Energy Conversion Technologies Research Articles

Design of Multifunctional Electrocatalysts for ORR/OER/HER/HOR: Janus Makes Difference.

Multifunctional electrocatalysts for hydrogen evolution reaction (HER), hydrogen oxidation reaction (HOR), oxygen evolution reaction (OER), and oxygen reduction reaction (ORR) have broad application prospects; However, realization of such kinds of materials remain difficulties because it requires the materials to have not only unique electronic properties, but multiple active centers to deal with different reactions. Here, employing density functional theory (DFT) computations, it is demonstrated that by decorating the Janus-type 2D transition metal dichalcogenide (TMD) of TaSSe with the single atoms, the materials can achieve multifunctionality to catalyze the ORR/OER/HER/HOR. Out of sixteen catalytic systems, Pt-VS (i.e., Pt atom embedded in the sulfur vacancy), Pd-VSe, and Pt-VSe@TaSSe are promising multifunctional catalysts with superior stability. Among them, the Pt-VS@TaSSe catalyst exhibits the highest activity with theoretical overpotentials ηORR = 0.40V, ηOER = 0.39V, and ηHER/HOR = 0.07V, respectively, better than the traditional Pt (111), IrO2 (110). The interplays between the catalyst and the reaction intermediate over the course of the reaction are then systematically investigated. Generally, this study presents a viable approach for the design and development of advanced multifunctional electrocatalysts. It enriches the application of Janus, a new 2D material, in electrochemical energy storage and conversion technology.

Nanoscale-Confined Synthesis of 2D Metal Compounds for Electrochemical Applications.

2D metal compounds, such as transition metal dichalcogenides (TMDs), layered double hydroxides (LDHs), and MXenes, are emerging as important electrocatalyst materials in the transition to a sustainable energy future. Aided by their high surface area, electrical conductivity, and tunable electronic properties, these materials have provided a crucial research thrust in enhancing the efficiency of green hydrogen production, fuel cells, and carbon reduction processes. Most importantly, the synthesis of nanostructured 2D compounds, while challenging, is the key to optimizing their catalytic performance. Recent advancements in this field have highlighted the potential of 2D metal compounds in revolutionizing energy conversion technologies, which entails the discovery of new material compositions, the development of novel synthetic routes, and the integration of these materials into practical energy conversion systems. This review presents an overview of the distinctive characteristics of nanoscale-confined 2D metal compounds, the challenges encountered in their synthesis, and electrochemical applications.

Corrosion and Protection of Electrocatalysts toward Advanced Energy Technologies

AbstractHigh‐efficiency electrocatalysts play an important role in clean energy conversion technologies. Generally, electrocatalysts in different environments, including voltage, acid, and alkali electrolytes, are more susceptible to corrosion, which will induce structural and performance changes. Based on the latest achievements in the corrosion and protection of electrocatalysts in advanced energy technologies, this review mainly studies the application of various corrosion strategies to construct superior electrocatalysts, including chemical etching, metal corrosion transformation, and corrosion reconstruction, and their affecting factors are also appraised and summarized. To improve the stability of electrocatalysts, various corrosion inhibition strategies, such as carrier improvement and composition regulation accompanied by structure optimization, are reviewed. In addition, the application of catalyst corrosion in electrochemical energy technologies is examined from the perspective of the structure‐activity‐performance relationship. In the end, this article concludes the perspective and challenges of electrocatalyst corrosion in energy conversion and storage technologies. This article provides insights and directions for designing electrocatalysts with high efficiency and low corrosion, which is beneficial for developing corrosion chemistry for sustainable energy technologies.

