Electrochemical Water Splitting Research Articles

Enhancement of BaCeO3 OER performance by generating a nanohybrid with gCN for electrochemical water splitting

Significant research is currently performed on electrochemical water splitting to solve ecological problems and energy issues. Sustainable and eco-friendly energy systems prefer to generate cost-effective electrocatalyst material with higher stability and excellent electrocatalytic activity to speed up the oxygen evolution reaction (OER) process. The current study followed a hydrothermal approach to develop a barium cerium oxide nanohybrid with g-CN (BaCeO3/g-CN) as an electro-catalyst for an efficient OER process in 1.0 M KOH. Physical characteristics analyses confirmed the enhanced activity of the synthesized BaCeO3 (BCO) and BCO/g-CN nanohybrid materials. The evaluated increased performance may be ascribed to improved morphological characteristics and substantial surface area (212 m2 g−1). The nanocomposite as mentioned above (BCO/g-CN) exhibits significant potential for effective OER in electrochemical assessments due to its abundant active spots and accelerated charge transfer process. Further, the electro-catalytic activity of the composite is improved, as demonstrated by a reduced overpotential (η = 210 mV) with Tafel value (36 mV dec−1) in comparison to pristine BCO (η = 262 mV and 52 mV dec−1) for OER. The material exhibited a reduced charge transfer impedance (Rct = 0.7 Ω), confirmed by EIS analysis. It also demonstrated a substantial ECSA (electrochemical active surface area) of 237.5 cm2 as compared to the pure BCO (137.5 cm2) material. Moreover, electrocatalyst material durability for 30 h was assessed by a chronoamperometric study. Thus, BCO/g-CN exhibits a notable rise in electrochemical properties, suggesting that it is a viable candidate for prospective OER applications.

Structural Regulation of NiFe LDH under Spontaneous Corrosion to Enhance the Oxygen Evolution Properties.

Electrochemical water splitting holds promise for sustainable hydrogen production but restricted by the sluggish reaction kinetics at the anodic oxygen evolution. Herein, we present a room-temperature spontaneous corrosion strategy to convert inexpensive iron (Fe) on iron foam substrates into highly active and stable self-supporting nickel iron layered hydroxide (NiFe LDH) catalysts. The corrosion evolution mechanisms are elucidated combining ex-situ scanning electron microscopy (SEM) and X-ray photo electron spectroscopy (XPS) techniques, demonstrating precise control over the concentration of Ni2+ and reaction time to achieve controllable micro-structures of NiFe LDH. Taking advantage of the self-supporting morphology and hierarchical micro-/nano- structure, the NiFe LDH with optimized Ni2+ concentration and reaction time exhibits significant small overpotentials of 160 mV and 200 mV for the OER at current densities of 10 mA cm-2 and 100 mA cm-2 respectively, showcasing excellent OER activities. Furthermore, this catalyst demonstrates superior reaction kinetics, high electrochemical stability, and excellent integral water splitting performance when coupled with a commercial Pt/C cathode. The energy-efficient, cost-effective, and scalable spontaneous corrosion strategy opens new avenues for the development of high-electrochemical-interface catalysts.

Multi-Component and Nanoporous Design toward RuO2-Based Electrocatalyst with Enhanced Performance for Acidic Water Splitting.

Developing electrocatalysts with excellent activity and stability for water splitting in acidic media remains a formidable challenge due to the sluggish kinetics and severe dissolution. As a solution, a multi-component doped RuO2 prepared through a process of dealloying-annealing is presented. The resulting multi-doped RuO2 possesses a nanoporous structure, ensuring a high utilization efficiency of Ru. Furthermore, the dopants can regulate the electronic structure, causing electron aggregation around unsaturated Ru sites, which mitigates Ru dissolution and significantly enhances the catalytic stability/activity. The representative catalyst (FeCoNiCrTi-RuO2) shows an overpotential of 167 mV at 10 mAcm-2 for oxygen evolution reaction (OER) in 0.5 m H2SO4 solution with a Tafel slope of 53.1mVdec-1, which is among the highest performance reported. Moreover, it remains stable for over 200 h at a current density of 10mAcm-2. This work presents a promising approach for improving RuO2-based electrocatalysts, offering a crucial advancement for electrochemical water splitting.

