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The high‐efficiency conversion of water drop mechanical energy into electrical energy has always been an urgent issue in the development and utilization of raindrop energy. In this work, a novel drum‐like triboelectric nanogenerator (D‐TENG) with robust self‐cleaning superhydrophobic features is developed to harvest water drop energy. An elastic superhydrophobic cellulose paper is created by spray‐coating nanofumed silica dispersed in a thermoplastic elastomer solution, followed by treatment with triethoxy‐1H,1H,2H,2H‐tridecafluoro‐n‐octylsilane. When raindrops hit the D‐TENG surface, the superhydrophobic cellulose paper will vibrate and periodic contact and separation with polytetrafluoroethylene will occur to generate electricity. The results demonstrate that when a 6 mm water drop falls from a height of 2.5 m and hits the D‐TENG, the generated voltage output can reach a peak of 21.6 V and charge transfer of 10 nC. The output power of the D‐TENG can reach 16 µW per droplet, which is more than 13.3 times that generated from the previous TENGs based on the electrostatic induction of water droplets. These results indicate that the superhydrophobic cellulose paper‐based D‐TENG is potentially a strong candidate for harvesting energy from raindrops, thereby making it a promising sustainable energy source for next‐generation electronics. [ABSTRACT FROM AUTHOR]

The rapid development of wearable electronics has placed higher demands on the design strategies of triboelectric materials. Aerogels have the potential to become advanced triboelectric materials, however, traditional design strategies often require complex processes and additional chemical cross‐linking agents to improve the stability of the gel structure, which limits its practical application. In this work, a scalable and sustainable self‐assembly drive strategy is proposed for the design of bio‐based triboelectric aerogels with multi‐scale winding structures. Interestingly, the autoacceleration effect, which is regarded as "unfavorable" during the autocatalytic polymerization of supramolecules, is rationally exploited to provide the supramolecules within the matrix with an abundance of multiple hydrogen bonds at the same time as their rapid gelation occurs. Thanks to this, the aerogel film exhibits ultra‐high tensile strength (104 MPa) and remains undeformed after resisting an impact of 8000 times its own weight. Highly robust triboelectric aerogel films are used to build wearable self‐powered sensors with ultra‐fast response in complex environments (48 ms), while enabling real‐time interaction between the wearer and the information network. The design idea of " turning a detriment into an asset " in this work provides a new idea for the material construction of highly robust wearable sensors. [ABSTRACT FROM AUTHOR]

Non‐contact intelligent sensing technology is a key player in the data acquisition and environmental monitoring framework of the Internet of Everything, laying the groundwork for the realization of highly integrated intelligent network systems. However, environmental factors continue to be a major challenge in the process of real‐time monitoring and feedback of objects, constraining the stability and accuracy of the sensing signals. In this study, a hierarchical spatial assembly strategy is implemented to effectively integrate an intermediate energy storage layer with superhydrophobic surfaces (CA = 162 ± 2.5°), resulting in the development of a moisture‐resistant triboelectric structural materials with stable monitoring and tracking capabilities. The moisture‐resistant self‐powered sensor constructed from this triboelectric structural material operates effectively in extreme humidity conditions (99% RH) with a full‐scale output retention rate of 95.2%, and is capable of accurately sensing human activity from the distance of 3 m. Importantly, the sensor can also effectively detect vehicle states during operation and perform real‐time monitoring of the vehicle's surrounding environment. This study not only overcomes the long‐standing challenges of accuracy and stability in high humidity for sensors but also advances the development of sustainable, interconnected intelligent systems for the Internet of Everything in extreme environmental conditions. [ABSTRACT FROM AUTHOR]

