Ion-Incorporative, Degradable Nanocellulose Crystal Substrate for Sustainable Carbon-Based Electronics.

Electronic wastes from transient electronics accumulate biologically harmful materials with global concern. Recycling these wastes could prevent the deposition of hazardous chemicals and toxic materials to the environment while saving scarce natural compounds and valuable resources. Here, we report a sustainable electronic device, taking advantage of carbon resources and a biodegradable cellulose composite. The device consists of an ambient-stable carbon nanotube as a semiconductor, graphene as electrodes, and a free-standing cellulose filter paper/nanocellulose composite as a dielectric layer. The dual-functional cellulose composite acting simultaneously as a robust substrate and a dielectric is demonstrated, which is compatible with solution device fabrication processes. An optimized channel dimension of 5 mm × 3 mm with the addition of ions that facilitates a charge transport realized a device with an on-current per width of 9.6 µA mm-1, an on/off ratio >102, a field-effect mobility of 2.03 cm2 V-1 s-1, and long-term stability over 30 days under ambient conditions. Successful separation of the carbonaceous components via an eco-friendly solution sorting protocol allowed the recycled device to display excellent electronic performance, with a recapture efficiency of 90%. This effort demonstrates a processable, low-cost, and sustainable electronic system that can be applied in the current realm of the semiconducting and sensing industry.

Highly Aligned Array of Heterostructured Polyflourene-Isolated Boron Nitride and Carbon Nanotubes.

Boron nitride nanotubes (BNNTs) have attracted increasing attention for their exceptional thermal, electronic, and optical properties. However, the progress in BNNTs applications has largely been limited by the low purity of as-synthesized BNNTs and inefficient solution-processing protocols due mainly to the instability of BNNTs in most of the solvents. Therefore, fabrication of highly pure, stable, and fully individualized BNNTs in a rational manner is required. Here, we report a significant improvement in the preparation of well-dispersed BNNTs, utilizing conjugated polymers that interact with BNNTs, allowing selective sorting and individualization of the nanotubes. Evidence of strong interactions between the polymers and BNNTs was observed by optical absorption and photoluminescence spectroscopies, while effective individualization was observed by electron microscopy. The sorted BNNTs were successfully used in a solution-processing protocol called dose-controlled, floating evaporative self-assembly (DFES) previously established for single-walled carbon nanotubes (SWCNT) array fabrication. A device fabricated via DFES from the sorted BNNTs mixed with polymer-wrapped, semiconducting single-walled carbon nanotubes (s-SWCNTs) exhibited an on-state conductance of 253 ± 6 µS µm-1 and an on/off ratio of 106.6±0.4 for a gate voltage of -0.1 V. This breakthrough in BNNT dispersion and isolation is a significant advancement toward the exploitation of BNNTs in future applications.

Role of small leucine zipper protein in hepatic gluconeogenesis and metabolic disorder.

Hepatic gluconeogenesis is the central pathway for glucose generation in the body. The imbalance between glucose synthesis and uptake leads to metabolic diseases such as obesity, diabetes, and cardiovascular diseases. Small leucine zipper protein (sLZIP) is an isoform of LZIP and it mainly functions as a transcription factor. Although sLZIP is known to regulate the transcription of genes involved in various cellular processes, the role of sLZIP in hepatic glucose metabolism is not known. In this study, we investigated the regulatory role of sLZIP in hepatic gluconeogenesis and its involvement in metabolic disorder. We found that sLZIP expression was elevated during glucose starvation, leading to the promotion of phosphoenolpyruvate carboxylase and glucose-6-phosphatase expression in hepatocytes. However, sLZIP knockdown suppressed the expression of the gluconeogenic enzymes under low glucose conditions. sLZIP also enhanced glucose production in the human liver cells and mouse primary hepatic cells. Fasting-induced cyclic adenosine monophosphate impeded sLZIP degradation. Results of glucose and pyruvate tolerance tests showed that sLZIP transgenic mice exhibited abnormal blood glucose metabolism. These findings suggest that sLZIP is a novel regulator of gluconeogenic enzyme expression and plays a role in blood glucose homeostasis during starvation.

Making Nonconjugated Small-Molecule Organic Radicals Conduct.

Charge neutral, nonconjugated organic radicals have emerged as extremely useful active materials for solid-state electronic applications. This previous achievement confirmed the potential of radical-based macromolecules in organic electronic devices; however, charge transport in radical molecules has not been studied in great detail from a fundamental perspective. Here we demonstrate the charge transport in a nonconjugated organic small radical, 4-hydroxy-2,2,6,6-tetramethylpiperidin-1-oxyl (h-TEMPO). The chemical component of this radical molecule allows us to form a single crystal via physical vapor deposition (PVD). While the charge transport of this macroscopic open-shell single crystal is rather low, thermal annealing of the well-defined single crystal enables the molecule to have a rapid charge transfer reaction due to the electronic communication of open-shell sites with each other, which results in electrical conductivities greater than 0.05 S m-1. This effort demonstrates a drastically different model than the commonly accepted conjugated polymers or molecules for the creation of next-generation conductors.