Energy Bus-Based Matrix Modeling and Optimal Scheduling for Integrated Energy Systems

Integrated energy systems (IESs) can easily accommodate renewable energy resources (RESs) and improve the utilization efficiency of fossil energy by integrating various energy production, conversion, and storage technologies. However, the coupled multi-energy flows and the uncertainty of RESs bring challenges regarding optimal scheduling. Therefore, this study proposes an energy bus-based matrix-modeling method and a coordinated scheduling strategy for the IES. The matrix-modeling method can be used to formulate the steady- and transient-state balances of the multi-energy flows, and the transient model can clearly express the multi-time-scale characteristics of the different energy flows. The model parameters are fitted with data from experiments and the literature. To address the inherent randomness of the RESs and loads, a coordinated scheduling strategy is designed that contains two components: day-ahead optimization and rolling optimization. Day-ahead optimization uses the system steady-state model and multiple scenarios from the RES and load forecast data to minimize the operation cost while rolling optimization is based on the system’s transient-state model and aims to achieve the optimal real-time scheduling of the energy flows. Finally, a case study is conducted to verify the advantages and effectiveness of the proposed model and optimization method. The results show that stochastic optimization reduces the total daily cost by 1.48% compared to deterministic optimization when considering the prediction errors associated with the RESs and loads, highlighting the stronger adaptability of stochastic optimization to prediction errors. Moreover, rolling optimization based on the system’s transient-state model can reduce the errors between day-ahead scheduling and rolling correction.

IV‐VI/I‐V‐VI2 Thermoelectrics: Recent Progress and Perspectives

AbstractThermoelectric energy conversion technology is considered as one of the most promising solutions for recovering waste heat generated by fossil fuel combustion. As typical types of thermoelectric materials in the middle and high‐temperature range (500–900 K), binary IV‐VI (IV = Ge, Sn, Pb; VI = Se, Te) compounds are extensively studied. Lately, the obtained high‐performance thermoelectric solid solutions between IV‐VI and I‐V‐VI2 (I = Li, Na, K, Ag, Cu; V = Sb, Bi; VI = S, Se, Te) compounds have brought those complex chalcogenides back to the central point of thermoelectric community due to the emerging rich physical phenomena. Profiting from this effective approach, unveiling the underlying mechanism and understanding of alloying effect on the transport properties of these solid solutions becomes particularly significant. This review presents the latest progress in designing high‐performance IV‐VI/I‐V‐VI2 solid solutions and the underlining physical mechanisms, in which detailed discussion about the role of I‐V‐VI2 compounds play in optimizing individual properties of IV‐VI materials is made. This comprehensive review highlights the multiple effects of I‐V‐VI2 alloying on thermoelectric properties of IV‐VI compounds and will drive the related research interests aiming at developing new‐generation thermoelectric compounds in this family.

Development of Bio-Photoelectrochemical Hybrids for Solar Energy Conversion

Recent advancements in solar energy conversion have identified bio-photoelectrochemical hybrids as one of the most promising sustainable techniques. This study integrates BiVO4 and TiO2 semiconductors with photoautotrophic microorganisms (e.g., Algae) to enhance solar energy conversion. Thin films of these materials were prepared and characterized, revealing a relatively smooth surface for BiVO4 while structures for TiO2 thin films deposited as nanorods. Optical properties showed band gaps of ≤ 3.1 and 2.4 eV for TiO2 and BiVO4, respectively. The point of zero charge of materials was investigated, indicating that naturally occurring biofilm formation might not be favorable for as-prepared materials. To overcome this challenge, we aimed to use polyelectrolytes to enhance attachment of cells on the surface of semiconductor and in this regards we determined the biocompatibility of using this approach. Photoelectrochemical (PEC) measurements were conducted to evaluate solar energy conversion efficiency. This study offers insights into optimizing biosystem attachment, biofilm stability, and PEC performance of coupled semiconductors with photoautotrophic microorganisms as one photoelectrode in PEC cell, advancing sustainable solar energy conversion technologies.

Cerium-doped Nickel SulfideNanospheres as EfficientCatalysts for Overall Water Splitting.