The advent of self‐powered wearable electronics will revolutionize the fields of smart healthcare and sports monitoring. This technological advancement necessitates more stringent design requirements for triboelectric materials. The triboelectric aerogels must enhance their mechanical properties to address the issue of structural collapse in real‐world applications. This study fabricates stiff nanocellulosic triboelectric aerogels with multiscale structures induced by the Hofmeister effect. The aggregation and crystallization of polymer molecular chains are enhanced by the Hofmeister effect, while ice crystal growth imparts a porous structure to the aerogel at the micron scale. Therefore, the triboelectric aerogel exhibits exceptional stiffness, boasting a Young's modulus of up to 142.9 MPa and a specific modulus of up to 340.6 kN m kg–1, while remaining undeformed even after supporting 6600 times its weight. Even after withstanding an impact of 343 kPa, highly robust wearable self‐powered sensors fabricated with triboelectric aerogels remain operational. Additionally, the self‐powered sensor is capable of accurately detecting human movements, particularly in abnormal fall postures detection. This study provides considerable research and practical value for promoting material design and broadening application scenarios for self‐powered wearable electronics. [ABSTRACT FROM AUTHOR]

[Display omitted] Triboelectric nanogenerators (TENGs), as a new energy conversion device in self-powered sensing devices, have been used at extreme environmental conditions, which poses great challenges to the structural stability and chemical tolerance of triboelectric materials. However, the low tolerance characteristics of traditional triboelectric materials limit their expansion in emerging applications. Cellulose, with its unique multidimensional structure and, controlled surface chemistry regulation advantages, shows great potential in resisting extreme environmental conditions and is emerging as a new candidate. This review aims to design and fabricate cellulosic triboelectric materials with exceptional tolerance, providing a perspective on the emerging applications of TENGs at extreme environmental conditions. First, the performance advantages and design principles of action of cellulosic triboelectric materials at extreme environmental conditions are described. Second, the importance of physical and chemical regulation strategies is discussed through the multi-scale perspective from macroscopic fiber bundles to microscopic cellulose molecules. It also presents the latest applications of cellulosic triboelectric materials at extreme environmental conditions such as wide temperature, high humidity, high corrosion, and radiation. Finally, the idea of how cellulosic triboelectric materials can further expand the development of TENGs application areas is presented. [ABSTRACT FROM AUTHOR]

Gas‐sensitive materials are capable of dynamic identification and content monitoring of specific gases in the environment, and their applications in the field of gas sensing are promising. However, weak adsorption properties are the main challenge limiting the application of gas‐sensitive materials. A highly adsorbent gas‐sensitive cellulose nanofibril (CNF)‐based triboelectric material with a layered structure is prepared here and it is applied to self‐powered gas sensing. The layered structure of the triethoxy‐1H,1H,2H,2H‐tridecafluoro‐n‐octylsilane cellulose nanofiber (PFOTES‐CNF)‐based gas‐sensitive material further enhances the adsorption of the material due to electrostatic adsorption in the electrostatic field induced by triboelectricity. It is found that the ammonia‐sensitive material obtained by loading Ti3C2Tx in PFOTES‐CNF has a fast response/recovery (12/14 s), high sensitivity response (Vair/Vgas = 2.1), high selectivity response (37.6%), and low detection limit (10 ppm) for 100 ppm of ammonia gas. In addition, the ammonia‐sensitive CNF‐based triboelectric material can accurately identify NH3 concentration changes in the range of 10–120 ppm and transmit the signal wirelessly to the user interface, facilitating real‐time online monitoring of NH3 in the environment. A novel strategy is provided here for designing and preparing high‐performance gas‐sensitive composites and the analysis of self‐powered gas sensing is guided. [ABSTRACT FROM AUTHOR]

Though visualizing perspiration constituents is crucial for physiological evaluation, inadequate material healing and unreliable power supply methods restrict its applications. Herein, a fully flexible self‐powered sweat sensor is fabricated from a cellulose‐based conductive hydrogel to address these issues. The hydrogel electrode is composed of a cellulose nanocomposite polymerized in situ with polyaniline and cross‐linked with polyvinyl alcohol/borax. The cellulose nanocomposites furnish the sweat sensor with tensile and electrical self‐healing efficiencies exceeding 95% within 10 s, a stretchability of 1530%, and conductivity of 0.6 S m−1. The sweat sensor quantitatively analyzes Na+, K+, and Ca2+ contents in perspiration, to sensitivities of 0.039, 0.082, and 0.069 mmol–1, respectively, in real time via triboelectric effect and wirelessly transmits the results to a user interface. This fabricated sweat sensor with high flexibility, stability, and analytical sensitivity and selectivity provides new opportunities for self‐powered health monitoring. [ABSTRACT FROM AUTHOR]