Oxygen evolution reaction activity of carbon aerogel supported Pd–Ni–Al catalysts synthesized by microwave irradiation method

The oxygen evolution reaction (OER) is a critical step for oxygen production during the electrochemical splitting of water. Effective OER catalysts support the development of clean energy technologies by increasing the energy efficiency of these processes. In this study, carbon aerogel (CA) was first synthesized as a catalyst support material using sol-gel, supercritical drying, and pyrolysis process. Then, mono-metallic (Pd/CA, Al/CA), bi-metallic (Pd–Al/CA, Pd–Ni/CA), and tri-metallic (Pd–Ni–Al/CA) catalysts were synthesized by microwave irradiation method. Inductively coupled plasma-mass spectrometry (ICP-MS), X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), Raman spectroscopy have been made to examine the structural properties of the synthesized catalysts. Electrochemical analysis was carried out through cyclic voltammetry (CV), chronoamperometry, and electrochemical impedance spectroscopy (EIS) in alkaline media (1 M KOH: Methanol) to examine the effect of metal loading of CA support material towards OER performance. All the compositions showed excellent activity toward OER, among all Pd–Ni/CA catalysts showed the highest activity. The OER peak current increased remarkably up to 48 mA cm−2 with methanol addition, which signifies the substantial application of carbon aerogel supported-Pd-Ni-Al catalysts in direct methanol fuel cells (DMFCs). Pd–Ni/CA display high OER performance with maximum diffusion coefficient, Do (6.6 × 10−8 cm2 s−1) and heterogeneous rate constant, ko (4.706 × 10−4 cm s−1), and smaller value of Tafel slope (128 mV dec−1). Electrochemical studies predicted that all the prepared carbon aerogel supported-Pd-Ni-Al catalysts can be used as efficient catalysts for OER and other related electrocatalysis applications.

Scalable synthesis of Co2C-covered NiTe (Co2C-NiTe) nanosheets as an efficient electrocatalyst for HER & OER in an alkaline medium

To tackle global carbon conditions, renewable energy-powered electrochemical water splitting is a promising energy conversion device that can enhance the sustainable hydrogen output of the next generation. Regarding large-scale water splitting, novel non-noble metal-based heterostructures focus on constructing highly efficient electrocatalysts with unique interfaces toward hydrogen and oxygen evolution reactions. In this work, to facilitate the limited number of defects in the pure Co2C and NiTe electrocatalysts, we report that NiTe nanoflakes are coupled with a dispersed nanosheet network of the Co2C to develop a Co2C-NiTe composite by interface engineering strategy using a hydrothermal approach. XRD, IV, BET, TEM, XPS, and EDX mapping technologies investigated the 3D structure of as-grown Co2C-NiTe/SS. Electrochemical test results revealed that our best-performing electrocatalyst delivers a 10 mAcm−2 with low overpotentials of 279 mV and 227 mV for oxidation and reduction reactions, respectively. Remarkably, this catalyst achieves good stability, reaching up to 90 h in one mol alkaline medium. We showed that this excellent activity of Co2C-NiTe is primarily due to the abundant interfacial area and stable anchoring sites, which improve the adsorption–desorption energy for hydroxide/oxyhydroxide species and thereby provide a fast electron transfer rate for OER/HER. In addition, a synergistic effect of Co2C with NiTe presents high electrical conductivity over counterpart electrocatalysts.

