Systematic Doping Control of CVD Graphene Transistors with Functionalized Aromatic Self‐Assembled Monolayers

Recent reports have shown that self‐assembled monolayers (SAMs) can induce doping effects in graphene transistors. However, a lack of understanding persists surrounding the quantitative relationship between SAM molecular design and its effects on graphene. In order to facilitate the fabrication of next‐generation graphene‐based devices it is important to reliably and predictably control the properties of graphene without negatively impacting its intrinsic high performance. In this study, SAMs with varying dipole magnitudes/directions are utilized and these values are directly correlated to changes in performance seen in graphene transistors. It is found that, by knowing the z‐component of the SAM dipole, one can reliably predict the shift in graphene charge neutrality point after taking into account the influence of the metal electrodes (which also play a role in doping graphene). This relationship is verified through density functional theory and comprehensive device studies utilizing atomic force microscopy, X‐ray photoelectron spectroscopy, Raman spectroscopy, and electrical characterization of graphene transistors. It is shown that properties of graphene transistors can be predictably controlled with SAMs when considering the total doping environment. Additionally, it is found that methylthio‐terminated SAMs strongly interact with graphene allowing for a cleaner graphene transfer and enhanced charge mobility.     

Multimodal Magneto‐Plasmonic Nanoclusters for Biomedical Applications

Multimodal nanostructures can help solve many problems in the biomedical field including sensitive molecular imaging, highly specific therapy, and early cancer detection. However, the synthesis of densely packed, multicomponent nanostructures with multimodal functionality represents a significant challenge. Here, a new type of hybrid magneto‐plasmonic nanoparticles is developed using an oil‐in‐water microemulsion method. The nanostructures are synthetized by self‐assembly of primary 6 nm iron oxide core‐gold shell particles resulting into densely packed spherical nanoclusters. The dense packing of primary particles does not change their superparamagnetic behavior; however, the close proximity of the constituent particles in the nanocluster leads to strong near‐infrared (NIR) plasmon resonances. The synthesis is optimized to eliminate nanocluster cytotoxicity. Immunotargeted nanoclusters are also developed using directional conjugation chemistry through the Fc antibody moiety, leaving the Fab antigen recognizing region available for targeting. Cancer cells labeled with immunotargeted nanoclusters produce a strong photoacoustic signal in the NIR that is optimum for tissue imaging. Furthermore, the labeled cells can be efficiently captured using an external magnetic field. The biocompatible magneto‐plasmonic nanoparticles can make a significant impact in development of point‐of‐care assays for detection of circulating tumor cells, as well as in cell therapy with magnetic cell guidance and imaging monitoring.     

Membrane‐Based Self‐Powered Triboelectric Sensors for Pressure Change Detection and Its Uses in Security Surveillance and Healthcare Monitoring

A new membrane‐based triboelectric sensor (M‐TES) is presented as a self‐powered pressure change sensor. It generates a voltage induced by surface triboelectric charges in response to an air pressure change. Extremely high detection resolutions of 0.34 Pa and 0.16 Pa are achieved when the air pressure increases and decreases in a small region away from the ambient standard atmosphere pressure, respectively, indicating an excellent sensitivity. By integrating the M‐TES with a signal processing unit, we demonstrate practical applications of the device in sensing footsteps, respirations, and heartbeat, which suggests widespread use of the M‐TES in fields of security surveillance, chemical engineering, geography research, environment monitoring, and personal healthcare.     

Controlled Incorporation of Ni(OH)2 Nanoplates Into Flowerlike MoS2 Nanosheets for Flexible All‐Solid‐State Supercapacitors

In this work, self‐supporting three‐dimensional hierarchical nanostructured MoS₂@Ni(OH)₂ nanocomposites are synthesized via a facile single‐mode microwave hydrothermal technique. The fabricated MoS₂@Ni(OH)₂ nanocomposites for supercapacitors in aqueous electrolyte exhibit higher specific capacitance and better cyclic stability than those of MoS₂ and Ni(OH)₂ due to the pronounced synergistic effect between MoS₂ and Ni(OH)₂. Further, the flexible all‐solid‐state supercapcitor is readily constructed by composing the PVA/KOH gel electrolyte in between two MoS₂@Ni(OH)₂ electrodes on the flexible PET substrates. The resulting supercapacitors can operate at high rate up to 1000 V/s, have excellent long‐life cycling stability, retaining 94.2% of the initial capacitance after 9000 cycles, and mechanical flexibility during extreme bending, respectively. Thereby, the MoS₂@Ni(OH)₂ nanocomposites are a promising electrode materials for flexible long‐life cycling all‐solid‐sate supercapacitors.     

