Electrocatalytic Water Splitting Research Articles

Top-down nanostructured multilayer MoS2 with atomically sharp edges for electrochemical hydrogen evolution reaction

Cost-efficient and readily scalable platinum-free electrocatalysts are crucial for a smooth transition to future renewable energy systems. Top-down activation of MoS2 promises the production of sustainable hydrogen evolution electrocatalysts from the Earth-abundant molybdenite ore. Here, the deterministic nanopatterning of multilayer MoS2 with numerous zigzag edges is explored as a pathway to enhance hydrogen evolution reaction (HER). Nanopatterned single-nanosheet MoS2 electrodes are assessed by two highly localized electrochemical techniques: selected area voltammetry (with lithography-defined regions of electrode-electrolyte contact) and Scanning ElectroChemical Microscopy (SECM). The nanopatterning effect is the most pronounced after prolonged electrochemical cycling in an acidic electrolyte. The electrocatalytic hydrogen evolution activity of edge-enriched electrodes is dramatically enhanced: the maximum electrochemical current density (jmax) achieved at -510 mV vs. reversible hydrogen electrode (mVRHE) is increased by two orders of magnitude, reaching >300 mA⋅cm−2. Both the η10 and η100 overpotentials are significantly reduced as well. Meanwhile, pristine MoS2 shows just ≈6 times jmax increase (≈30 mA⋅cm−2) after the very same cycling. The increased electrocatalytic activity comes with electrode morphology degradation, evidenced by ex-situ scanning electron microscopy. SECM directly visualizes stronger HER activity in the regions with densely located zigzag edges. Intense white light illumination significantly boosts HER on MoS2 electrodes due to the photo-enhanced MoS2 conductivity. These results improve the understanding and reveal the limitations of MoS2-based electrocatalytic water splitting.

Carbon Nanotube Composites with Bimetallic Transition Metal Selenides as Efficient Electrocatalysts for Oxygen Evolution Reaction

Hydrogen fuel is a clean and versatile energy carrier that can be used for various applications, including transportation, power generation, and industrial processes. Electrocatalytic water splitting could be the most beneficial and facile approach for producing hydrogen. In this work, transition metal selenide composites with carbon nanotubes (CNTs) have been investigated for electrocatalytic water splitting. The synthesis process involved the facile one-step hydrothermal growth of transition metal nanoparticles over the CNTs and acted as an efficient electrode toward electrochemical water splitting. Scanning electron microscopy and XRD patterns reveal that nanoparticles were firmly anchored on the CNTs, resulting in the formation of composites. The electrochemical measurements reveal that CNT composite with nickel–cobalt selenides (NiCo-Se/CNTs@NF) display remarkable oxygen evolution reaction (OER) activity in basic media, which is an important part of hydrogen production. It demonstrates the lowest overpotential (η10mAcm−2) of 0.560 V vs. RHE, a reduced Tafel slope of 163 mV/dec, and lower charge transfer impedance for the OER process. The multi-metallic selenide composite with CNTs demonstrating unique nanostructure and synergistic effects offers a promising platform for enhancing electrocatalytic OER performance and opens up new avenues for efficient energy conversion and storage applications.

2D Monolayer Catalysts: Towards Efficient Water Splitting and Green Hydrogen Production.

A viable alternative to non-renewable hydrocarbon fuels is hydrogen gas, created using a safe, environmentally friendly process like water splitting. An important role in water-splitting applications is played by the development of two-dimensional (2D) layered transition metal chalcogenides (TMDCs), transition metal carbides (MXenes), graphene-derived 2D layered nanomaterials, phosphorene, and hexagonal boron nitride. Advanced synthesis methods and characterization instruments enabled an effective application for improved electrocatalytic water splitting and sustainable hydrogen production. Enhancing active sites, modifying the phase and electronic structure, adding conductive elements like transition metals, forming heterostructures, altering the defect state, etc., can improve the catalytic activity of 2D stacked hybrid monolayer nanomaterials. The majority of global research and development is focused on finding safer substitutes for petrochemical fuels, and this review summarizes recent advancements in the field of 2D monolayer nanomaterials in water splitting for industrial-scale green hydrogen production and fuel cell applications.

Subtle 2D/2D MXene-Based Heterostructures for High-Performance Electrocatalytic Water Splitting.