The development of non-precious metal electrocatalysts with excellent activity and durability for electrochemical water splitting has always been a goal. Transition metal sulfides are attractive electrocatalysts for both hydrogen evolution reaction (HER) and oxygen evolution reaction(OER). In this article, we designed and constructed efficient catalysts with multiple synergistic interactions and synthesized Ce-NiS2@NFnanosphere using a solvothermal method. Ce-NiS2@NF exhibits excellent HER performance, OER performance, and overall water splitting capability in alkaline electrolytes, demonstrating good stability. The addition of Ce influences the activity of the catalysts, attributed to the synergistic interactions creating more active sites and higher intrinsic activity through the introduction of Ce heteroatoms. Additionally, the self-supported conductive substrate promotes electron transfer, enhancing the intrinsic activity and active site density of the catalyst.This study provides an in-depth investigation into structural design and performance enhancement, offering ideas for designing efficient catalysts for overall water electrolysis. This work provides an in-depth study in terms of structural design performance enhancement and provides ideas for designing efficient alkaline bifunctional catalysts. Valuable insights have been provided in elucidating the intrinsic mechanism of the catalytic activity of cerium-doped nickel sulfidenanospheres,thus providing new guidance in the field of energy conversion technology.

Superior Oxygen Evolution Electrocatalyst based on Ni‐Ellagic Acid Coordination Polymer

AbstractThe oxygen evolution reaction (OER) is central to energy conversion technologies, but the high cost and scarcity of commercial noble metal catalysts limit their widespread application. Natural products exhibit great potential in preparing high‐performance electrocatalysts due to their cost‐effectiveness and sustainability. Here, a kind of 1D polymers [M‐EA (M═Co, Cu, Ni)] for oxygen evolution reaction via the complexation of ellagic acid (EA) with metal ions are reported. It is found that Ni‐EA displays a low overpotential (190 mV at 10 mA cm−2) and an ultralow Tafel slope (28 mV dec−1), with a production cost of only 3.6 × 10−2% of IrO2. Density functional theory investigations reveal the electrocatalytic mechanism of the OER. A rechargeable Zn‐Air battery using Ni‐EA+Pt/C as the air electrode shows a lower charging potential and better cycling stability than the IrO2+Pt/C‐based battery. This work provides a train for the development of state‐of‐the‐art OER catalysts.

Design and cooling of permanent magnet generator in MW-class space closed Brayton cycle system

The closed Brayton cycle (CBC) system is a prime energy conversion technology to convert heat from the reactor to electric power for space missions due to its light weight, compact and stable operation. The CBC system incorporates a permanent magnet generator (PMG) mounted on the CBC shaft with the turbine and compressor. To ensure safe operation of the CBC system, a small fraction of the working fluid is used to provide the required cooling. In this study, four different cooling schemes used in CBC system are concluded and the key dimensions of the PMG are obtained through mechanical design theory and electromagnetic theory. Comprehensive research on the electromagnetic field and loss calculation is then performed. Furthermore, the cooling paths of the PMG are designed and the resulting temperature profiles are calculated. Finally, different cooling schemes are compared and the appropriate cooling advice is proposed.

The current state of transition metal-based electrocatalysts (oxides, alloys, POMs, and MOFs) for oxygen reduction, oxygen evolution, and hydrogen evolution reactions

Climate change is showing its impacts now more than ever. The intense use of fossil fuels and the resulting CO2 emissions are mainly to blame, accentuating the need to develop further the available energy conversion and storage technologies, which are regarded as effective solutions to maximize the use of intermittent renewable energy sources and reduce global CO2 emissions. This work comprehensively overviews the most recent progress and trends in the use of transition metal-based electrocatalysts for three crucial reactions in electrochemical energy conversion and storage, namely, the oxygen evolution (OER), oxygen reduction (ORR), and hydrogen evolution (HER) reactions. By analyzing the state-of-the-art polyoxometalates (POMs) and metal-organic frameworks (MOFs), the performance of these two promising types of materials for OER, ORR, and HER is compared to that of more traditional transition metal oxides and alloy-based electrocatalysts. Both catalytic activity and stability are highly influenced by the adsorption energies of the intermediate species formed in each reaction, which are very sensitive to changes in the microstructure and chemical microenvironment. POMs and MOFs allow these aspects to be easily modified to fine-tune the catalytic performances. Therefore, their chemical tunability and versatility make it possible to tailor such properties to obtain higher electrocatalytic activities, or even to obtain derived materials with more compelling properties towards these reactions.

