced by the oxidation reaction of Fe , which is regenerated by a coupled H S absorption reaction. The coupled system can significantly reduce the energy consumption of the HER and recover useful sulfur sources.

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