Submitted:
13 October 2025
Posted:
14 October 2025
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Abstract
Keywords:
1. Introduction
2. Desalination Technologies
2.1. Established Processes
2.1.1. Multi-Effect Distillation (MED)
2.1.2. Multi-Stage Flash (MSF)
2.1.3. Electrodialysis (ED)
2.1.4. Mechanical Vapor Compression (MVC)
2.1.5. Reverse Osmosis (RO)
2.2. Emerging Processes
2.2.1. Graphene-Oxide (GO)
2.2.2. Shock Electrodialysis (SED)
2.2.3. Forward Osmosis (FO)
2.3. RES-Powered Desalination Systems
3. Electrochemical Energy Storages
3.1. Lead-Acid Batteries
- Flooded (Vented) Lead-Acid (FLA): The traditional design where the electrolyte is in liquid form and requires periodic maintenance (topping up with distilled water) to compensate for water loss due to electrolysis and evaporation [60]. They are robust and low-cost but require ventilation due to gas emission during charging.
- Valve-Regulated Lead-Acid (VRLA): Sealed batteries that recombine internally generated gases, eliminating the need for watering.
- Absorbent Glass Mat (AGM): Uses a fiberglass mat to absorb the electrolyte, making it spill-proof, resistant to vibration, and capable of delivering high currents. It has a low self-discharge rate and is suitable for applications requiring reliability with minimal maintenance.
- Gel: The electrolyte is gelled with silica, which immobilizes it. These batteries are highly resistant to shock, vibration, and deep discharges, and have a very low self-discharge rate. However, they are sensitive to overcharging and require careful charge voltage control.
3.2. Lithium-Ion Batteries
- Lithium Titanate Oxide (LTO): Represents a unique lithium-ion chemistry that replaces the traditional graphite anode with one made of lithium titanate. This fundamental change grants LTO exceptional advantages, most notably extremely fast charging, a very long cycle life, and superior safety due to its high thermal stability and elimination of lithium plating [64]. However, these benefits come at the cost of lower energy density and a higher upfront cost compared to NMC or LFP batteries. LTO is ideally suited for applications where reliability, rapid cycling, and safety are paramount, such as in public transportation buses, and grid frequency regulation.
- Lithium Nickel Manganese Cobalt Oxide (NMC): Offers a balance of energy density, cycle life, and cost. Its cathode blends nickel, manganese, and cobalt, offering greater stability and longer cycle life than NCA variants, though at a slightly lower energy density [65]. NMC batteries are prevalent in electric vehicles, power tools, and renewable energy storage due to their reliability. Widely used in medium- to large-scale energy storage.
- Lithium Nickel Cobalt Aluminum Oxide (NCA): High specific energy and good longevity but requires careful thermal management. Its cathode combines nickel for reversibility, cobalt for stability, and aluminum to reduce structural stress during cycling. NCA batteries offer high energy and power density, making them suitable for electric vehicles and power tools [66]. Common in grid storage and automotive applications.
- Lithium Iron Phosphate (LFP): Distinguished by its exceptional safety, long cycle life, and stability. Though lower in energy density than NMC or NCA, its operational safety and durability is high [67]. These batteries are particularly well-suited for renewable energy-powered RO desalination due to their safety, long cycle life, and cost-effectiveness. Their superior thermal stability reduces fire risk, a critical advantage in remote or arid locations, while their ability to endure frequent charging and discharging aligns perfectly with solar or wind intermittency. Although LFP has a lower energy density than NMC, resulting in larger battery banks, this is often an acceptable trade-off for stationary RO applications where space is less constrained than in vehicles, Figure 4. The technology’s main limitations, reduced performance in cold climates and difficulties in state-of-charge estimation due to its flat voltage curve, can be mitigated with proper system design, insulation, and advanced battery management software. For these reasons, LFP has become the leading storage choice for sustainable, off-grid, and hybrid-powered RO desalination systems.
4. Fuel Cell Technologies
4.1. Fuel Cell Role in Renewable-Powered Desalination
4.2. Fundamentals and Design Aspects Relevant to Coastal Plants
4.3. Technology Families and Their Fit for Desalination Duty
- Alkaline fuel cells (AFCs) use an aqueous alkaline electrolyte, typically potassium hydroxide. Hydroxide ions move from the cathode to the anode; at the anode, hydrogen reacts with OH⁻ to form water and electrons, and at the cathode oxygen combines with water and electrons to regenerate OH⁻. The operating temperature is modest, usually around 60–80 °C, which simplifies thermal management and enables quick starts. The major drawback is sensitivity to carbon dioxide: CO₂ in the air or in the fuel converts the electrolyte into carbonates and degrades performance. In a coastal, open-air setting that sensitivity is a serious design constraint unless CO₂ scrubbing is provided [72]. When CO₂ can be controlled and very fast starts are valuable, small, islanded RO plants with frequent on/off cycles are a typical case, AFCs can be effective. Recent anion-exchange membrane variants aim to reduce CO₂ uptake by replacing liquid KOH with a solid membrane, but these systems are less mature than polymer electrolyte fuel cells [73].
