Osmotic energy, often referred to as \"blue energy\", is the energy generated from the mixing of solutions with different salt concentrations, offering a vast, renewable, and environmentally friendly energy resource. The efficacy of osmotic power production considerably relies on the performance of the transmembrane process, which depends on ionic conductivity and the capability to differentiate between positive and negative ions. Recent advancements have led to the development of membrane materials featuring precisely tailored ion transport nanochannels, enabling high-efficiency osmotic energy harvesting. In this review, ion diffusion in confined nanochannels and the rational design and optimization of membrane architecture are explored. Furthermore, structural optimization of the membrane to mitigate transport resistance and the concentration polarization effect for enhancing osmotic energy harvesting is highlighted. Finally, an outlook on the challenges that lie ahead is provided, and the potential applications of osmotic energy conversion are outlined. This review offers a comprehensive viewpoint on the evolving prospects of osmotic energy conversion.

As promising prospects for renewable power harvesting, two-dimensional (2D) nanochannels for osmotic energy capture in a reverse electrodialysis arrangement have garnered significant attention. However, existing 2D nanochannel membranes have shown limited power generation capabilities due to challenges in balancing ion flux and selectivity. Here, we construct montmorillonite (MMT)/TEMPO-mediated oxidation cellulose nanofibers (TOCNFs) nanocomposite membranes for enhanced ion transmembrane transport. The intercalation of TOCNFs not only enlarges the interlayer distance, but also provides abundant space charge inside the nanochannels. Benefiting from the strong ion selectivity and high ion flux, the composite membrane achieves a remarkable power output of ∼16.57 W/m2 in the gradient of artificial seawater and river water, exceeding that of the state-of-the-art heterogeneous membrane-based osmotic energy conversion systems. Both experimental and theoretical findings confirm that the synergism of space and surface charge plays a crucial role in promoting osmotic energy conversion. This research contributes valuable insights into the optimization of 2D membranes for efficient clean energy harvesting purposes.

Osmotic energy harvesting was a promising way to alleviate energy crisis with reverse electrodialysis (RED) membrane-based technology. Charged hydrogel combined with other materials was an effective strategy to overcome problems, including restricted functional groups and complicated fabrication, but the effect of the respective charges of the two materials combined on the membrane properties has rarely been studied in depth. Herein, a new method was proposed that charged hydrogel was equipped with charged filter paper to form dual network fiber-hydrogel membrane for osmotic energy harvesting, which had excellent ion selectivity (beyond 0.9 under high concentration gradient), high ion transference number and energy conversion efficiency (beyond 32.5% under wide range concentration gradient), good property of osmotic energy conversion (∼4.84 W/m2 under 50-fold KCl and ∼6.75 W/m2 under simulated sea water and river water). Moreover, the power density was attributed to the surface-space charge synergistic effect from large amounts overlapping of electric double layer (EDL), so that the transmembrane ion transport was enhanced. It might be a valid mode to extensively develop the osmotic energy harvesting.

The massive reserves of osmotic energy existing in estuary will be highly desired as promising energy source that avails to solve the problem of energy shortage and environment deterioration. The ion transport membrane is core component optimized through composite membrane heterostructure to maximize the osmotic energy harvesting but suffer from gaps and resistance increase, which limit their practical applications. Here we demonstrate mono-component heterogeneous regenerated bacterial cellulose (RBC) membranes fabricated by subtle regenerated technique through Ionic Liquids (ILs). Such membranes obtain heterogeneous nature by the difference in fiber intertwining states due to the different treatment conditions on both sides. It achieves osmotic energy conversion with maximum power density of 0.70 W·m-2at 100-fold, which provides ingenious strategy for excellent performance and low-cost osmotic energy harvesting. By minimizing pores and maximizing the surface charges, energy barriers can be lowered, ion permeable and selective transport channels for energy harvesting device can be increased, as supported by the numerical simulation. This is the first time the construction strategy for mono-component heterogeneous membrane mediated by ILs for osmotic energy harvesting is proposed, which averts gaps between the layers of different materials effectively and provides theoretical guidance for subsequent in-depth research on mono-component ion-selective heterogeneous membrane.

Membrane-based salinity gradient energy generation from the osmotic potential at the interface of a river and seawater through reverse electrodialysis is a promising route for realizing clean, abundant, and sustainable energy. Membrane permeability and selective ion transport are crucial for efficient osmotic energy harvesting. However, balancing these two parameters in the membrane design and synthesis remains challenging. Herein, a hybridized bilayer metal-organic frameworks (MOF-on-MOF) membrane is fabricated for efficient transmembrane conductance for enhanced osmotic power generation. The heterogeneous membrane is constructed from imidazolate framework-8 (ZIF-8) deposited on a UiO-66-NH2 membrane intercalated with poly(sodium-4-styrenesulfonate) (PSS). The angstrom-scale cavities in the ZIF-8 layer promote ion selectivity by size exclusion, and the PSS-intercalated UiO-66-NH2 film ensures cation permeability. The synergistic effect is a simultaneous improvement in ion transport and selectivity from an overlapped electric double layer generating 40.01 W/m2 and 665 A/m2 permeability from a 500-fold concentration gradient interface at 3 KΩ and 9.20 W/m2 from mixing of real sea-river water. This work demonstrates a rational design strategy for hybrid membranes with improved ion selectivity and permeability for the water-energy nexus.

