Owing to its 100% theoretical salt rejection capability, membrane distillation (MD) has emerged as a promising seawater desalination approach to address freshwater scarcity. Ideal MD requires high vapor permeate flux established by cross-membrane temperature gradient (∆T) and excellent membrane durability. However, it’s difficult to maintain constant ∆T owing to inherent heat loss at feedwater side resulting from continuous water-to-vapor transition and prevent wetting transition-induced membrane fouling and scaling. Here, we develop a Ti3C2Tx MXene-engineered membrane that imparts efficient localized photothermal effect and strong water-repellency, achieving significant boost in freshwater production rate and stability. In addition to photothermal effect that circumvents heat loss, high electrically conductive Ti3C2Tx MXene also allows for self-assembly of uniform hierarchical polymeric nanospheres on its surface via electrostatic spraying, transforming intrinsic hydrophilicity into superhydrophobicity. This interfacial engineering renders energy-efficient and hypersaline-stable photothermal membrane distillation with a high water production rate under one sun irradiation.

Photothermal desalination is a promising approach for seawater purification by harvesting solar energy. Titanium carbide (Ti 3 C 2 T x MXene) membranes have been regarded as potential materials for photothermal desalination by virtue of their excellent light-to-heat conversion. However, achieving a well-balanced synergy between high evaporation rate and good salt resistance remains a significant challenge due to their limited solar absorption and inferior stability. Herein, we report a self-assembled flexible porphyrin-Ti 3 C 2 T x MXene Janus membrane (Janus PMX membrane) for dual-functional enabled photothermal desalination. The self-assembly of porphyrin on MXene not only effectively creates a favorable hydrophobic surface but also simultaneously enables efficient solar utilization. The significant interactions and charge redistribution between MXene and porphyrin lead to a stable hydrophobic/hydrophilic Janus structure with synergistically enhanced photothermal conversion. As a result, the Janus PMX membrane demonstrates highly efficient water pumping, heat localization, vapor generation, and salt resistance during photothermal desalination. This work presents an effective and facile strategy toward advancing a well-performing MXene membrane for efficient seawater desalination.

No abstract

Manipulating liquid is of great significance in fields from life sciences to industrial applications. Owing to its advantages in manipulating liquids with high precision and flexibility, electrowetting on dielectric (EWOD) has been widely used in various applications. Despite this, its efficient operation generally needs electrode arrays and sophisticated circuit control. Here, we develop a largely unexplored triboelectric wetting (TEW) phenomenon that can directly exploit the triboelectric charges to achieve the programmed and precise water droplet control. This key feature lies in the rational design of a chemical molecular layer that can generate and store triboelectric charges through agile triboelectrification. The TEW eliminates the requirement of the electric circuit design and additional source input and allows for manipulating liquids of various compositions, volumes, and arrays on various substrates in a controllable manner. This previously unexplored wetting mechanism and control strategy will find diverse applications ranging from controllable chemical reactions to surface defogging.

No abstract

MgH nanoparticles (NPs) uniformly anchored on graphene (GR) are fabricated based on a bottom-up self-assembly strategy as anode materials for lithium-ion batteries (LIBs). Monodisperse MgH NPs with an average particle size of ∼13.8 nm are self-assembled on the flexible GR, forming interleaved MgH/GR (GMH) composite architectures. Such nanoarchitecture could effectively constrain the aggregation of active materials, buffer the strain of volume changes, and facilitate the electron/lithium ion transfer of the whole electrode, leading to a significant enhancement of the lithium storage capacity of the GMH composite. Furthermore, the performances of GMH composite as anode materials for LIBs are enabled largely through robust interfacial interactions with poly(methyl methacrylate) (PMMA) binder, which plays multifunctional roles in forming a favorable solid-electrolyte interphase (SEI) film, alleviating the volume expansion and detachment of active materials, and maintaining the structural integrity of the whole electrode. As a result, these synergistic effects endow the obtained GMH composite with a significantly enhanced reversible capacity and cyclability as well as a good rate capability. The GMH composite with 50 wt % MgH delivers a high reversible capacity of 946 mA h g at 100 mA g after 100 cycles and a capacity of 395 mAh g at a high current density of 2000 mA g after 1000 cycles.

Magnesium sulfide (MgS), representative of alkaline-earth metal chalcogenides (AEMCs), is a potential conversion/alloy-type electrode material for lithium ion batteries (LIBs), by virtue of its low potential, high theoretical capacity, and abundant magnesium resource. However, the limited capacity utilization and inferior rate performance still hinder its practical application, and the progress is rather slow due to the challenging fabrication technique for MgS. Herein, we report a series of controlledsize hollow MgS nanocrystals (NCs) homogeneously distributed on graphene (MgS@G), fabricated through a metal hydride framework (MHF) strategy, and its application as advanced electrode material for LIBs. The hollow structure of MgS NCs is mainly attributed to the Kirkendall effect and the escape of hydrogen atoms from metal hydride during sulfuration. The as-synthesized MgS@G demonstrates robust nanoarchitecture and admirable interactions, which ensure a spatially confined lithiation/delithiation process, optimize the dynamics of two-steps conversion/alloying reactions, and induce a synergetic pseudocapacitive storage contribution. As a result, a representative MgS@G composite delivers a largely enhanced capacity of >1208 mAh g −1 at a current density of 100 mA g −1 and a long-term cycle stability at a high current density of 5 A g −1 with a capacity of 838 mAh g −1 over 3000 cycles, indicating well-sustained structural integrity. This work presents an effective route toward the development of high-performance magnesium-based material for energy storage.

Metal hydrides have attracted great intentions as anodes for lithium-ion batteries (LIBs) due to their extraordinary theoretical capacity. It is an unsolved challenge, however, to achieve high capacity with stable cyclability, owing to their insulating property and large volume expansion upon lithium storage. Here, we introduce self-initiated polymerization to realize molecular-scale functionality of metal hydrides with conductive polymer, that is, polythiophene (PTh), on graphene, leading to the formation of MgH2@PTh core−shell nanoparticles on graphene. The nanoscale characteristics of MgH2 not only relieve the induced stress upon volume changes but also allow fast diffusivity and high reactivity for Li-ion transport. More importantly, the conformal coating of ultrathin PTh membrane can effectively suppress the detrimental reactions between MgH2 and electrolyte, provide enhanced performance with facile electron and Li+ transport, and preserve its structural integrity, attributed to the strong molecular interaction between PTh and MgH2 as well as its various products during electrochemical reactions. With this structure, a high reversible specific capacity of 1311 mAh g−1 at 100 mA g−1, excellent rate performance of 1025 mAh g−1 at 2000 mA g−1, and a capacity retention of 84.5% at 2000 mA g−1 after 500 cycles are observed for MgH2@PTh nanoparticles as anode for LIBs.