- Proton exchange membrane fuel cells (PEMFCs) employ a solid polymer electrolyte that conducts protons. At the anode, hydrogen splits into protons and electrons; protons cross the membrane and combine with oxygen at the cathode to form water. PEMFCs operate near 60–80 °C, with high-temperature formulations reaching around 120 °C [74]. They are compact, respond rapidly to load changes, and start readily from cold, which makes them a natural partner for battery-smoothed RO operation. They are not affected by CO₂ in air, but they require very clean hydrogen because the catalysts are sensitive to carbon monoxide, sulfur compounds, and ammonia. The heat they produce is low-grade but still useful for feed preheating or low-temperature tasks. In most small to medium hybrid plants that prioritize operational simplicity and frequent cycling, PEMFCs provide the best overall match [75].
- Phosphoric acid fuel cells (PAFCs) and sulfuric acid variants use liquid acids as electrolytes, so the charge carrier is also the proton, but the operating window moves up to roughly 150–200 °C. At these temperatures, the stack yields a steadier flow of medium-grade heat, which can be absorbed by membrane distillation units, thermal pretreatment, or space and water heating within the facility. PAFCs are designed for stationary baseload operation; they ramp and start more slowly than PEMFCs and have lower power density, while still requiring noble-metal catalysts. They tolerate some impurities better than PEMFCs but remain sensitive to carbon monoxide and sulfur, so fuel quality control is still necessary [76].
- Molten carbonate fuel cells (MCFCs) operate much hotter, generally between 600 and 700 °C. The electrolyte is a molten carbonate salt held in a ceramic matrix. The mobile ionic species is CO₃²⁻, which forms at the cathode by reacting oxygen with carbon dioxide. Because carbonate ions carry charge, the cathode requires a controlled supply of CO₂, which is usually recirculated from the anode exhaust. At the anode, hydrogen reacts with CO₃²⁻ to produce water, CO₂, and electrons [77]. High temperature brings several advantages: platinum is unnecessary, nickel-based electrodes are sufficient, and internal reforming of light hydrocarbons such as natural gas or biogas is possible. The penalty is dynamic, the stacks prefer long, steady campaigns and do not appreciate frequent start–stop cycles, and the balance of plant must handle hot salt environments and CO₂ logistics. Where the desalination complex is large and continuous and can make use of high-temperature heat, for example, by preheating feed to multi-effect distillation, driving mechanical vapor compression auxiliaries, or feeding bottoming cycles, MCFCs can deliver excellent overall efficiency [78].
- Solid oxide fuel cells (SOFCs) push the temperature envelope further. Their ceramic electrolytes, often yttria-stabilized zirconia, conduct oxide ions from cathode to anode. At the cathode, oxygen molecules accept electrons and become O²⁻; at the anode, hydrogen reacts with O²⁻ to form water and release electrons back to the circuit [79]. Operating temperatures from roughly 600 up to 1,000 °C allow internal reforming and flexible fueling with clean natural gas, hydrogen, or syngas, without noble metals [80]. Like MCFCs, SOFCs are not designed for frequent thermal cycling; they are most comfortable in steady baseload service [81]. The quality of the heat they produce is exceptionally high. In desalination hubs that combine RO with thermal processes, SOFCs unlock cogeneration layouts that use the electrical output for high-pressure pumps and the thermal output for multi-effect or multi-stage systems, absorption chillers, or district heating and cooling that shares infrastructure with the water plant.