Zeolitic Imidazolate Framework-8 enhanced with tungsten carbide for high-performance hybrid supercapacitors and hydrogen evolution

A promising metal-organic framework (MOF) called Zeolitic Imidazolate Framework-8 (ZIF-8) stands out for its electrochemical applications. Its versatility in physicochemical properties makes it a strong candidate for breakthroughs in energy storage and electrochemical water splitting. The electrode nanomaterials lower specific capacity, small charging/discharging rate, and low conductivity limit its supercapacitor and hydrogen evaluation reaction (HER) applications. The ZIF-8 zeolite structure was decorated with tungsten carbide (WC) to overcome these issues. These modifications result in improved porosity, surface area, density, and pore size, shape, and structure. These characteristics contribute significantly to enhanced electrochemical activity. ZIF-8 MOF/WC nanocomposites have excellent dispersion and stability due to their porosity and strong connection between embedded WC nanoclusters and the framework. The prepared electrode showed a 118.11 mV overpotential and 36.45 mV/dec Tafel slope throughout HER activity. ZIF-8 MOF/WC was used for electrochemical studies and to make a hybrid energy storage device using activated carbon (AC). The hybrid supercapacitor had higher energy and power densities (87 W h/kg and 850 W/kg). The theoretical technique (Dunn model) was also employed to analyze experimental results more thoroughly.

Enriched edge sites of ultrathin Ni3S2/NiO nanomeshes promote surface reconstruction for robust electrochemical water splitting

Developing highly efficient nonnoble bifunctional electrocatalysts for both the H2 evolution reaction (HER) and O2 evolution reaction (OER) is essential but challenging for overall water splitting (OWS). Ni based catalysts are proved as promising candidates for water splitting, which usually undergo surface reconstruction by transforming into nickel oxyhydroxides as active sites. Although evidence suggests that the reconstruction originates from the exchange of surface lattice oxygen with the OH- in the electrolyte under electric field, modulating the reconstruction of Ni based catalysts remains a great challenge. Herein, we propose an edge sites enrichment strategy to promote the active phase evolution. The one-step synthesized ultrathin Ni3S2/NiO nanomeshes exhibited an ultrathin porous structure which contain abundant edge sites and Ni3S2/NiO in-plane interface sites. Owing to the unique structure, Ni3S2/NiO nanomeshes possessed an affinity feature to proton and OH-, resulting in a faster reconstruction from Ni3S2 to Ni(OH)2 than Ni3S2 bulk which subsequently converted into γ-NiOOH and a lower adsorption barrier for H*. Consequently, the Ni3S2/NiO nanomeshes exhibited outstanding OER activity (300 mV at 200 mA cm−2) and unexpected HER activity (73 mV at 10 mA cm−2) in 1.0 M KOH. Remarkably, the nanomeshes achieved an ultralow voltage of 1.41 V at 10 mA cm−2 with excellent stability for overall water splitting, which prevailed over most of the reported catalysts. Moreover, the nanomeshes performed a H2 yield of 900 µmol/h in a solar-assisted water splitting system with a H2 minimum sales price of $1.77/kg, much lower than that of the commercial catalyst ($7.18/kg). This work sets a new benchmark of monometallic bifunctional catalysts for industrial water splitting and provides new insights into the synthesis of 2D nanomeshes.

Rational Construction of a 3D Self-Supported Electrode Based on ZIF-67 and Amorphous NiCoP for an Enhanced Oxygen Evolution Reaction.

