Stable water-floating transistor with recyclability.

Electronic wastes from used devices containing environmentally hazardous materials are an immediate concern for the sustainable development of electronic and sensor industries. To address this, a highly controllable and dedicated electronic module should be devised, that allows systematic recollection of as many components from the original device for their reuse. Here, we report the total recycling of an electronic device, exploiting a water-floating system that is based on a water-compatible semiconductor as an active material.

Mapping Out the Nonconjugated Organic Radical Conductors via Chemical or Physical Pathways.

Stable, nitroxide-based organic radicals have gained tremendous attention in a wide range of research fields, ranging from solid-state electronics to energy storage devices. While the success of these organics has been their designer flexibility and the processability that can fully potentiate the open-shell chemistry, a significant knowledge gap exists on the solid-state electronics of small-molecular radicals. Herein, we examine the structure-property relationship that governs the solid-state electronics of a model nitroxide and its derivatives by seeking the connection to their well-established, electrolyte-based chemistry.

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.

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).