Developing efficient electrocatalysts is significant for the commercial application of electrocatalytic water splitting. 2D materials have presented great prospects in electrocatalysis for their high surface-to-volume ratio and tunable electronic properties. Particularly, MXene emerges as one of the most promising candidates for electrocatalysts, exhibiting unique advantages of hydrophilicity, outstanding conductivity, and exceptional stability. However, it suffers from lacking catalytic active sites, poor oxidation resistance, and easy stacking, leading to a significant suppression of the catalytic performance. Combining MXene with other 2D materials is an effective way to tackle the aforementioned drawbacks. In this review, the focus is on the accurate synthesis of 2D/2D MXene-based catalysts toward electrocatalytic water splitting. First, the mechanisms of electrocatalytic water splitting and the relative properties and preparation methods of MXenes are introduced to offer the basis for accurate synthesis of 2D/2D MXene-based catalysts. Then, the accurate synthesis methods for various categories of 2D/2D MXene-based catalysts, such as wet-chemical, phase-transformation, electrodeposition, etc., are systematically elaborated. Furthermore, in-depth investigations are conducted into the internal interactions and structure-performance relationship of 2D/2D MXene-based catalysts. Finally, the current challenges and future opportunities are proposed for the development of 2D/2D MXene-based catalysts, aiming to enlighten these promising nanomaterials for electrocatalytic water splitting.

Generic heterostructure interfaces bound to Co9S8 for efficient overall water splitting supported by photothermal

The increase of reaction temperature of electrocatalysts and the construction of heterogeneous structures is regarded as an efficient method to improve the electrocatalytic water splitting activity. Here, we report an approach to enhance the local heat and active sites of the catalyst by building a heterostructure with Co9S8 to significantly improve its electrocatalytic performance. The as-fabricated Co9S8@Ce-NiCo LDH/NF electrode possesses a notable photothermal ability, as it effectively converts near-infrared (NIR) light into the local heat, owing to its significant optical absorption. Leveraging these favorable qualities, the prepared Co9S8@Ce-NiCo LDH/NF electrode showed impressive performance in both hydrogen evolution reaction (HER) (η100 = 144 mV) and oxygen evolution reaction (OER) (η100 = 229 mV) under NIR light. Compared to the absence of the NIR light, the presence of NIR irradiation leads to a 24.6 % increase in catalytic efficiency for HER and a 15.8 % increase for OER. Additionally, other dual-functional electrocatalysts like NiCo-P, NiFeMo, and NiFe(OH)x also demonstrated significantly enhanced photothermal effects and improved catalytic performance owing to the augmented photothermal conversion when combined with Co9S8. This work offers novel pathways for the development of photothermal-electrocatalytic systems that facilitate economically efficient and energy-conserving overall water splitting processes.

APA-graphene: A multifunctional material for lithium-ion batteries and electrocatalytic water splitting

In Lithium-ion batteries (LIBs) and electrocatalytic water splitting, two promising technologies for future clean energy storage and regeneration, exploring electrode materials with excellent properties is critical for facilitating reaction kinetics and enhancing energy utilization efficiency. Starting from the successfully synthesized polyazulene carbon fragment, we designed a new two-dimensional (2D) carbon allotrope, anti-polyazulene graphene (APA-graphene). The robust stability of APA-graphene, along with the fact that nanoribbons of TPH-graphene and phagraphene have been successfully synthesized from 2,6-polyazulene chains, strongly indicate the high feasibility of experimental synthesis for APA-graphene. The metallic nature of APA-graphene, along with its distinctive anisotropic mechanical properties, which encompass the rare negative Poisson's ratios (−0.04 ∼ − 0.37 in all directions), has been predicted through first-principles calculations. It also shows high feasibility as an anode material for LIBs, with a large Li adsorption energy (−0.52 eV), low energy barrier for Li diffusion (0.25 eV), substantial maximum Li storage capacity (558 mAh/g), and low average open circuit voltage (0.16 V). Furthermore, APA-graphene demonstrates remarkable capability in the electrocatalytic dissociation of water molecules, with lower overpotentials for hydrogen and oxygen evolution reactions (0.04 and 0.83 V, respectively) compared to most known electrocatalysts. Overall, APA-graphene is a multifunctional material with exceptional performance, showcasing its great potential for applications in future clean energy technology.

Ni-Xides (B, S, and P) for Alkaline OER: Shedding Light on Reconstruction Processes and Interplay with Incidental Fe Impurities as Synergistic Activity Drivers.