The development of efficient and Earth-abundant electrocatalysts for the oxygen evolution reaction (OER) is an urgent requirement in the field of electrochemical water splitting. The electrocatalytic performance of the OER can be greatly enhanced by the synergistic combination of zeolite imidazolate frameworks (ZIFs) and transition-metal phosphides, both of which individually exhibit promising capabilities in this regard. In this study, a novel amorphous NiCoP deposited on ZIF-67 sheets supported on Ni foam (labeled as NiCoP/ZIF-67/NF) as an OER electrocatalytic material was successfully synthesized using a simple, secure, and time-efficient two-step strategy. The experimental results demonstrate that NiCoP/ZIF-67/NF possesses a large active surface area with abundant active sites. Also, the synergistic effect and interaction between NiCoP and ZIF-67, as well as between Ni and Co within NiCoP, effectively enhance its electrochemical performance under alkaline conditions. Consequently, NiCoP/ZIF-67/NF exhibits outstanding catalytic activity for OER with an overpotential (η) of 175 mV at a current density of 10 mA cm-2 and a long-term stability over 40 h at 20 mA cm-2 in a 1.0 M KOH electrolyte. The corresponding analyses suggest that the real active sites responsible for the OER are identified as NiOOH and CoOOH species within the structure of NiCoP/ZIF-67/NF. Additionally, the catalytic function and stability of ZIF-67 toward the OER under alkaline conditions were also briefly discussed. This work provides a novel catalytic material for the OER along with a facile strategy to fabricate superior, efficient, and noble metal-free catalysts suitable for energy-related applications.

Three-dimensional pine-tree-like bimetallic sulfide with maximally exposed active sites by secondary structural restructuring for efficient electrocatalytic OER

Developing efficient, low-cost and bifunctional catalysts with predominant durability for the hydrogen evolution reaction (HER) and the oxygen evolution reaction (OER) is an extraordinary challenge in the preparation of green hydrogen energy by electrochemical water splitting. Three-dimensional (3D) transition metal compounds have become a research hotspot as OER electrocatalysts, which can replace noble metal oxides such as RuO2 and IrO2 to reduce application costs. Herein, we synthesized a novel three-dimensional pine-tree-like bimetallic sulfide arrays on nickel foam (FeCoS/NF) using various optimization strategies such as morphology optimization, in situ growth and introduction of heterogeneous structures. The as-synthesized FeCoS/NF electrocatalyst only requires relatively low overpotential of 156 mV to achieve a current density of 20 mA cm−2 for OER, with a Tafel slope of only 37 mV dec−1. It also has a small charge transfer resistance, an electrochemical surface area and good electrochemical stability in alkaline electrolytes. The excellent performance of FeCoS/NF can be attributed to the synergistic effect and amorphous phase of FeCoS as well as the well-defined pine-tree-like array architecture with a large surface area, abundant active sites, and sufficient gas and electrolyte diffusion channels.

Enhanced activity of electrodeposited WO3 thin films as bi-functional electrocatalysts for water splitting

The ultimate goal of the hydrogen economy is to develop an efficient and cost-effective electrocatalyst that can accelerate hydrogen synthesis from water without or with little additional energy. This study describes a unique surface modified electrodeposited nano-sized tungsten oxide (WO3) as an intriguing bi-functional electrocatalyst for OER in alkaline and HER in acidic conditions. The nano-WO3 was synthesized hydrothermally and electrodeposited on a fluorinated tin oxide (FTO) electrode. The highly uniform distribution of the WO3@FTO catalyst results in negligible charge transfer resistance, a large electroactive surface area, and increased water-splitting potential. During oxygen evolution reaction (OER), electrodeposited WO3@FTO initiates water splitting at an overpotential (η) of just 240 mV and represents a turnover frequency (TOF) of 0.59 sec−1. These results are comparable to previously reported electrocatalysts. Under an alkaline electrolyte, a current density of 15 mA/cm2 remained constant for several hours, indicating the high stability and durability of the electrodeposited WO3@FTO electrode. The electrode also performed well in hydrogen evolution reactions (HER). A Tafel slope of 46 mV/dec and −28 mV/dec was found for OER and HER, respectively, indicating an enhanced kinetics rate of reaction taking place at the electrode surface. Furthermore, in acidic conditions, the electrode represents a lower HER overpotential of 104 mV. The work provides a significant understanding of electrodeposited WO3@FTO electrodes and their role in electrochemical water splitting.