Monitoring Ti3C2Tx MXene Degradation Pathways Using Raman Spectroscopy.

Extending applications of Ti3C2Tx MXene in nanocomposites and across fields of electronics, energy storage, energy conversion, and sensor technologies necessitates simple and efficient analytical methods. Raman spectroscopy is a critical tool for assessing MXene composites; however, high laser powers and temperatures can lead to the materials' deterioration during the analysis. Therefore, an in-depth understanding of MXene photothermal degradation and changes in its oxidation state is required, but no systematic studies have been reported. The primary aim of this study was to investigate the degradation of the MXene lattice through Raman spectroscopic analysis. Distinct spectral markers were related to structural alterations within the Ti3C2Tx material after subjecting it to thermal- and laser-induced degradation. During the degradation processes, spectral markers were revealed for several specific steps: a decrease in the number of interlayer water molecules, a decrease in the number of -OH groups, formation of C-C bonds, oxidation of the lattice, and formation of TiO2 nanoparticles (first anatase, followed by rutile). By tracking of position shifts and intensity changes for Ti3C2Tx, the spectral markers that signify the initiation of each step were found. This spectroscopic approach enhances our understanding of the degradation pathways of MXene, and facilitating enhanced and dependable integration of these materials into devices for diverse applications, from energy storage to sensors.

Single-atom Al precisely modulate the strain of Pt3Co intermetallic for superior oxygen catalytic performance

Precisely controlling the strain of Pt-based intermetallic to ensure high performance and stability is a massive task for sustainable proton-exchange-membrane-fuel-cells. Herein, the Al single-atom was trapped into the L12-Pt3Co intermetallic core to precisely tailor the strain state on the Pt-skin for fast oxygen reduction reaction kinetics. Theoretical calculations firstly predicted that only tailored tension can accelerate the protonation of O2 on L12-Pt3Co@Pt without creating an additional energy barrier for subsequent oxygen-containing intermediates desorption. Experimentally, Al single-atom confined in the L12-Pt3Co lattice by substituting partial Co occupancy, imposing tailored ∼ 0.2 % tension on Pt-skin compared to the L12-Pt3Co. L12-Al-Pt3Co@Pt/C exhibits enhanced mass activity which is ten-time improvement over commercial Pt/C. More significantly, XAS and DFT results reveal that the Al single-atom can strengthen the Pt-Co bonding, enhancing the stability of L12-Al-Pt3Co@Pt/C in oxygen reduction. This work provides an avenue to design the strain by single-atom for sustainable energy conversion technologies.

Exploring the Influence of Cation and Halide Substitution in the Structure and Optical Properties of CH3NH3NiCl3 Perovskite.

This manuscript details a comprehensive investigation into the synthesis, structural characterization, thermal stability, and optical properties of nickel-containing hybrid perovskites, namely CH3NH3NiCl3, CsNiCl3, and CH3NH3NiBrCl2. The focal point of this study is to unravel the intricate crystal structures, thermal behaviors, and optical characteristics of these materials, thereby elucidating their potential application in energy conversion and storage technologies. X-ray powder diffraction measurements confirm that CH3NH3NiCl3 adopts a crystal structure within the Cmcm space group, while CsNiCl3 is organized in the P63/mmc space group, as reported previously. Such structural diversity underscores the complex nature of these perovskites and their potential for tailored applications. Thermal analysis further reveals the stability of CH3NH3NiCl3 and CH3NH3NiBrCl2, which begin to decompose at 260 °C and 295 °C, respectively. The optical absorption properties of these perovskites studied by UV-VIS-NIR spectroscopy revealed the bands characteristic of Ni2+ ions in an octahedral environment. Notably, these absorption bands exhibit subtle shifts upon bromide substitution, suggesting that optical properties can be finely tuned through halide modification. Such tunability is paramount for the design and development of materials with specific optical requirements. By offering a detailed examination of these properties, the study lays the groundwork for future advancements in material science, particularly in the development of innovative materials for sustainable energy technologies.