Ni-Xides (X = B, P, or S) exhibit intriguing properties that have endeared them for electrocatalytic water splitting. However, the role of B, P, and S, among others, in tailoring the catalytic performance of the Ni-Xides remains vaguely understood, especially if they are studied in unpurified KOH (Un-KOH) because of the renowned impact of incidental Fe impurities. Therefore, decoupling the effect induced by Fe impurities from inherent material reconstruction processes necessitates investigation of the materials in purified KOH solutions (P-KOH). Herein, studies of the OER on Ni2B, Ni2P, and Ni3S2 in P-KOH and Un-KOH coupled with in situ Raman spectroscopy, ex situ post-electrocatalysis, and online dissolution studies by ICP-OES are used to unveil the distinctive role of Ni-Xide reconstruction and the role of Fe impurities and their interplay on the electrocatalytic behavior of the three Ni-Xide precatalysts during the OER. There was essentially no difference in the OER activity and the electrochemical Ni2+/Ni3+ redox activation fingerprints of the three precatalysts via cyclic voltammetry in P-KOH, whereas their OER activity was considerably higher in Un-KOH with marked differences in the intrinsic activity and evolution of the Ni2+/Ni3+ fingerprint redox peaks. Thus, in the absence of Fe in the electrolyte (P-KOH), neither the nature of the guest element (B, P, and S) nor the underlying reconstruction processes are decisive activity drivers. This underscores the crucial role played by incidental Fe impurities on the OER activity of Ni-Xide precatalysts, which until now has been overlooked. In situ Raman spectroscopy revealed that the nickel hydroxide derived from Ni2B exhibits higher disorder than in the case of Ni2P and Ni3S2, both exhibiting a similar degree of disorder. The guest elements thus influence the degree of disorder of the formed nickel oxyhydroxides, which through their synergistic interaction with incidental Fe impurities concertedly realize high OER performance.

Recent Progress of Ru Single‐Atom Catalyst: Synthesis, Modification, and Energetic Applications

AbstractIn recent years, single‐atom catalysts (SACs) have become the most active part of the catalytic field due to their excellent catalytic activity. Among them, Ru SACs exhibit excellent performance in many catalytic applications due to their high atomic utilization efficiency, catalytic activity and selectivity, and relatively low cost. In order to understand the structure–performance relationship and potential catalytic mechanism of Ru SACs, this review summarizes the research progress of Ru SACs in the fields of electrocatalytic water splitting, fuel cells, nitrogen reduction, and nitrate reduction in recent years. The catalytic process of Ru single atom in different synthesis methods and modification strategies is summarized. Finally, some opportunities and challenges for the future development of Ru SACs are prospected.

Ion-exchange strategy for fabricating highly dispersed Co–MoS2 on N-doped graphene for efficient bifunctional electrocatalytic water splitting

Recently, the pivotal to electrocatalytic water splitting is developing efficient and earth-abundant electrocatalysts to accelerate the sluggish kinetics of hydrogen and oxygen evolution reactions (HER and OER). In this work, (NH4)2MoS4 derived from polyoxometalates ((NH4)6Mo7O24·4H2O) were immobilized onto the ion exchange resin D314, and highly dispersed Co-molybdenum disulfide (Co–MoS2@NG-4) on nitrogen-doped graphene catalyst was prepared. The optimized Co–MoS2@NG-4 shows excellent electrocatalytic performance for HER and OER. Specifically, the low overpotentials of 202 and 352 mV are required to drive the current density of 10 mA cm−2 with the small Tafel slope of 77.30 and 153.50 mV dec−1 for HER and OER, respectively. The Co–MoS2@NG-4 demonstrates excellent stability, maintaining a robust operation for 5000 cyclic tests with no detectable stability decay.

Carbon-based electrocatalysts for water splitting at high-current-densities: A review

Electrocatalytic water splitting is a promising strategy to generate hydrogen using renewable energy under mild conditions. Carbon-based materials have attracted attention in electrocatalytic water splitting because of their distinctive features such as high specific area, high electron mobility and abundant natural resources. Hydrogen produced by industrial electrocatalytic water splitting in a large quantity requires electrocatalysis at a low overpotential at a large current density. Substantial efforts focused on fundamental research have been made, while much less attention has been paid to the high-current-density test. There are many distinct differences in electrocatalysis to split water using low and high current densities such as the bubble phenomenon, local environment around active sites, and stability. Recent research progress on carbon-based electrocatalysts for water splitting at low and high current densities is summarized, significant challenges and prospects for carbon-based electrocatalysts are discussed, and promising strategies are proposed.

