Efficient utilization of solar energy for clean water is an attractive, renewable, and environment friendly way to solve the long-standing water crisis. For this task, we prepared the long-range vertically aligned graphene sheets membrane (VA-GSM) as the highly efficient solar thermal converter for generation of clean water. The VA-GSM was prepared by the antifreeze-assisted freezing technique we developed, which possessed the run-through channels facilitating the water transport, high light absorption capacity for excellent photothermal transduction, and the extraordinary stability in rigorous conditions. As a result, VA-GSM has achieved average water evaporation rates of 1.62 and 6.25 kg m h under 1 and 4 sun illumination with a superb solar thermal conversion efficiency of up to 86.5% and 94.2%, respectively, better than that of most carbon materials reported previously, which can efficiently produce the clean water from seawater, common wastewater, and even concentrated acid and/or alkali solutions.

Two-dimensional nanofluidic channels are emerging candidates for capturing osmotic energy from salinity gradients. However, present two-dimensional nanofluidic architectures are generally constructed by simple stacking of pristine nanosheets with insufficient charge densities, and exhibit low-efficiency transport dynamics, consequently resulting in undesirable power densities (<1 W m −2 ). Here we demonstrate MXene/Kevlar nanofiber composite membranes as high-performance nanofluidic osmotic power generators. By mixing river water and sea water, the power density can achieve a value of approximately 4.1 W m −2 , outperforming the state-of-art membranes to the best of our knowledge. Experiments and theoretical calculations reveal that the correlation between surface charge of MXene and space charge brought by nanofibers plays a key role in modulating ion diffusion and can synergistically contribute to such a considerable energy conversion performance. This work highlights the promise in the coupling of surface charge and space charge in nanoconfinement for energy conversion driven by chemical potential gradients.

Two‐dimensional (2D) titanium carbide (Ti3C2) is emerging as an important member of the MXene family. However, fluoride‐based synthetic procedures remain an impediment to the practical applications of this promising class of materials. Here we demonstrate an efficient fluoride‐free etching method based on the anodic corrosion of titanium aluminium carbide (Ti3AlC2) in a binary aqueous electrolyte. The dissolution of aluminium followed by in situ intercalation of ammonium hydroxide results in the extraction of carbide flakes (Ti3C2Tx, T=O, OH) with sizes up to 18.6 μm and high yield (over 90 %) of mono‐ and bilayers. All‐solid‐state supercapacitor based on exfoliated sheets exhibits high areal and volumetric capacitances of 220 mF cm−2 and 439 F cm−3, respectively, at a scan rate of 10 mV s−1, superior to those of LiF/HCl‐etched MXenes. Our strategy paves a safe way to the scalable synthesis and application of MXene materials.

Nowadays, the increasing requirements of portable, implantable, and wearable electronics have greatly stimulated the development of miniaturized energy storage devices (MESDs). Electrochemically active materials and microfabrication techniques are two indispensable parts in MESDs. Particularly, the architecture design of microelectrode arrays is beneficial to the accessibility of two-dimensional (2D) active materials. Therefore, this study reviews the recent advancements in microbatteries and microsupercapacitors based on electrochemically active 2D materials. Emerging microfabrication strategies enable the precise control over the thickness, homogeneity, structure, and dimension in miniaturized devices, which offer tremendous opportunities for achieving both high energy and power densities. Furthermore, smart functions and integrated systems are discussed in detail in light of the emergence of intelligent and interactive modes. Finally, future developments, opportunities, and urgent challenges related to 2D materials, device fabrications, smart responsive designs, and microdevice integrations are provided.

Hygroelectricity is proposed as a means to produce electric power from air by absorbing gaseous or vaporous water molecules, which are ubiquitous in the atmosphere. Here, using a synergy between a hygroscopic bulk graphene oxide with a heterogeneous structure and interface mediation between electrodes/materials with Schottky junctions, we develop a high-performance hygroelectric generator unit with an output voltage approaching 1.5 V. High voltage (e.g., 18 V with 15 units) can be easily reached by simply scaling up the number of hygroelectric generator units in series, enough to drive commercial electronic devices. This work provides insight for the design and development of hygroelectric generators that may promote the efficient conversion of potential energy in the environmental atmosphere to electricity for practical applications.