Cross-dimensional multi-physics model and two-phase mass-transport enhancement for the hydrogen peroxide-based fuel cell

The direct liquid fuel cell utilizing hydrogen peroxide as an oxidant is considered to be the promising energy conversion technology, owing to its superior energy density and theoretical voltage. In the hydrogen peroxide-based fuel cells, the ever-changing two-phase mass transport and multi-component reaction processes resulting from the hydrogen peroxide self-decomposition exerts a pivotal influence on their performance. In this work, taken hydrogen peroxide self-decomposition into account, a cross-dimensional multi-physics model for the hydrogen peroxide-based fuel cell was proposed and developed to clarify the complex mechanisms of transports and reactions. In this ingeniously developed model, the multi-component reaction in the porous electrode is elucidated by a two-dimensional (2D) sub-model, the two-phase mass transport in the flow field is captured by a three-dimensional (3D) sub-model, and the one-dimensional (1D) correlation equation is served as a bridge between them. The uneven distribution of gas–liquid volume, velocity and current density and their relationships in fuel cell with serpentine flow field and dot matrix flow field were thus achieved. Furthermore, a novel gradient dot matrix flow field was developed to match the two-phase mass transport and multi-component reaction processes of hydrogen peroxide-based fuel cell. It is found that the continuously increasing pressure and velocity along flow path is balanced by the gradient-downsized ribs and the formation of large-volume oxygen bubbles is prevented by the gradient-densified ribs, achieving obviously uniformized current density distribution. Moreover, the gradient dot matrix flow field enables 54 % higher average hydrogen peroxide coverage contents (49 %) and 86 % lower average pressure drop (172 Pa) compared to the serpentine flow field, yielding 6.3 % higher peak power density (210 mW cm−2) and ultra-low extra pump power in fuel cell. This work will make contribution towards gaining profound insights into the intricate mechanisms underlying mass and charge transport, and offering invaluable guidance for the flow field design for the hydrogen peroxide-based fuel cells.

Flexible Ultrasonic‐Induced Wireless Energy Conversion Technology in Implantable Biomedicine

AbstractNumerous associated challenges arise with the advancement and continuous improvement of implantable medical devices, such as the frequent requirement for battery replacement. The flexible ultrasonic‐induced wireless energy conversion (UWEC) technology has garnered significant interest due to its superior energy transmission efficiency, safety, and biocompatibility compared to traditional electromagnetic wireless energy conversion technology. This paper provides a comprehensive review of the recent advancements in two types of flexible UWEC technologies, triboelectric nanogenerators, and piezoelectret nanogenerators, with a focus on their applications in implantable medical treatments. First, the energy conversion principles and general materials of flexible UWEC are presented. Then, the research and application of flexible UWEC devices are introduced in detail based on their medical functions. At the end of this review, perspectives and opportunities are discussed.

Nickel adsorbed algae biochar based oxygen reduction reaction catalyst

Lately, the bio electrochemical systems are emerging as an efficient wastewater treatment and energy conversion technology. However, their scaling-up is considerably restrained by slow-rate of cathodic oxygen reduction reaction (ORR) or otherwise by the high cost associated with the available efficient ORR catalysts. In this investigation, a cost-effective and eco-friendly approach for synthesizing Ni based ORR catalyst utilizing biosorption property of microalgae is accomplished. The synthesised Ni adsorbed algal biochar (NAB) served as an efficient cathode catalyst for enhancing ORR in a microbial carbon-capture cell (MCC). On increasing the initial concentration of Ni2+ in the aqueous medium from 100 mgL−1 to 500 mgL−1, the biosorption capacity was found to increase from 3 mgg−1 to 32 mgg−1 of algae cell. The MCC operated with NAB based cathode catalyst loading of 2 mgcm-2 exhibited 3.5 times higher power density (4.69 Wm−3) as compared to the one with commercial activated carbon. A significant organic matter removal (82 %) in the anodic chamber with simultaneous algal biomass productivity in the cathodic chamber was attained by MCC with cathode loaded with 2 mgcm−2 of NAB. Hence, this easily synthesised low-cost catalyst, out of waste stream, proved its ability to improve the performance of MCC.