Two-Dimensional NiCo2S4 Nanosheets Deliver Efficient Oxygen Evolution Reaction

Introduction: The development of cost-effective and efficient catalysts plays a pivotal role in the realization of hydrogen production through electrochemical water splitting. Method: In this study, two-dimensional NiCo2S4 nanosheets weresynthesized usinga hydrothermal method followed by a sulfidation process. Results: The resulting materials were thoroughly characterized to understand their morphology and structure. The findings indicate that the NiCo2S4 nanosheets exhibit exceptional electrical conductivity and a high density of pores, which facilitate electrolyte infiltration and interfacial charge transfer during electrochemical reactions. Furthermore, the incorporation of S2− modulates the electronic structure of metal ions, reducing the oxidation potential of metal sites and promoting the surface reconstruction of the electrode to form active species. Electrochemical tests conducted in a 1 M KOH solution using the synthesized catalyst as the working electrode demonstrate an overpotential of merely 280 mV and 300 mV at a current density of 20 mA cm−2 and 40 mA cm−2 , respectively, which are much lower than those of NiCo-LDH electrodes (360 mV and 410 mV). Conclusion: Furthermore, the NiCo2S4 electrode delivers a remarkably low Tafel slope of 47.9 mV dec−1 . This investigation presents a novel approach to the development of efficient transition metal-based electrocatalysts.

BaTaO2N and quantum dots-based CuO nanocomposites for HER by solar electrochemical water splitting

Barium tantalum oxynitride (BaTaO2N) has been demonstrated to be an attractive catalyst for photo-electrochemical water splitting, especially oxygen evolution reactions. However, the hydrogen production rates and charge transfer resistances of BTN leave much to be desired from a practical standpoint. In fact, it has never been reported for photocathode applications. On the other hand, CuO has been reported for hydrogen evolution reactions. Given this, here nanocomposites of BaTaO2N and copper oxide quantum dots (CuO QDs), where the latter are digestively ripened, are reported for photoelectrochemical water splitting on a carbon paper substrate. To assess the role of ultra-small quantum dots, composites of commercially available CuO nanoparticles with BaTaO2N were also tested. BaTaO2N and CuO QD nanocomposites performed well and showed a high photocurrent density of 3.1 mA cm−2 at 0 V vs RHE. This was also accompanied by reduced charge transfer resistance (225.4 Ω) due to the high interfacial surface area provided by nanoscopic CuO on BaTaO2N.

Electrodeposition in one step: Synthesizing Ir–Co tetradecahedral nanoparticles with high-index (311) crystal planes for enhanced catalytic activity in alkaline hydrogen evolution reaction

Electrochemical water splitting represents a viable route for hydrogen production, but its efficiency critically depends on developing effective electrocatalysts that minimize energy loss and material costs. This study introduces iridium-cobalt (Ir–Co) nanoparticles were synthesized on copper foam (CF) substrates using a one-step electrodeposition method. A comprehensive analysis was conducted on the morphology, chemical composition, and crystal structure of the electrocatalysts, along with a particular study on their electrocatalytic performance in the hydrogen evolution reaction (HER). The results demonstrate that high-index IrCo (311) crystal planes have been detected in the Ir–Co/CF electrocatalysts, which possess a tetradecahedral polycrystalline structure. The size of tetradecahedral nanoparticles is in the range of 180–250 nm. Ir–Co nanoparticles exhibit a balanced composition of approximately 49.8 at% Ir and 50.2 at% Co. The Ir–Co/CF electrocatalyst exhibits superior electrocatalytic activity in 1.0 M KOH solution, requiring only 46.8 mV overpotential to obtain a current density of 10 mA cm−2, with a low Tafel slope of 32.65 mV·dec−1. Additionally, the prolonged stability tests confirm the robustness of the Ir–Co/CF electrocatalyst, highlighting its potential for sustainable energy applications.