The unique ion-transport properties in nanoconfined pores enable nanofluidic devices with great potential in harvesting osmotic energy. The energy conversion performance could be significantly improved by the precise regulation of the \"permeability-selectivity\" trade-off and the ion concentration polarization effect. Here, we take the advantage of electrodeposition technique to fabricate a Janus metal-organic framework (J-MOF) membrane that possesses rapid ion-transport capability and impeccable ion selectivity. The asymmetric structure and asymmetric surface charge distribution of the J-MOF device can suppress the ion concentration polarization effect and enhance the ion charge separation, exhibiting an improved energy harvesting performance. An output power density of 3.44 W/m2 has been achieved with the J-MOF membrane at a 1000-fold concentration gradient. This work provides a new strategy for fabricating high-performance energy-harvesting devices.

Batch pressure-retarded osmosis (PRO) with varied-pressure and multiple-cycle operation using a pressurized variable-volume tank has been proposed as a high-efficiency osmotic energy harvesting technology, but it suffers scalability constraints. In this study, a more scalable batch PRO, namely, atmospheric batch PRO (AB-PRO), was proposed, utilizing an atmospheric tank to receive and store the intermediate diluted draw solution (DS) and a pressure exchanger to recover the pressure energy from the diluted DS before being recycled into the tank. Its performance was further compared with single-stage PRO (SS-PRO) at different flow schemes via analytic models. The results show that the AB-PRO with an infinitesimal per-cycle water recovery (r) approaches the thermodynamic maximum energy production under ideal conditions, outperforming the SS-PRO with lower efficiencies caused by under-pressurization (UP). However, when considering inefficiencies, a ~40% efficiency reduction was observed in AB-PRO owing to UP and entropy generation as the optimal r is no-longer infinitesimal. Nonetheless, AB-PRO is still significantly superior to SS-PRO at low water recoveries (R) and maintains a stable energy efficiency at various R, which is conducive to meeting the fluctuating demand in practice by flexibly adjusting R. Further mitigating pressure losses and deficiencies of energy recovery devices can significantly improve AB-PRO performance.

Biological ion channels existing in organisms are critical for many biological processes. Inspired by biological ion channels, the heterogeneous electrospinning nanofiber membranes (HENM) with functional ion channels are constructed by electrospinning technology. The HENM successfully realizes ion-gating effects, which can be used for tunable energy conversions. Introduction of pyridine and carboxylic acid groups into the HENM plays an important role in generating unique and stable ion transport behaviors, in which gates become alternative states of open and close, responding to symmetric/asymmetric pH stimulations. Then we used the HENM to convert osmotic energy into electric energy which reach a maximum value up to 12.34 W m-2 and the output power density of HENM-based system could be regulated by ion-gating effects. The properties of the HENM provide widespread potentials in application of smart nanofluidic devices, energy conversion, and water treatment.

Inspired by acute temperature sensors in the mammalian sensory system to seek comfortable living environment, we construct temperature sensing nanochannels that are tightly linked to photo gating to form photothermal controlled nanochannels membrane. This membrane arises from the composite of laminar regenerated cellulose (RC) membrane formed by dissolution and regeneration of cellulose in the novel superbase-derived ionic liquid and poly-l-lysine (PLL)-modified conical nanochannels polyethylene terephthalate (PET) substrate. Fe3O4 nanoparticles are introduced into RC membrane as gating modifiers, controlling ion flux and osmotic energy conversion. Nanochannels are activated upon photo, inducing temperature changes result in PLL molecule structure shifted from α-helix to β-sheet. The difference in the rectification ratio at different temperatures is associated with photothermal-dependent opening and closing, its maximum is 116.76. This system could deliver an output power of approximately 4.9 W/m2 in osmotic energy harvesting. Our results suggest a simple photothermal-gating ion transport principle in laminar RC membrane.

A vast amount of energy can be extracted from the untapped low-grade heat from sources below 100 °C and the Gibbs free energy from salinity gradients. Therefore, a process for simultaneous and direct conversion of these energies into electricity using permselective membranes was developed in this study. These membranes screen charges of ion flux driven by the combined salinity and temperature gradients to achieve thermo-osmotic energy conversion. Increasing the charge density in the pore channels enhanced the permselectivity and ion conductance, leading to a larger osmotic voltage and current. A 14-fold increase in power density was achieved by adjusting the ionic site population of covalent organic framework (COF) membranes. The optimal COF membrane was operated under simulated estuary conditions at a temperature difference of 60 K, which yielded a power density of ≈231 W m-2 , placing it among the best performing upscaled membranes. The developed system can pave the way to the utilization of the enormous supply of untapped osmotic power and low-grade heat energy, indicating the tremendous potential of using COF membranes for energy conversion applications.