Considerable advances have been made recently in organic/polymeric electronic materials and devices. [1][2][3][4][5] These materials are useful as active layers in applications such as nonlinear optical devices, 6-8 light-emitting diodes (LED), 9,10 and thin-film field-effect transistors (FETs). [11][12][13][14][15][16][17][18][19][20] We have been studying different materials for thin-film FETs in which the active semiconductor layer consists of organic molecular or polymeric materials. 15,[19][20][21] Organic FETs have potential applications in low-cost large area flexible displays and low-end data storage devices such as smart cards. Organic materials offer numerous advantages for easy processing (e.g., spin-coating, printing, evaporation), good compatibility with a variety of substrates including flexible plastics, and great opportunities in structural modifications. 18,22 Screen printing is a simple and environment-friendly way to produce electronic circuitry and make interconnections. 23 It is a purely additive method in which ink is added where needed. Therefore, patterns can be formed in a single step. With a pitch of printed lines as fine as 250 µm, the printing process can significantly
Fabrication of unconventional energy storage devices with high stretchability and performance is challenging, but critical to practical operations of fully power-independent stretchable electronics. While supercapacitors represent a promising candidate for unconventional energy-storage devices, existing stretchable supercapacitors are limited by their low stretchability, complicated fabrication process, and high cost. Here, we report a simple and low-cost method to fabricate extremely stretchable and high-performance electrodes for supercapacitors based on new crumpled-graphene papers. Electrolyte-mediated-graphene paper bonded on a compliant substrate can be crumpled into self-organized patterns by harnessing mechanical instabilities in the graphene paper. As the substrate is stretched, the crumpled patterns unfold, maintaining high reliability of the graphene paper under multiple cycles of large deformation. Supercapacitor electrodes based on the crumpled graphene papers exhibit a unique combination of high stretchability (e.g., linear strain ~300%, areal strain ~800%), high electrochemical performance (e.g., specific capacitance ~196 F g−1), and high reliability (e.g., over 1000 stretch/relax cycles). An all-solid-state supercapacitor capable of large deformation is further fabricated to demonstrate practical applications of the crumpled-graphene-paper electrodes. Our method and design open a wide range of opportunities for manufacturing future energy-storage devices with desired deformability together with high performance.
The fabrication and characteristics of organic smart pixels are described. The smart pixel reported in this letter consists of a single organic thin-film field effect transistor (FET) monolithically integrated with an organic light-emitting diode. The FET active material is a regioregular polythiophene. The maximum optical power emitted by the smart pixel is about 300 nW/cm2 corresponding to a luminance of ∼2300 cd/m2.
The development of stretchable electronics requires the invention of compatible high-performance power sources, such as stretchable supercapacitors and batteries. In this work, two-dimensional (2D) titanium carbide (Ti 3 C 2 T x ) MXene is being explored for flexible and printed energy storage devices by fabrication of a robust, stretchable high-performance supercapacitor with reduced graphene oxide (RGO) to create a composite electrode. The Ti 3 C 2 T x /RGO composite electrode combines the superior electrochemical and mechanical properties of Ti 3 C 2 T x and the mechanical robustness of RGO resulting from strong nanosheet interactions, larger nanoflake size, and mechanical flexibility. It is found that the Ti 3 C 2 T x /RGO composite electrodes with 50 wt % RGO incorporated prove to mitigate cracks generated under large strains. The composite electrodes exhibit a large capacitance of 49 mF/cm 2 (∼490 F/cm 3 and ∼140 F/g) and good electrochemical and mechanical stability when subjected to cyclic uniaxial (300%) or biaxial (200% × 200%) strains. The as-assembled symmetric supercapacitor demonstrates a specific capacitance of 18.6 mF/cm 2 (∼90 F/cm 3 and ∼29 F/g) and a stretchability of up to 300%. The developed approach offers an alternative strategy to fabricate stretchable MXene-based energy storage devices and can be extended to other members of the large MXene family.
