Freestanding nanowires have ultrahigh elastic strain limits (4 to 7%) and yield strengths, but exploiting their intrinsic mechanical properties in bulk composites has proven to be difficult. We exploited the intrinsic mechanical properties of nanowires in a phase-transforming matrix based on the concept of elastic and transformation strain matching. By engineering the microstructure and residual stress to couple the true elasticity of Nb nanowires with the pseudoelasticity of a NiTi shape-memory alloy, we developed an in situ composite that possesses a large quasi-linear elastic strain of over 6%, a low Young's modulus of ~28 gigapascals, and a high yield strength of ~1.65 gigapascals. Our elastic strain-matching approach allows the exceptional mechanical properties of nanowires to be exploited in bulk materials.

Both the ligand effect and surface strain can affect the electrocatalytic reactivity. In that matter exists a need to be fundamentally understood; however, there is no effective strategy to isolate the strain effect in electrocatalytic systems. In this research we show how the elastic strain in a platinum nanofilm varies the catalytic activity for the oxygen reduction reaction, a key barrier to the wide applications of fuel cells. NiTi shape memory alloy was selected as the substrate to strain engineer the deposited Pt nanofilm in both compressively and tensilely strained states by taking advantage of the two-way shape memory effect for the first time. We demonstrate that compressive strain weakens the Pt surface adsorption and hence improves the ORR activity, which reflects in a 52% enhancement of the kinetic rate constant and a 27 mV positive shift of the half-wave potential for the compressively strained 5 nm Pt compared to the pristine Pt. Tensile strain has the opposite effect, which is in general agreement with the proposed d-band theory.

Soft actuators with perception capability are essential for robots to intelligently interact with humans and the environment. However, existing perceptive soft actuators require complex integration and coupling between the discrete functional units to achieve autonomy. Here, we report entirely soft actuators with embodied sensing, actuation, and control at the single-unit level. This is achieved by synergistically harnessing the mechanosensing and electrothermal properties of liquid metal (LM) to actuate the thermally responsive liquid crystal elastomer (LCE). We create multifunctional LM circuits on the LCE surface using a simple and facile methodology based on magnetic printing. The fluidic LM circuit can not only be utilized as a conformable resistive heater but also as a sensory skin to perceive its own deformation. Moreover, the rational design of the LM circuits makes it possible to achieve biomimetic autonomous actuation in response to mechanical stimuli such as pressure or strain. In addition, the intrinsic stretchability of LM allows us to create 3D spring-like actuators via a simple prestretch step, and complex helical motions can be obtained upon mechanical stimulation. This work provides a unique and simple design for autonomous soft robotics with embodied intelligence.

No abstract

a b s t r a c t N-doped TiO 2 nanowire/N-doped graphene (NeTiO 2 /NG) heterojunctions are fabricated by a simple hydrothermal method in a solution containing urea. In this hybrid structure, a three-dimensional hybrid photocatalyst was fabricated by using one-dimensional N-doped TiO 2 nanowires penetrating through twodimensional graphene nanosheets. Compared with TiO 2 nanowire/graphene and N-doped TiO 2 nanowire/ graphene composites, the NeTiO 2 /NG heterostructures demonstrate a better photocatalytic performance for the degradation of methylene blue under visible light irradiations, as well as displaying a better recyclability. It is found that the nitrogen atoms originated from the decomposition of urea were not only entered into the lattice of TiO 2 nanowires but also doped into the skeleton of graphene nanosheets. Results show that N doping expands the visible light absorption region of TiO 2 , and N-doped graphene additionally improves the separation and transportation of photogenerated electronehole pairs plus generating a higher photocurrent, which plays a critical role for enhancing the photocatalytic activity.