Insight into the electrolyte concentration impact on single hydrogen bubble evolution dynamics at a microelectrode during electrochemical water splitting

Bubbles generated during electrochemical water splitting could adhere to the electrode surface and therefore impede the reaction. Thus, understanding and manipulating the evolution dynamics of bubbles is crucial for enhancing electrolysis efficiency. In this study, we investigated the evolution mechanism and forces acting on individual hydrogen bubble on Pt microelectrode surface by employing different H2SO4 electrolyte concentrations (0.2–1.0 M) under various applied voltages [−2 to −6 V vs saturated calomel electrode (SCE)]. We focused on bubble detachment diameter, average current, and bubble lifetime and subsequently established relational equations over these variables. At −6 V vs SCE, the growth coefficient has a maximum value of 14.42 × 10−4 m/s0.333 when the concentration of electrolyte is around 0.6 M. Gas production at 0.6 M increased by 63.4% compared to 0.2 M and by 11.2% compared to 1.0 M. Therefore, choosing the appropriate electrolyte concentration can maximize gas production and bubble detachment efficiency. Additionally, a force balance model incorporating the Marangoni force for single bubbles on the microelectrode surface was established across varying concentrations of H2SO4 electrolyte. At −4 V vs SCE, the solutal Marangoni force starts to dominate when electrolyte concentrations above 0.4 M. The results demonstrate the critical role of the solutal Marangoni force beyond a certain value of electrolyte concentration.

Silicon-doped cobal–aluminum layered double hydroxide electrocatalyst with high catalytic activity for oxygen evolution reactions

Electrochemical water splitting is a zero-carbon-emission and environmentally friendly method for hydrogen production. However, the process requires electrocatalysts to lower its energy requirements. In this study, Si-doped cobalt–aluminum layered double hydroxide (Si-CoAl-LDH) had been successfully synthesized by SiCl4 chemical etching at room temperature. The Co-O-Si chemical bonds promoted the formation of γ-CoOOHx during the process of water oxidation, thereby increasing the number of active sites. Moreover, Theoretical calculations revealed the overlap of atomic orbitals on the Si-CoAl-LDH catalyst surface and the improved electronic structure due to Co–O–Si chemical bonds. The Si-CoAl-LDH exhibited overpotentials of 295, 336, and 363 mV for oxygen evolution reactions (OERs) at current densities 10, 50, and 100 mA cm−2, respectively. The Tafel slope of the sample was 74.16 mV·dec−1. Physical characterization and in situ Raman analysis revealed the formation of intermediate hydroxylated cobalt species, which act as active centers during OER. This study serves as a basis for the surface reconstruction and activity enhancement of other electrocatalysts through Si doping.

Ion- and surface-sensitive interactions during oxygen evolution reaction in alkaline media

Abstract Clean and sustainable energy has turned towards electrochemical water splitting as a viable solution in minimizing carbon emissions. Electrolysis of water converts electrical energy to chemical energy, through the production of hydrogen and oxygen gases, which can be harnessed for potential applications without contributing to greenhouse emissions. While this energy storage process shows great potential, its efficiency is hindered by the sluggish kinetics of the oxygen evolution reaction (OER). As a result, its widespread application in green electrolytic technologies is limited hence investigations on improving OER kinetics are of utmost importance. Recent research breakthroughs indicate that alkali metal cations are more than passive observers. They play complex roles in the electric double layer (EDL), which positively influences the OER kinetics. The presence of numerous ions and their combinations presents a challenge of complexity. This study aims to delve into the impact of alkali metal cations on OER activity due to the variance in their hydration energies. Specific investigations focusing on different alkali metal cations in solution, such as Li+, Na+, and K+, was conducted on RuO2 to gain a deeper understanding of how these ions interact with both reactants and intermediate species in the reaction kinetics. Traditional electrochemical tests, including cyclic voltammetry (CV), linear sweep voltammetry (LSV), electrochemical impedance spectroscopy (EIS), and accelerated degradation test (ADT) measurements were employed to elucidate critical aspects such as surface activation, electric double layer interactions, catalytic activity and stability, ohmic resistance, and mass and charge transport.

