We report on the development of highly conductive NiCo2S4 single crystalline nanotube arrays grown on a flexible carbon fiber paper (CFP), which can serve not only as a good pseudocapacitive material but also as a three-dimensional (3D) conductive scaffold for loading additional electroactive materials. The resulting pseudocapacitive electrode is found to be superior to that based on the sibling NiCo2O4 nanorod arrays, which are currently used in supercapacitor research due to the much higher electrical conductivity of NiCo2S4. A series of electroactive metal oxide materials, including CoxNi1-x(OH)2, MnO2, and FeOOH, were deposited on the NiCo2S4 nanotube arrays by facile electrodeposition and their pseudocapacitive properties were explored. Remarkably, the as-formed CoxNi1-x(OH)2/NiCo2S4 nanotube array electrodes showed the highest discharge areal capacitance (2.86 F cm(-2) at 4 mA cm(-2)), good rate capability (still 2.41 F cm(-2) at 20 mA cm(-2)), and excellent cycling stability (∼ 4% loss after the repetitive 2000 cycles at a charge-discharge current density of 10 mA cm(-2)).

We have successfully fabricated an asymmetric supercapacitor with high energy and power densities using graphene hydrogel (GH) with 3D interconnected pores as the negative electrode and vertically aligned MnO(2) nanoplates on nickel foam (MnO(2)-NF) as the positive electrode in a neutral aqueous Na(2)SO(4) electrolyte. Because of the desirable porous structure, high specific capacitance and rate capability of GH and MnO(2)-NF, complementary potential window of the two electrodes, and the elimination of polymer binders and conducting additives, the asymmetric supercapacitor can be cycled reversibly in a wide potential window of 0-2.0 V and exhibits an energy density of 23.2 Wh kg(-1) with a power density of 1.0 kW kg(-1). Energy density of the asymmetric supercapacitor is significantly improved in comparison with those of symmetric supercapacitors based on GH (5.5 Wh kg(-1)) and MnO(2)-NF (6.7 Wh kg(-1)). Even at a high power density of 10.0 kW kg(-1), the asymmetric supercapacitor can deliver a high energy density of 14.9 Wh kg(-1). The asymmetric supercapacitor also presents stable cycling performance with 83.4% capacitance retention after 5000 cycles.

Catalytic activity is primarily a surface phenomenon, however, little is known about Co3O4 nanocrystals in terms of the relationship between the oxygen reduction reaction (ORR) catalytic activity and surface structure, especially when dispersed on a highly conducting support to improve the electrical conductivity and so to enhance the catalytic activity. Herein, we report a controllable synthesis of Co3O4 nanorods (NR), nanocubes (NC) and nano-octahedrons (OC) with the different exposed nanocrystalline surfaces ({110}, {100}, and {111}), uniformly anchored on graphene sheets, which has allowed us to investigate the effects of the surface structure on the ORR activity. Results show that the catalytically active sites for ORR should be the surface Co2+ ions, whereas the surface Co3+ ions catalyze CO oxidation, and the catalytic ability is closely related to the density of the catalytically active sites. These results underscore the importance of morphological control in the design of highly efficient ORR catalysts.

Untethered small actuators have various applications in multiple fields. However, existing small-scale actuators are very limited in their intractability with their surroundings, respond to only a single type of stimulus and are unable to achieve programmable structural changes under different stimuli. Here, we present a multiresponsive patternable actuator that can respond to humidity, temperature and light, via programmable structural changes. This capability is uniquely achieved by a fast and facile method that was used to fabricate a smart actuator with precise patterning on a graphene oxide film by hydrogel microstamping. The programmable actuator can mimic the claw of a hawk to grab a block, crawl like an inchworm, and twine around and grab the rachis of a flower based on their geometry. Similar to the large- and small-scale robots that are used to study locomotion mechanics, these small-scale actuators can be employed to study movement and biological and living organisms.

The integration of graphene nanosheets on the macroscopic level using a self‐assembly method has been recognized as one of the most effective strategies to realize the practical applications of graphene materials. Here, a facile and scalable method is developed to synthesis two types of graphene‐based networks, manganese dioxide (MnO2)–graphene foam and carbon nanotube (CNT)–graphene foam, by solution casting and subsequent electrochemical methods. Their practical applications in flexible all‐solid‐state asymmetric supercapacitors are explored. The proposed method facilitates the structural integration of graphene foam and the electroactive material and offers several advantages including simplicity, efficiency, low‐temperature, and low‐cost. The as‐prepared MnO2–graphene and CNT–graphene electrodes exhibit high specific capacitances and rate capability. By using polymer gel electrolytes, a flexible all‐solid‐state asymmetric supercapacitor was synthesized with MnO2–graphene foam as the positive electrode and CNT‐graphene as the negative electrode. The asymmetric supercapacitors can be cycled reversibly in a high‐voltage region of 0 to 1.8 V and exhibit high energy density, remarkable rate capability, reasonable cycling performance, and excellent flexibility.