Charge redistribution on NiCo-P hybrid nanoneedle via Br doping enables highly HER

Designing and manufacturing a catalyst with promoted activity and robust stability plays a great role in hydrogen production through electrocatalytic water splitting, but it still remains a great challenge. Herein, this paper reports a porous Br doping NiCoP nanoneedles grown onto the coarsen nickel foam (NF/Ni@Br-NiCoP NNs) through a sequential process of electrodeposition, hydrothermal, and thermal phosphorization. The characterization demonstrates that Br enhanced the electric conductivity and regulated the electron structure, thus leading to a proper H absorption energy (ΔGH*) of –0.13 eV. As a sequence, the NF/Ni@Br-NiCoP NNs only needs 35 (170 mV) to reach 10 (100 mA cm−2) for HER. In addition, the NF/Ni@Br-NiCoP NNs exhibits long-term durability for HER, which the overpotential increased by approximately 3.84 % post 100 h at 50 mA cm−2. Additionally, the KSCN poisoning experiment and first-principle density function theory (DFT) calculation reveal that the Co served as the active site due to the most proper ΔGH*. Moreover, the in-situ Raman spectroscopies characterization indicates that the Ni(OH)2 and α-Co(OH)2 were generated in HER. Hence, this study not only demonstrates a facile synthesis route to prepare HER catalysts, but also establishes a detailed understanding of the interaction between crystal structure, morphology, and electrocatalytic activity.

Metallic Nanoclusters for Electrochemical Water Splitting

AbstractElectrocatalytic water splitting is regarded as one of the most promising strategies for producing clean and sustainable energy sources (H2 and O2) in cathodic hydrogen evolution reaction (HER) and anodic oxygen evolution reaction (OER), respectively. Currently, transition metal nanoparticles (NPs) such as commercial Pt/C, IrO2, and RuO2 are still popular catalysts for industrial‐level HER and OER processes. However, both the high cost and low atomic utilization of NPs can not satisfy the requirements of atomic economy and green chemistry. Compared with NPs, metallic nanoclusters (NCs), which have higher atom utilization and optimized electronic structure than NPs, show unique activities for water splitting. In this review, the recently reported advanced design strategies for preparing various NCs are discussed in detail. The methods to control the particle size, coordinated environment, and morphology of NCs are also summarized. The electrochemical activity and stability of NCs can be influenced by the synergistic effect between NCs and supporting materials, which is also mentioned. Then, the recently reported state‐of‐art‐catalysts for both HER and OER along with the detailed catalytic mechanism are described to show the advanced design principles. Finally, the future perspectives and some remaining challenges are also presented.

Excellent Bifunctional Water Electrolysis Activities of α-MoO3/AC Nanocomposites

Electrocatalytic water splitting is a cost-effective and environment-friendly technique for producing oxygen and hydrogen through the oxygen/hydrogen evolution reaction (OER/HER). Developing the highly active and stable electrocatalyst, particularly for bifunctional water electrolysis (i.e., both OER and HER), is still a formidable challenge. Herein, we demonstrated the enhanced bifunctional water splitting activities by utilizing the molybdenum trioxide-anchored activated carbon (MoO3/AC) nanocomposites. The MoO3/AC samples were fabricated by the ultrasonication method using sol-gel synthesized MoO3 and biomass-derived AC, and they displayed a nanostreusel-like morphology with spherical MoO3 nanoparticle-decorated AC nanosheets. For the water electrolysis test, the MoO3/AC nanocomposites exhibited the excellent bifunctional electrocatalytic OER and HER performances with low overpotential and small Tafel slope values. Through analyzing the material characteristics and the electrochemical properties of MoO3/AC, it was found that the superb bifunctional OER-HER activities were attributed to the synergistic effects from the hybridization of highly conductive AC and electrochemically active α-MoO3. The results pronounce that the MoO3/AC nanocomposites possess an aptitude as a superb bifunctional OER/HER electrocatalyst for high-performance water electrolysis.

