Direct electricity generation from water flow/evaporation, coined hydrovoltaic effect, has recently attracted intense interest as a facile approach to harvest green energy from ubiquitous capillary water flow or evaporation. However, the current hydrovoltaic device is inferior in output power efficiency compared to other renewable energy devices. Slow water evaporation rate and inefficient charge collection at device electrodes are two fundamental drawbacks limiting energy output efficiency. Here, we report a bioinspired hierarchical porous fabric electrode that enables high water evaporation rate, efficient charge collection, and rapid charge transport in nanostructured silicon-based hydrovoltaic devices. Such an electrode can efficiently collect charges generated in nanostructured silicon as well as induce a prompt water evaporation rate. At room temperature, the device can generate an open-circuit voltage (V oc) of 550 mV and a short-current density (J sc) of 22 μA·cm–2. It can output a power density over 10 μW·cm–2, which is 3 orders of magnitude larger than all those reported for analogous hydrovoltaic devices. Our results could supply an effective strategy for the development of high-performance hydrovoltaic devices through optimizing electrode structures.

Inkjet printing is a powerful technology for realizing high‐density pixelated perovskite light‐emitting diodes (PeLEDs). However, the coffee‐stain effect in the inkjet printing process often leads to uneven thickness and poor crystallization of printed perovskite features, which deteriorates the performance of PeLEDs. Here, a strategy is developed to suppress the coffee‐stain effect via enhancing Marangoni flow strength. An interfacial poly(vinylpyrrolidone) (PVP) layer is incorporated to tune the surface tension of the underlying hole transport layer (HTL) and enhance the perovskite crystallization. The substrate temperature is also carefully controlled to tune the printing solvent evaporation rate rationally. By optimizing the thickness of the PVP layer and the temperature of the printing stage, the coffee‐stain effect is dramatically restrained. In addition, the interfacial insulating PVP layers play a positive role in suppressing leakage current level of PeLEDs by avoiding any direct electrical contact between HTL and electron transporting layer. Finally, an inkjet‐printed PeLED with a brightness of 3640 cd m–2 and external quantum efficiency of 9.0% is achieved. This work highlights the availability of inkjet‐printing technology for fabricating patterned PeLEDs in information display applications.

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Hydrovoltaic devices are proposed as an alternative way to directly generate electricity due to the ubiquity of water and its interaction with specific porous structures. At present, the output power density of the reported device is limited by its low current density arising from the low surface charge density and inferior charge transport capability of the active materials. In this work, an asymmetric structure consisting of positively charged conductive polyaniline (PANI) and negatively charged Ti 3 C 2 T X MXene is proposed to build a hydrovoltaic device to achieve high conductivity and surface charge density simultaneously. An extra polyvinyl alcohol layer is utilized between PANI and MXene to reserve the asymmetric structure and maintain a constant voltage output. As a result, a peak current density of 1.8 mA/cm 2 is achieved, which is 18 times higher than the previous peak current density of the device with an inert electrode. Our work of incorporating an asymmetric structure provides an alternative way to target highefficiency hydrovoltaic devices with a large current density.

In non‐fullerene‐based photovoltaic devices, it is unclear how excitons efficiently dissociate into charge carriers under small driving force. Here, we developed a modified method to estimate dielectric constants of PM6 donor and non‐fullerene acceptors. Surprisingly, most non‐fullerene acceptors and blend films showed higher dielectric constants. Moreover, they exhibited larger dielectric constants differences at the optical frequency. These results are likely bound to reduced exciton binding energy and bimolecular recombination. Besides, the overlap between the emission spectrum of donor and absorption spectra of non‐fullerene acceptors allowed the energy transfer from donor to acceptors. Hence, based on the synergistic effect of dielectric property and energy transfer resulting in efficient charge separation, our finding paves an alternative path to elucidate the physical working mechanism in non‐fullerene‐based photovoltaic devices.