AI-Driven Ensemble Learning for Accurate Seebeck Coefficient Prediction in Half-Heusler Compounds Based on Chemical Formulas.

Half-Heusler compounds with their unique crystal structure and tunable properties show excellent thermoelectric properties. As a result, these compounds hold great potential for many applications such as thermoelectric devices and energy conversion technologies. This paper presents a machine learning study on developing ensemble learning models to accurately predict the Seebeck coefficient at ambient temperature and arbitrary carrier concentration for both n-type and p-type half-Heusler compounds, based only on their chemical formula. Ensemble learning algorithms proved to be effective regression models for identifying hidden relationships. All models displayed satisfactory performance under 10-fold cross-validation and achieved high R-squared values ranging from 0.87 to 0.95 and low MAE values ranging from 20.8 μV/K to 37.04 μV/K. Among ensemble models, the GBoost shows the best performance for p-type with an R2 value of 0.95. On the other hand, for n-type the Light GBoost and CatBoost models yielded the best results with R2=0.94. Ultimately, we validated the accuracy of the model outputs through rigorous Density Functional Theory (DFT) calculations, wherein these models demonstrated their remarkable effectiveness in precisely predicting the Seebeck coefficients for half-Heusler compounds. This research holds significant potential in facilitating the screening of materials for thermoelectric devices, which heavily rely on the critical Seebeck coefficient parameter. The ability to accurately predict this key property can accelerate the identification of promising candidate materials, driving advancements in thermoelectric technology and paving the way for more efficient energy conversion and management solutions.

Investigation of Water Impacts on Surface Properties and Performance of Air-Electrode in Reversible Protonic Ceramic Cells.

Water, being abundant and readily accessible, gains widespread usage as proton source in many catalysis and energy conversion technologies, including applications like reversible protonic ceramic cells (R-PCCs). Revealing the influence of water on the electrode surface and reaction kinetics is critical for further improving their electrochemical performance. Herein, a hydrophilic air-electrode PrBa0.875Cs0.125Co2O5+δ is developed for R-PCC, which demonstrates a remarkable peak power density of 1058mWcm-2 in fuel cell mode and a current density of 1354mAcm-2 under 1.3V in electrolyzing steam at 650°C. For the first time on R-PCC, surface protons' behavior in response to external voltages is captured using in situ FTIR characterizations. Further, it is shown that contrary to the bulk proton uptake process that is thought to follow hydrogenation reactions and lead to cation reductions. The air-electrode presents enriched surface protons occurring through oxidizing surface cations, as confirmed by depth-profiling XPS results. H/D isotope exchange experiments and subsequent electrochemical characterization analyses reveal that the presence of protons enhances surface reactions. This study fills the knowledge gap between water-containing atmospheres and electrochemical performance by providing insights into the surface properties of the material. These new findings provide guidance for future electrode design and optimization.

