Triboelectrification is a well-known phenomenon that commonly occurs in nature and in our lives at any time and any place. Although each and every material exhibits triboelectrification, its quantification has not been standardized. A triboelectric series has been qualitatively ranked with regards to triboelectric polarization. Here, we introduce a universal standard method to quantify the triboelectric series for a wide range of polymers, establishing quantitative triboelectrification as a fundamental materials property. By measuring the tested materials with a liquid metal in an environment under well-defined conditions, the proposed method standardizes the experimental set up for uniformly quantifying the surface triboelectrification of general materials. The normalized triboelectric charge density is derived to reveal the intrinsic character of polymers for gaining or losing electrons. This quantitative triboelectric series may serve as a textbook standard for implementing the application of triboelectrification for energy harvesting and self-powered sensing.

A long debate on the charge identity and the associated mechanisms occurring in contact-electrification (CE) (or triboelectrification) has persisted for many decades, while a conclusive model has not yet been reached for explaining this phenomenon known for more than 2600 years! Here, a new method is reported to quantitatively investigate real-time charge transfer in CE via triboelectric nanogenerator as a function of temperature, which reveals that electron transfer is the dominant process for CE between two inorganic solids. A study on the surface charge density evolution with time at various high temperatures is consistent with the electron thermionic emission theory for triboelectric pairs composed of Ti-SiO and Ti-Al O . Moreover, it is found that a potential barrier exists at the surface that prevents the charges generated by CE from flowing back to the solid where they are escaping from the surface after the contacting. This pinpoints the main reason why the charges generated in CE are readily retained by the material as electrostatic charges for hours at room temperature. Furthermore, an electron-cloud-potential-well model is proposed based on the electron-emission-dominatedcharge-transfer mechanism, which can be generally applied to explain all types of CE in conventional materials.

The storage/utilization of solar energy is a promising strategy to alleviate current disparities in energy shortage Direct conversion of solar light into chemical energy by means of photocatalysis or photoelectrocatalysis is currently a point of focus for sustainable energy development and environmental remediation. However, its current efficiency is still far from satisfying, suffering especially from severe charge recombination. To solve this problem, the piezo-phototronic effect has emerged as one of the most effective strategies for photo(electro)catalysis. Through the integration of piezoelectricity, photoexcitation, and semiconductor properties, the built-in electric field by mechanical stimulation induced polarization can serve as a flexible autovalve to modulate the charge-transfer pathway and facilitate carrier separation both in the bulk phase and at the surfaces of semiconductors. This review focuses on illustrating the trends and impacts of research based on piezo-enhanced photocatalytic reactions. The fundamental mechanisms of piezo-phototronics modulated band bending and charge migration are highlighted. Through comparing and classifying different categories of piezo-photocatalysts (like the typical ZnO, MoS 2 , and BaTiO 3 ), the recent advances in polarization-promoted photo(electro)catalytic processes involving water splitting and pollutant degradation are overviewed. Meanwhile the optimization methods to promote their catalytic activities are described. Finally, the outlook for future development of polarization-enhanced strategies is presented.

Contact-electrification is a universal effect for all existing materials, but it still lacks a quantitative materials database to systematically understand its scientific mechanisms. Using an established measurement method, this study quantifies the triboelectric charge densities of nearly 30 inorganic nonmetallic materials. From the matrix of their triboelectric charge densities and band structures, it is found that the triboelectric output is strongly related to the work functions of the materials. Our study verifies that contact-electrification is an electronic quantum transition effect under ambient conditions. The basic driving force for contact-electrification is that electrons seek to fill the lowest available states once two materials are forced to reach atomically close distance so that electron transitions are possible through strongly overlapping electron wave functions. We hope that the quantified series could serve as a textbook standard and a fundamental database for scientific research, practical manufacturing, and engineering.

Triboelectric nanogenerators (TENGs) are attracting more and more attention since they can convert various mechanical energies into electric energy. However, in traditional TENGs for harvesting rotation energy, most of the contacts between two triboelectric materials are rigid-to-rigid contact with very large friction force, which limits their practical application. Here, we report an ultra-low-friction triboelectric-electromagnetic hybrid nanogenerator (NG). A freestanding mode TENG and a rotating electromagnetic generator (EMG) are integrated together to realize the complementary individual merits. The very soft and elastic contact between the two triboelectric materials in the TENG results into very small friction force. The influences of the type and the dimensions of the dielectric material on the performance of the TENG are studied systematically from theory to experiments. The results indicate that the open-circuit voltage and the transfer charge of the TENG increase with the rotation speed, which is very different from a traditional rotary TENG and is due to the increase of the contact area. The optimized TENG has a maximal load voltage of 65 V and maximal load power per unit mass of 438.9 mW/kg under a speed rotation of 1000 rpm, while the EMG has a maximal load voltage of 7 V and maximal load power density of 181 mW/kg. This demonstration shows that the hybrid NG can power a humidity/temperature sensor by converting wind energy into electric energy when the wind speed is 5.7 m/s. Meanwhile, it can be used as a self-powered wind speed sensor to detect wind speed as low as 3.5 m/s.