Spinel-type high-entropy oxide nanotubes for efficient oxygen evolution reaction

Oxygen evolution reaction (OER) involved 4-electron transfers is generally considered as the bottleneck for electrocatalytic water splitting. High-entropy oxides (HEO) show promising potential for OER due to their flexible structures and tunable compositions. Herein, we report a facile strategy to synthesize spinel-type (FeCoNiMnCr)3O4 HEO nanotubes (NTs) with unique hollow structures by combining electrospinning process and calcination treatment. The (FeCoNiMnCr)3O4 HEO NTs prepared at 400 °C exhibit the low overpotential of 353 mV at 50 mA cm−2 and small Tafel slope of 55.6 mV dec−1 in 1 M KOH electrolyte. The three-dimensional (3D) nanofiber-based architecture ensure the superior stability, as evidenced by the stable current density under continuous OER process for more than 60 h. Meanwhile, the hollow structure provides abundant exposed active sites, which could significantly improve the OER activity. This work provides new design of low-cost and high-efficient HEO with ensemble active sites for OER.

MOF-based/derived catalysts for electrochemical overall water splitting

Water-splitting electrocatalysis has gained increasing attention as a promising strategy for developing renewable energy in recent years, but its high overpotential caused by the unfavorable thermodynamics has limited its widespread implementation. Therefore, there is an urgent need to design catalytic materials with outstanding activity and stability that can overcome the high overpotential and thus improve the electrocatalytic efficiency. Metal-organic frameworks (MOFs) based and/or derived materials are widely used as water-splitting catalysts because of their easily controlled structures, abundant heterointerfaces and increased specific surface area. Herein, some recent research findings on MOFs-based/derived materials are summarized and presented. First, the mechanism and evaluation parameters of electrochemical water splitting are described. Subsequently, advanced modulation strategies for designing MOFs-based/derived catalysts and their catalytic performance toward water splitting are summarized. In particular, the correlation between chemical composition/structural functionalization and catalytic performance is highlighted. Finally, the future outlook and challenges for MOFs materials are also addressed.

Chaotropic Nanoelectrocatalysis: Chemically Disrupting Water Intermolecular Network at the Point‐of‐Catalysis to Boost Green Hydrogen Electrosynthesis

AbstractEfficient green hydrogen production through electrocatalytic water splitting serves as a powerful catalyst for realizing a carbon‐free hydrogen economy. However, current electrocatalytic designs face challenges such as poor hydrogen evolution reaction (HER) performance (Tafel slope, 100–140 mV dec−1) because water molecules are thermodynamically trapped within their extensive hydrogen bonding network. Herein, we drive efficient HER by manipulating the local water microenvironment near the electrocatalyst. This is achieved by functionalizing the nanoelectrocatalyst's surface with a monolayer of chaotropic molecules to chemically weaken water‐water interactions directly at the point‐of‐catalysis. Notably, our chaotropic design demonstrates a superior Tafel slope (77 mV dec−1) and the lowest overpotential (0.3 V at 10 mA cm−2ECSA), surpassing its kosmotropic counterparts (which reinforces the water molecular network) and previously reported electrocatalytic designs by up to ≈2‐fold and ≈3‐fold, respectively. Comprehensive mechanistic investigations highlight the critical role of chaotropic surface chemistry in disrupting the water intermolecular network, thereby releasing free/weakly bound water molecules that strongly interact with the electrocatalyst to boost HER. Our study provides a unique molecular approach that can be readily integrated with emerging electrocatalytic materials to rapidly advance the electrosynthesis of green hydrogen, holding immense promise for sustainable chemical and energy applications.

High-throughput electrochemical strategy for synthesis of iron-based nanostructures for electrocatalytic water splitting

High-throughput electrochemical strategy for synthesis of iron-based nanostructures for electrocatalytic water splitting

Chaotropic Nanoelectrocatalysis: Chemically Disrupting Water Intermolecular Network at the Point-of-Catalysis to Boost Green Hydrogen Electrosynthesis.