Synergistic modulation of the d-band center in Ni3S2 by selenium and iron for enhanced oxygen evolution reaction (OER) and urea oxidation reaction (UOR)

Efficient production of green hydrogen energy is crucial in addressing the energy crisis and environmental concerns. The oxygen evolution reaction (OER) poses a challenge in conventional overall water electrolysis due to its slow thermodynamically process. Urea oxidation reaction (UOR) offers an alternative anodic oxidation method that is highly efficient and cost-effective, with favorable thermodynamics and sustainability. Recently, there has been limited research on bifunctional catalysts that exhibit excellent activity for both OER and UOR reactions. In this study, we developed a selenium and iron co-doped nickel sulfide (SeFe-Ni3S2) catalyst that demonstrated excellent Tafel slopes of 53.9 mV dec−1 and 16.4 mV dec−1 for OER and UOR, respectively. Density Functional Theory (DFT) calculations revealed that the introduction of metal (iron) and nonmetallic elements (selenium) was found to coordinate the d-band center, resulting in improved adsorption/desorption energies of the catalysts and reduced the overpotentials and limiting potentials for OER and UOR, respectively. This activity enhancement can be attributed to the altered electronic coordination structure after the introduction of selenium (Se) and iron (Fe), leading to an increase in the intrinsic activity of the catalyst. This work offers a new strategy for bifunctional catalysts for OER and UOR, presenting new possibilities for the future development of hydrogen production and novel energy conversion technologies It contributes towards the urgent search for technologies that efficiently produce green hydrogen energy, providing potential solutions to mitigate the energy crisis and protect the environment.

Electrochemistry of 2D-materials for the remediation of environmental pollutants and alternative energy storage/conversion materials and devices, a comprehensive review

This review article explores into the complicated relationship between electrochemistry and 2D materials, exploring their mutual influences and the consequential advancements in energy conversion, storage, and environmental applications. Electrochemical reactions, manifested through oxidations and reductions at submerged electrodes, form the linchpin connecting the electrochemistry of 2D materials with their practical utility. Various electrochemical cell topologies are investigated for their role in enhancing material flexibility, operational states, energy conversion efficiency, and device design adaptability. The comprehensive discussion extends to diverse applications, emphasizing the pivotal roles of 2D materials in environmental remediation, alternate energy storage and conversion, and chemical reactivity. Noteworthy applications include pollutant detection, adsorption and absorption of pollutants, elimination of both organic and inorganic pollutants, and photocatalytic degradation. The review also addresses materials synthesis via electrochemical processes, detailing functionalization, handling, and deposition techniques. Particular focus is directed towards local electrochemical techniques enabling the analysis and local alteration of 2D materials. Moreover, this paper concludes the article published in the recent years with this topic and most significant trends observed in 2022 and 2023 with electrochemistry of materials for the remediation of environmental pollutants. While the trends of article publishing increased from 2020 to 2023 with topic alternative energy storage/conversion materials. Finally, offering a comprehensive overview of the synergistic relationship between electrochemistry and 2D materials and their transformative potential in sustainable technologies. Broader contextThe decreasing availability of energy resources and the contamination of the environment are two significant worldwide concerns that need immediate attention. The focus on 2D materials and associated technologies is important for the efficient conversion of solar energy into chemical energy. These materials have diverse applications in fields such as energy (e.g., water splitting), synthesis (e.g., production of valuable chemicals and N2 reduction), and the environment (e.g., CO2 reduction and environmental remediation). Furthermore, Electrochemical energy storage and conversion (EESC) technologies are widely acknowledged as the most viable solutions to address the escalating energy crisis and environmental degradation because to their exceptional energy efficiency and little environmental footprint. Currently, there have been several reports discussing the use of 2D-materials in energy applications and wastewater treatment. However, there is a lack of comprehensive reviews that summarize the electrochemistry of 2D-materials, their preparation strategies, modification techniques, and related properties. Furthermore, there is a need for detailed analysis of the progress in applying 2D-materials for environmental pollution remediation, electrocatalytic performance, energy storage, and conversion technologies and devices. In this paper, we systematically and comprehensively review the electrochemistry of 2D-materials and innovatively analyze the design principles and difficulties of 2D-materials. We discussed comprehensively the remediation of environmental pollutants through 2D-materials in water treatment fields such as photocatylsts, adsorption/absorption and dyes removal as an entry point and provide an in-depth knowledge and outlook on the current status and development potential of specific applications of energy storage and conversion materials and devices.