Chemically Engineered Titanium Oxide Interconnecting Layer for Multijunction Polymer Solar Cells.

We report chemically tunable n-type titanium oxides using ethanolamine as a nitrogen dopant source. As the amount of ethanolamine added to the titanium oxide precursor during synthesis increases, the Fermi level of the resulting titanium oxides (ethanolamine-incorporated titanium oxides) significantly changes from -4.9 eV to -4.3 eV, and their free charge carrier densities are enhanced by two orders of magnitudes, reaching up to 5 × 1018 cm-3. Unexpectedly, a basic ethanolamine reinforces not only the n-type properties of titanium oxides, but also their basicity, which facilitates acid-base ionic junctions in contact with acidic materials. The enhanced charge carrier density and basicity of the chemically tuned titanium oxides enable multi-junction solar cells to have interconnecting junctions consisting of basic n-type titanium oxides and acidic p-type PEDOT:PSS to gain high open-circuit voltages of 1.44 V and 2.25 V from tandem and triple architectures, respectively.

Highly Water-Dispersible Graphene Nanosheets From Electrochemical Exfoliation of Graphite.

The electrochemical exfoliation of graphite has been considered to be an effective approach for the mass production of high-quality graphene due to its easy, simple, and eco-friendly synthetic features. However, water dispersion of graphene produced in the electrochemical exfoliation method has also been a challenging issue because of the hydrophobic properties of the resulting graphene. In this study, we report the electrochemical exfoliation method of producing water-dispersible graphene that importantly contains the relatively low oxygen content of <10% without any assistant dispersing agents. Through the mild in situ sulfate functionalization of graphite under alkaline electrochemical conditions using a pH buffer, the highly water-dispersible graphene could be produced without any additional separation processes of sedimentation and/or centrifugation. We found the resulting graphene sheets to have high crystalline basal planes, lateral sizes of several µm, and a thickness of <5 nm. Furthermore, the high aqueous dispersion stability of as-prepared graphene could be demonstrated using a multi-light scattering technique, showing very little change in the optical transmittance and the terbiscan stability index over time.

All-printed nanomembrane wireless bioelectronics using a biocompatible solderable graphene for multimodal human-machine interfaces.

Recent advances in nanomaterials and nano-microfabrication have enabled the development of flexible wearable electronics. However, existing manufacturing methods still rely on a multi-step, error-prone complex process that requires a costly cleanroom facility. Here, we report a new class of additive nanomanufacturing of functional materials that enables a wireless, multilayered, seamlessly interconnected, and flexible hybrid electronic system. All-printed electronics, incorporating machine learning, offers multi-class and versatile human-machine interfaces. One of the key technological advancements is the use of a functionalized conductive graphene with enhanced biocompatibility, anti-oxidation, and solderability, which allows a wireless flexible circuit. The high-aspect ratio graphene offers gel-free, high-fidelity recording of muscle activities. The performance of the printed electronics is demonstrated by using real-time control of external systems via electromyograms. Anatomical study with deep learning-embedded electrophysiology mapping allows for an optimal selection of three channels to capture all finger motions with an accuracy of about 99% for seven classes.

CO2-activated, hierarchical trimodal porous graphene frameworks for ultrahigh and ultrafast capacitive behavior.

Herein, we demonstrate CO2-activated macroscopic graphene architectures with trimodal pore systems that consist of 3D inter-networked macroporosity arising from self-assembly, mesoporosity arising from the intervoids of nanosheets, and microporosity via CO2 activation. The existence of micropores residing in hierarchical structures of trimodal porous graphene frameworks (tGFs) contributes to greatly improve the surface area and pore volume, which are ∼3.8 times greater than typical values of existing 3D macroporous graphene monoliths. As confirmed by the specific capacity, the kinetic parameters, and the regeneration capability for chemical adsorption as well as the specific capacitance, the rate capability, and the cycle stability for electrochemical energy storage, the tGFs have an ideal texture for high performance capacitive materials. Furthermore, the tGFs obtain the structurally and energetically homogeneous surface active sites, which dominantly operate through the π-π interactions for adsorption. Consequently, the ultrahigh capacitance and ultrafast capacitive performance of the tGFs for both chemical and electrochemical adsorptions are attributed to hierarchical trimodal porosity and surface chemistry. These results offer a chemical approach combining self-assembly with conventional activation for the construction of 3D hierarchical structures with multimodal porosity.

Study on the origin of amorphous carbon peaks on graphene films synthesized on nickel catalysts.

We present our investigation results on the origin of the morphological defects on graphene films synthesized by chemical vapor deposition method on nickel catalytic substrates. These defects are small-base-area (SBA) peaks with tens of nanometer heights, and they diminish the applicability of graphene films. From atomic force microscopy observations on the graphene films prepared in various ways, we found that significant portion of the SBA peaks is formed in the crevices on the nickel substrates. Our results may be useful for developing an efficient synthesis method to produce high-quality graphene films without the SBA peaks.

Confining grains of textured Cu2O films to single-crystal nanowires and resultant change in resistive switching characteristics.

By confining columnar grains of textured oxide film using anodized aluminum oxide template, we could obtain a grain-boundary-free (GB-free) cuprous oxide (Cu(2)O) nanowire arrays with a narrow diameter distribution and a high density under the same electrochemical deposition condition. A two-terminal device fabricated using an individual GB-free nanowire and Au/Cr electrodes exhibits bipolar resistive switching contrary to the unipolar one of a textured film, and Schottky-like conduction. On the other hand, a nanowire device with Pt electrodes reveals non-switching behavior and Ohmic conduction. Thus, we can propose that the bipolar switching of a nanowire device with Au/Cr electrodes may result from the modulation of Schottky barrier at the interface by migration of oxygen vacancies while the unipolar one of a textured film may be defined as the bulky filamentary switching along the GBs in the GB-embedded texture films.