Efficient green hydrogen production through electrocatalytic water splitting serves as a powerful catalyst for realizing a carbon-free hydrogen economy. However, current electrocatalytic designs face challenges such as poor hydrogen evolution reaction (HER) performance (Tafel slope, 100-140 mV dec-1 ) because water molecules are thermodynamically trapped within their extensive hydrogen bonding network. Herein, we drive efficient HER by manipulating the local water microenvironment near the electrocatalyst. This is achieved by functionalizing the nanoelectrocatalyst's surface with a monolayer of chaotropic molecules to chemically weaken water-water interactions directly at the point-of-catalysis. Notably, our chaotropic design demonstrates a superior Tafel slope (77 mV dec-1 ) and the lowest overpotential (0.3 V at 10 mA cm-2 ECSA ), surpassing its kosmotropic counterparts (which reinforces the water molecular network) and previously reported electrocatalytic designs by up to ≈2-fold and ≈3-fold, respectively. Comprehensive mechanistic investigations highlight the critical role of chaotropic surface chemistry in disrupting the water intermolecular network, thereby releasing free/weakly bound water molecules that strongly interact with the electrocatalyst to boost HER. Our study provides a unique molecular approach that can be readily integrated with emerging electrocatalytic materials to rapidly advance the electrosynthesis of green hydrogen, holding immense promise for sustainable chemical and energy applications.

Surface Structure to Tailor the Electrochemical Behavior of Mixed-Valence Copper Sulfides during Water Electrolysis.

The semiconducting behavior of mixed-valence copper sulfides arises from the pronounced covalency of Cu-S bonds and the exchange coupling between CuI and CuII centers. Although electrocatalytic study with digenite Cu9S5 and covellite CuS has been performed earlier, detailed redox chemistry and its interpretation through lattice structure analysis have never been realized. Herein, nanostructured Cu9S5 and CuS are prepared and used as electrode materials to study their electrochemistry. Powder X-ray diffraction (PXRD) and microscopic studies have found the exposed surface of Cu9S5 to be d(0015) and d(002) for CuS. Tetrahedral (Td) CuII, distorted octahedral (Oh) CuII, and trigonal planar (Tp) CuI sites form the d(0015) surface of Cu9S5, while the (002) surface of CuS consists of only Td CuII. The distribution of CuI and CuII sites in the lattice, predicted by PXRD, can further be validated through core-level Cu 2p X-ray photoelectron spectroscopy (XPS). The difference in the electrochemical response of Cu9S5 and CuS arises predominantly from the different copper sites present in the exposed surfaces and their redox states. In situ Raman spectra recorded during cyclic voltammetric study indicates that Cu9S5 is more electrochemically labile compared to CuS and transforms rapidly to CuO/Cu2O. Contact-angle and BET analyses imply that a high-surface-energy and macroporous Cu9S5 surface favors the electrolyte diffusion, which leads to a pronounced redox response. Post-chronoamperometric (CA) characterizations identify the potential-dependent structural transformation of Cu9S5 and CuS to CuO/Cu2O/Cu(OH)2 electroactive species. The performance of the in situ formed copper-oxides towards electrocatalytic water-splitting is superior compared to the pristine copper sulfides. In this study, the redox chemistry of the Cu9S5/CuS has been correlated to the atomic arrangements and coordination geometry of the surface exposed sites. The structure-activity correlation provides in-depth knowledge of how to interpret the electrochemistry of metal sulfides and their in situ potential-driven surface/bulk transformation pathway to evolve the active phase.

N-type semiconductor [Gd3+-Ho3+-Dy3+]:SnO2 driven functionality enhancement in energy systems associated with photovoltaic and electrochemical contraptions

Current work reports the sustainable synthesis and application of the novel n-type [Gd3+-Ho3+-Dy3+]:SnO2 semiconductor material expressing band gap energy narrowing upon lanthanide triple doping. The band gap energy of this material spanned around 3.8–3.9 eV. Rare earth doped SnO2 material has tetragonal rutile crystalline geometry, space group P42/mnm, and 59.46 nm particle size. Thin films for this material have remarkable coverage. Using this material as an electron transport layer inside all inorganic perovskite device resulted in a negligible hysteresis leading to remarkable power conversion efficiency of 14.16 %, fill factor 80 %, short circuit current 16.48 mA cm−2, and an open circuit voltage of 1.02 V [Gd3+-Ho3+-Dy3+]:SnO2 decorated nickel foam electrode expressed double layer mechanism of electrical charge storage gaining a specific capacitance of 689 F g−1 in 0.1 M NaCl electrolyte at 10 mV/s. Excellent electronic and ionic conductivity was expressed by impedance studies with equivalent series resistance (Rs) of as low as 0.11 Ω. Furthermore, the electro-catalytic water splitting results exhibited the auspicious of this material as an HER catalyst with lower overpotential and Tafel slope values of 140 mV and 125.5 mV dec−1, respectively. The developed material is a suitable candidate for advanced energy applications marked by sustainability and economic viability.