RESUMEN
Osmotic energy, as a renewable clean energy with huge energy density and stable yield, has received widespread attention over the past decades. Reverse electrodialysis (RED) based on ion-exchange membranes is an important method of obtaining osmotic energy from salinity gradients. The preparation of ion-exchange membranes with both high ion selectivity and ion permeability is in constant exploration. In this work, metal hydroxide-organic framework (MHOF) membranes are successfully prepared onto porous anodic aluminum oxide (AAO) membranes by a facile hydrothermal method to form Ni2(OH)2@AAO composite membranes, used for osmotic energy conversion. The surface is negatively charged with cation selectivity, and the asymmetric structure and extreme hydrophilicity enhance the ionic flux for effective capture of osmotic energy. The maximum output power density of 5.65 W m-2 at a 50-fold KCl concentration gradient is achieved, which exceeds the commercial benchmark of 5 W m-2. Meanwhile, the composite membrane can also show good performance in different electrolyte solutions and acid-base environments. This work provides a new avenue for the construction and application of MHOF membranes in efficient osmotic energy conversion.
RESUMEN
Sodium-ion batteries (SIBs) have garnered significant attention due to their potential as an emerging energy storage solution. Tin sulfide (SnS) has emerged as a promising anode material for SIBs due to its impressive theoretical specific capacity of 1022 mA h g-1 and excellent electrical conductivity. However, its practical application has been hindered by issues such as large volume expansion, which adversely affects cycling stability and rate performance during the charge/discharge processes. In this study, a novel approach to address these issues by synthesizing the bean pod cube hollow metal-organic framework (MOF)-SnSx/NC@N-doped carbon nanofibers through a process involving electrospinning, PDA coating, and calcination. The Sn-MOF serves as a self-sacrificing template, facilitating the simultaneous dissociation of MOF and polymerization of dopamine, leading to the creation of hollow intermediates that retain tin components. Subsequent sulfidation results in the integration of the hollow MOF-SnSx/NC nanoparticles within 3D nitrogen-doped carbon nanofibers, forming the distinctive bean pod cube composite structure. This unique configuration effectively shortens the diffusion path and mitigates volume expansion for sodium ions, ultimately yielding an exceptional high rate performance of 130 mA h g-1 (10 A g-1) and an ultralong cycling performance of 328 mA h g-1 even after 3500 cycles (2 A g-1) as the anode for SIBs.
RESUMEN
As an emerging metal-organic framework (MOF) material in recent years, the MOF-303 membrane has shown great potential applications in seawater desalination, dehydration, and atmospheric water harvesting. Herein, we report on a dense and uniform MOF-303 membrane fabricated by a facile in situ hydrothermal synthesis approach in the presence of an anodized aluminum oxide (AAO) channel membrane acting as the only Al source and substrate. Interestingly, the MOF-303 isomer can be obtained due to an insufficient amount of organic ligand caused by the less hydrophilic and larger pore size of the AAO substrate. The MOF-based composite membranes possessed surface-charge-governed ionic transport behavior. Moreover, the MOF-303/AAO membrane yielded an output power density of 1.87 W/m2 under a 50-fold KCl concentration gradient. Under a 50-fold gradient of artificial seawater and river water, a maximum power density of 1.46 W/m2 can be obtained. After 30 days of stability testing, the composite membrane still maintained the power output, and the power density was higher than 1.20 W/m2. This work provides a facile and effective strategy for constructing Al-based MOF composite membranes and boosts their applications in harvesting salinity-gradient energy.