High-Electrification Performance and Mechanism of a Water-Solid Mode Triboelectric Nanogenerator.

With the advantages of superior wear resistance, mechanical durability, and stability, the liquid-solid mode triboelectric nanogenerator (TENG) has been attracting much attention in the field of energy harvesting and self-powered sensors. However, most reports are primarily observational, and there still lacks a universal model of this kind of TENG. Here, an equivalent circuit model and corresponding governing equations of a water-solid mode TENG are developed, which could easily be extended to other types of liquid-solid mode TENGs. Based on the first-order lumped circuit theory, the full equivalent circuit model of water-solid mode TENG is modeled as a series connection of two capacitors and a water resistor. Accordingly, its output characteristics and critical influences are examined, to investigate the relevant physical mechanism behind them. Afterward, a three-dimensional water-solid TENG array constructed from many single-wire TENGs is fabricated, which can not only harvest tiny amounts of energy from any movement of water, but also can verify our theoretical predictions. The fundamentals of the water-solid mode TENG presented in this work could contribute to solving the problem of electrical phenomena on a liquid-solid interface, and may establish a sound basis for a thorough understanding of the liquid-solid mode TENG.

Tuning the band gap in silicene by oxidation.

Silicene monolayers grown on Ag(111) surfaces demonstrate a band gap that is tunable by oxygen adatoms from semimetallic to semiconducting type. With the use of low-temperature scanning tunneling microscopy, we find that the adsorption configurations and amounts of oxygen adatoms on the silicene surface are critical for band gap engineering, which is dominated by different buckled structures in √13 × âˆš13, 4 × 4, and 2√3 × 2√3 silicene layers. The Si-O-Si bonds are the most energy-favored species formed on √13 × âˆš13, 4 × 4, and 2√3 × 2√3 structures under oxidation, which is verified by in situ Raman spectroscopy as well as first-principles calculations. The silicene monolayers retain their structures when fully covered by oxygen adatoms. Our work demonstrates the feasibility of tuning the band gap of silicene with oxygen adatoms, which, in turn, expands the base of available two-dimensional electronic materials for devices with properties that is hardly achieved with graphene oxide.