Biological systems can generate microstructured materials that combine organic and inorganic components and possess diverse physical and chemical properties. However, these natural processes in materials fabrication are not readily programmable. Here, we use a synthetic-biology approach to mimic such natural processes to assemble patterned materials.. We demonstrate programmable fabrication of three-dimensional (3D) materials by printing engineered self-patterning bacteria on permeable membranes that serve as a structural scaffold. Application of gold nanoparticles to the colonies creates hybrid organic-inorganic dome structures. The dynamics of the dome structures' response to pressure is determined by their geometry (colony size, dome height and pattern), which is easily modified by varying the properties of the membrane (e.g., pore size and hydrophobicity). We generate resettable pressure sensors that process signals in response to varying pressure intensity and duration.
a b s t r a c tWhereas water drops on both lotus leafs and rose petals have high contact angles, the drops can easily roll off lotus leafs but strongly adhere to rose petals. Here, we report a simple and cost-effective approach to fabricate highly stretchable large-area surfaces that give lotusleaf and rose-petal effects by harnessing origami patterns formed in graphene paper (GP) bonded on a pre-strained elastomer substrate. The surfaces of the GP origami exhibit high contact angles (>160°) yet robust adhesion to water drops. After depositing a gold film of a few nanometers on the GP, the origami of GP-Au gives high contact angle (>160°) and low roll-off angles (<5°) of water drops. We show that the high surface roughness of the GP origami leads to the high contact angle of water drops, and hydrophilic groups and defects on the GP surface significantly enhance the adhesive forces of drops on the GP origami, leading to the rose-petal effect. The coating of gold film does not affect the surface roughness of the origami but significantly reduces the adhesive force, transitioning the rose-petal to lotus-leaf effects. In addition, the wetting properties of both GP and GP-Au origamis can be tuned over a wide range by simply stretching or compressing the substrate elastomer.
Developing methods for autonomous landing of an unmanned aerial vehicle (UAV) on a mobile platform has been an active area of research over the past decade, as it offers an attractive solution for cases where rapid deployment and recovery of a fleet of UAVs, continuous flight tasks, extended operational ranges, and mobile recharging stations are desired. In this work, we present a new autonomous landing method that can be implemented on micro UAVs that require high-bandwidth feedback control loops for safe landing under various uncertainties and wind disturbances. We present our system architecture, including dynamic modeling of the UAV with a gimbaled camera, implementation of a Kalman filter for optimal localization of the mobile platform, and development of model predictive control (MPC), for guidance of UAVs. We demonstrate autonomous landing with an error of less than 37 cm from the center of a mobile platform traveling at a speed of up to 12 m/s under the condition of noisy measurements and wind disturbances.
We present a new method to fabricate semiconducting, transition metal nanoparticles (NPs) with tunable bandgap energies using engineered Escherichia coli. These bacteria overexpress the Treponema denticola cysteine desulfhydrase gene to facilitate precipitation of cadmium sulphide (CdS) NPs. Analysis with transmission electron microscopy, X-ray diffraction, and X-ray photoelectron spectroscopy reveal that the bacterially precipitated NPs are agglomerates of mostly quantum dots, with diameters that can range from 3 to 15 nm, embedded in a carbon-rich matrix. Additionally, conditions for bacterial CdS precipitation can be tuned to produce NPs with bandgap energies that range from quantum-confined to bulk CdS. Furthermore, inducing precipitation at different stages of bacterial growth allows for control over whether the precipitation occurs intra- or extracellularly. This control can be critically important in utilizing bacterial precipitation for the environmentally-friendly fabrication of functional, electronic and catalytic materials. Notably, the measured photoelectrochemical current generated by these NPs is comparable to values reported in the literature and higher than that of synthesized chemical bath deposited CdS NPs. This suggests that bacterially precipitated CdS NPs have potential for applications ranging from photovoltaics to photocatalysis in hydrogen evolution.
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