4.4. Hybridization with Batteries and Power Electronics
4.5. Integration Challenges and Mitigations in Coastal Deployment
4.6. Choosing the Right Fuel Cell for the Application
5. Energy Management Strategies
5.1. Rule-Based Strategies
5.1.1. Fuzzy Logic
5.1.2. Filter-Based Power Splitting
5.1.3. Finite-/Multi-State Logic
5.1.4. GA-Tuned Fuzzy and Neuro-Fuzzy (ANFIS)
5.2. Optimization-Based Strategies
5.2.1. Equivalent Consumption Minimization Strategy (ECMS)
5.2.2. Dynamic Programming (DP)
5.2.3. Pontryagin’s Minimum Principle (PMP)
5.2.4. Model Predictive Control (MPC)
5.2.5. Convex/QP and Mixed-Integer Programming
5.2.6. Other Metaheuristics
5.2.7. Robust and Stochastic Optimization
5.2.8. Degradation-Aware Optimization
5.3. Learning-Based Strategies
5.3.1. Reinforcement Learning (RL)
5.3.2. Supervised Learning
5.4. Distributed and Cooperative Control
5.4.1. Consensus-Based Control
5.4.2. Distributed Optimization (ADMM)
5.4.3. Multi-Agent MPC
5.5. Selection Guidelines
6. Discussion
5. Conclusions
Author Contributions
Funding
Data Availability Statement
Conflicts of Interest
Abbreviations
| ADMM | Alternating Direction Method of Multipliers |
| AEM | Anion-Exchange Membranes |
| AFC | Alkaline Fuel Cells |
| AGM | Absorbent Glass Mat |
| ANFIS | Adaptive Network-based Fuzzy Inference Systems |
| ANN | Artificial Neural Network |
| BESS | Battery Energy Storage System |
| BHS | Battery–Hydrogen Storage |
| CEM | Cation-Exchange Membranes |
| DC | Direct Current |
| DE | Differential Evolution |
| DoD | Depth of Discharge |
| DP | Dynamic Programming |
| ECMS | Equivalent Consumption Minimization Strategy |
| ED | Electrodialysis |
| EDR | Electrodialysis Reversal |
| EMS | Energy Management System |
| ERD | Energy Recovery Devices |
| ESS | Energy Storage System |
| FC | Fuel Cell |
| FLA | Flooded Lead-Acid |
| FLC | Fuzzy Logic Control |
| FO | Forward Osmosis |
| GO | Graphene-Oxide |
| HESS | Hybrid Energy Storage System |
| ICP | Ion Concentration Polarization |
| LFP | Lithium Iron Phosphate |
| LTO | Lithium Titanate Oxide |
| MCFC | Molten Carbonate Fuel Cells |
| MED | Multi-Effect Distillation |
| MG | Microgrid |
| MPC | Model Predictive Control |
| MSF | Multi-Stage Flash |
| MVC | Mechanical Vapor Compression |
| NCA | Nickel Cobalt Aluminum |
| NMC | Nickel Manganese Cobalt |
| PAFC | Phosphoric Acid Fuel Cells |
| PEMFC | Proton Exchange Membrane Fuel Cells |
| PID | Proportional-Integral-Derivative |
| PMP | Pontryagin’s Minimum Principle |
| PV | Photovoltaic |
| PSO | Particle Swarm Optimization |
| QPSO | Quantum Particle Swarm Optimization |
| RES | Renewable Energy Sources |
| RL | Reinforcement Learning |
| RO | Reverse Osmosis |
| SED | Shock Electrodialysis |
| SOC | State of Charge |
| SOFC | Solid Oxide Fuel Cells |
| SWRO | Seawater Reverse Osmosis |
| TVC | Thermal Vapor Compression |
| VFD | Variable Frequency Drives |
| VRLA | Valve-Regulated Lead-Acid |
| WT | Wind Turbine |
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| Technology | Energy type | Advantages | Disadvantages | Cost/m3 |
|---|---|---|---|---|
| MED | Therma, Electrical | High efficiency, operates at lower temperatures, good for cogeneration | High capital cost, complex construction, corrosion and scaling concerns | $0.8 - $2.5 |
| MSF | Thermal, Electrical | Reliable, robust, handles poor feedwater quality, large capacity | Very high energy consumption, high operating temperature promotes scaling | $1.0 - $3.0 |
| ED | Electrochemical | Highly efficient for brackish water, low pressure operation, high water recovery | Not suitable for seawater, membrane cost and replacement, pre-treatment required | $0.4 - $1.0 |
| MVC | Thermal | All thermal energy from electrical input, compact, modular, good for remote areas | Limited to small-to-medium scale, high electrical consumption, high maintenance costs | $1.5 - $3.0 |
| RO | Electrical | Lowest energy consumption (for membranes), modular, widespread, lower capital cost | Extensive pre-treatment required, membrane fouling and replacement, brine management | $0.5 - $1.5 |
| GO | Electrical | Potential for very high permeability and selectivity, potential for lower energy, antifouling properties | Early R&D stage, challenges with scalability, long-term stability in water, and membrane swelling | - |
| SED | Electrical | Membrane-less (avoids fouling/scaling), potential for high recovery rates and treatment of challenging feeds | Early R&D conceptual stage, challenges in scaling up from microfluidics, system complexity | - |
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