Self‐Healing Reduced Graphene Oxide Films by Supersonic Kinetic Spraying

The industrial scale application of graphene and other functional materials in the field of electronics has been limited by inherent defects, and the lack of simple deposition methods. A simple spray deposition method is developed that uses a supersonic air jet for a commercially available reduced graphene oxide (r‐GO) suspension. The r‐GO flakes are used as received, which are pre‐annealed and pre‐hydrazine‐treated, and do not undergo any post‐treatment. A part of the considerable kinetic energy of the r‐GO flakes entrained by the supersonic jet is used in stretching the flakes upon impact with the substrate. The resulting “frozen elastic strains” heal the defects (topological defects, namely Stone‐Wales defect and C₂ vacancies) in the r‐GO flakes, which is reflected in the reduced ratio of the intensities of the D and G bands in the deposited film. The defects can also be regenerated by annealing.     

Gyroid‐Structured 3D ZnO Networks Made by Atomic Layer Deposition

3D continuous ZnO morphologies with characteristic feature sizes on the 10 nm length scale are attractive for electronic device manufacture. However, their synthesis remains a challenge because of the low crystallization temperature of ZnO. Here, we report a method for the robust and reliable synthesis of fully crystalline 3D mesoporous ZnO networks by means of atomic layer deposition (ALD) of ZnO into a self‐assembled block copolymer template. By carefully optimizing the processing conditions we are able to synthesize several‐micrometer‐thick layers of mesoporous ZnO networks with a strut width of 30 nm. Two 3D mesoporous morphologies are manufactured: a periodic gyroid structure and a random worm‐like morphology. Exploiting the ALD property to conformally coat complex surfaces of high aspect ratio, the channel network of a 3D continuous channel network of a self‐assembled block copolymer is replicated into ZnO. X‐ray photoemission spectroscopy and x‐ray diffraction measurements reveal that the chemical composition of the mesoporous structures is uniform and consists of wurtzite‐ZnO throughout the film. Scanning electron microscopy reveals an average pore dimension of 30 nm. The potential of this material for a hybrid photovoltaic application is demonstrated by the manufacture of a poly(3‐hexylthiophene)/ZnO solar cell.     

Triboelectric Nanogenerator as an Active UV Photodetector

Self‐powered nanosensors and nanosystems have attracted significant attention in the past decades and have gradually become the most desirable and promising prototype for environmental protection/detection because no battery is needed to power the device. Therefore, in this paper a design is proposed for a self‐powered photodetector based on triboelectric nanogenerator (TENG) configuration. 3D dendritic TiO₂ nanostructures are synthesized as the built‐in UV photodetector as well as the contact material of the TENG. The cost‐effective, robust, and easily fabricated TENG‐based photodetector presents superior photoresponse characteristics, which include an excellent responsivity over 280 A W^?1, rapid rise time (18 ms) and decay time (31 ms), and a wide detection range of light intensity from 20 μW cm^?2 to 7 mW cm^?2. In the last part of the paper, a stand‐alone and self‐powered environmental sensing device is developed by applying poly(methyl methacrylate) (PMMA) substrates and springs to assemble the TENG‐based photodetector. These results indicate that the new prototype sensing device based on the TENG configuration shows great potential as a self‐powered photodetector.     

Direct‐Current Triboelectric Generator

The first direct‐current triboelectric generator (DC‐TEG) based on sliding electrification for harvesting mechanical energy from rotational motion is reported. The DC‐TEG consists of two rotating wheels and one belt for connecting them, which are made of distinctly different triboelectric materials with a specific requirement. During the rotation, the contact‐induced electrification and the relative sliding between the two wheels and the belt can induce a continuous increase of the accumulated positive and negative triboelectric charges at the two rotating wheels, respectively, resulting in a Corona discharge and producing the observed current through an external load. The DC‐TEG can deliver an open‐circuit voltage of larger than 3200 V and a maximum power of 100 μW under an external load of 60 MΩ at a rotational speed of 1000 r min^–1. By designing a point metal discharge electrode near the accumulated positive charges on the metal wheel, the instantaneous short‐circuit current can be up to 0.37 mA. The DC‐TEG can be utilized as a direct power source to light up 1020 serially connected commercial light‐emitting diodes (LEDs) and the produced energy can also be stored in a capacitor for other uses. This work presents a DC‐TEG technology to harvest mechanical energy from rotational motion for self‐powered electronics.     

Self‐Powered Trajectory,Velocity, and Acceleration Tracking of a Moving Object/Body using a Triboelectric Sensor

Motion tracking is of great importance in a wide range of fields such as automation, robotics, security, sports and entertainment. Here, a self‐powered, single‐electrode‐based triboelectric sensor (TES) is reported to accurately detect the movement of a moving object/body in two dimensions. Based on the coupling of triboelectric effect and electrostatic induction, the movement of an object on the top surface of a polytetrafluoroethylene (PTFE) layer induces changes in the electrical potential of the patterned aluminum electrodes underneath. From the measurements of the output performance (open‐circuit voltage and short‐circuit current), the motion information about the object, such as trajectory, velocity, and acceleration is derived in conformity with the preset values. Moreover, the TES can detect motions of more than one objects moving at the same time. In addition, applications of the TES are demonstrated by using LED illuminations as real‐time indicators to visualize the movement of a sliding object and the walking steps of a person.