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Contact electrification (triboelectrification) (CE) is a universal phenomenon in ambient environment and has been recorded for more than 2600 years. Nonetheless, the intrinsic mechanism of CE still remains controversial. Herein, based on first‐principles theory, the underlying mechanism in CE is systematically investigated between metallic MXenes and semiconductive MoS2. The results show that the work functions of contacting materials dominate the direction of electron transfer during CE process. That is, the electron will be transferred from the material with low work function to the one with high work function. The theoretical prediction is verified experimentally through investigating triboelectric probes based on MXenes and MoS2 nanomaterials. Additionally, it is noted that the interfacial potential barrier and the work function difference together modulate the amount of transferred electron. Electron transfer mainly occurs in the repulsive forces region where the interaction distance between the two materials is shorter than the normal bonding length. The quantum calculation results agree well with the Wang transition theory. Furthermore, it is also noticed that, due to the wave‐particle duality of electron, electron transfer will obviously occur at the attractive force region when the two contacting materials exhibit a larger work function difference. [ABSTRACT FROM AUTHOR]

Profited from the rapid development of flexible skin‐like electronic materials and artificial intelligent technology, remarkable achievements have been witnessed in wearable health monitoring devices in recent years. The wearable intelligent systems featured with tailored structures and compositions as well as enriched functions enable human beings to access to next‐generation closed‐loop platform for early disease prevention and diagnosis. In this context, this mini‐review focuses on the recent progress and applications of flexible wearable intelligent health monitoring devices. Specifically, the basic sensing mechanisms and corresponding property requirements for wearable healthcare devices are examined firstly. Secondly, the versatile applications of advanced wearable devices for detecting temperature, heart rate, blood pressure and glucose are scrutinized exclusively. Finally, a brief summary is presented accompanying with future outlook in terms of material preparation, mechanism development and integration design of monitoring systems. This manuscript is expected to provide critical guidelines to those working in skin‐like electronics, flexible sensors, wearable intelligent devices, health monitoring and other related disciplines, especially for the beginners. [ABSTRACT FROM AUTHOR]

Mass transfer is an essential factor determining photocatalytic performance, which can be modulated by fluid field via manipulating the kinetic characteristics of photocatalysts and photocatalytic intermediates. Past decades have witnessed the efforts and achievements made in manipulating mass transfer based on photocatalyst structure and composition design, and thus, a critical survey that scrutinizes the recent progress in this topic is urgently necessitated. This review examines the basic principles of how mass transfer behavior impacts photocatalytic activity accompanying with the discussion on theoretical simulation calculation including fluid flow speed and pattern. Meanwhile, newly emerged viable photocatalytic micro/nanomotors with self‐thermophoresis, self‐diffusiophoresis, and bubble‐propulsion mechanisms as well as magnet‐actuated photocatalytic artificial cilia for facilitating mass transfer will be covered. Furthermore, their applications in photocatalytic hydrogen evolution, carbon dioxide reduction, organic pollution degradation, bacteria disinfection and so forth are scrutinized. Finally, a brief summary and future outlook are presented, providing a viable guideline to those working in photocatalysis, mass transfer, and other related fields. [ABSTRACT FROM AUTHOR]

2D van der Waals (vdWs) heterostructure photodetectors have captured significant interest for their ability to achieve substantial optical conductivity gain and device tunability. However, the light absorption in ultrathin 2D inorganic vdWs devices is generally weak that leads to low detectivity. In addition, the intrinsic defects in 2D semiconductors cause significant carrier trapping and scattering by defect states during the transport process, which seriously restricts the response speed of the device. In this paper, a molybdenum tungsten disulfide (Mo0.1W0.9S2) is used to replace the conventional 2D semiconductor, while the light absorption efficiency of the device is significantly enhanced by the adoption of N’‐ Dimethyl‐3,4,9,10‐perylenedicarboximide (Me‐PTCDI), thus achieving both fast response and high detectivity. A series of type‐II organic/inorganic hybrid vdWs heterostructure photodetectors is systematically investigated based on Me‐PTCDI and Mo0.1W0.9S2. In particular, the device incorporating monolayer (ML) Me‐PTCDI and few‐layer (FL) Mo0.1W0.9S2 demonstrates a detectivity of up to 4.4 × 1011 Jones and a response time of 24.9 µs. By utilizing the device as a light sensing pixel, a single‐detecting pixel imaging system is demonstrated with high precision, showcasing promising prospects in fast imaging applications. [ABSTRACT FROM AUTHOR]