Amorphous W-doped iron phosphide with superhydrophilic surface to boost water-splitting under large current density

Electrochemical water-splitting is an effective approach for producing hydrogen without producing any pollutants, but its large-scale development is hampered by the lack of low-cost and efficient electrocatalysts. Therefore, it is essential to explore efficient and low-cost non-precious catalysts for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). Herein, W-doped Fe-P/IF amorphous nanoflake arrays (W-Fe-P/IF) are synthesized by corrosive avenue and following low-temperature phosphorization. Benefiting from the superhydrophilic surface, amorphous structure, nanosheet morphology and abundant active sites, the synthesized catalysts exhibited good catalytic performance. Therefore, the W-Fe-P/IF electrocatalyst onws low overpotentials of 35, 67, and 105 mV to achieve 10 mA cm−2 in 1 M KOH, 1 M KOH + seawater, and 1 M PBS, respectively. In addition, it also exhibits low voltage of 1.63 V to obtain 10 mA cm−2 coupled with excellent stability under 500 mA cm−2. The work provides a new strategy for the preparation of highly-efficient and low-cost non-precious electrocatalysts on renewable energy-related applications.

CoFe hydroxide towards CoP2-FeP4 heterojunction for efficient and long-term stable water oxidation

Electrochemical water splitting stands out as a promising avenue for green hydrogen production, yet its efficiency is fundamentally governed by the oxygen evolution reaction (OER). In this work, we investigated the growth mechanism of CoFe hydroxide formed by in situ self-corrosion of iron foam for the first time and the significant influence of dissolved oxygen in the immersion solution on this process. Based on this, the CoP2-FeP4/IF heterostructure catalytic electrode demonstrates exceptional OER activity in a 1 M KOH electrolyte, with an overpotential of only 253 ± 4 mV (@10 mA cm−2), along with durability exceeding 1000 h. Density functional theory calculations indicate that constructing heterojunction interfaces promotes the redistribution of interface electrons, optimizing the free energy of adsorbed intermediate during the water oxidation process. This research highlights the importance of integrating self-corroding in-situ growth with interface engineering techniques to develop efficient water splitting materials.

Amorphous Cobalt-Impregnated Nitrogen-Doped Carbon Encapsulation Nanochain Enhances Long-Lasting Electrochemical Water Splitting.

Electrochemical water splitting (EWS) is a promising way to attain H2, which has been deemed an ideal substitution for fossil fuels because of renewable and eco-friendly benefits. Developing an amorphous-based simple and structurally flexible non-noble catalyst to offer high performance for commercial applications has become a current interest. Amorphous cobalt-anchored nitrogen-doped carbon nanoparticles (Co@NC-NPs) were designed to have a low overpotential and Tafel as a bifunctional electrocatalyst (HER - 142 mV/80 mV dec-1 and OER - 250 mV/72 mV dec-1) to achieve 10 mA cm-2 in 1.0 KOH. FE-SEM and HR-TEM described the interconnected nanochain morphology and purity of Co@NC-NPs electrocatalyst, which were confirmed by EDX and elemental mapping. In a full cell water electrolyzer, Co@NC-NPs(+,-) may act as an anode and cathode electrode material to achieve 1.60 V @ 10 mA cm-2 in a wide pH. The efficient Co@NC-NPs are stable for 100 h without obvious recession. In solar cell applications, Co@NC-NPs(+,-) catalyst was employed as both positive and negative terminals and evolved enormous bubbles of O2 and H2. As previously mentioned, we covered the amorphization strategy with the optimistic role of structural flexibility and defects to enrich the active sites to improve the electrocatalytic stability. As a promising opinion, the amorphous electrocatalyst provides ultraefficiency for forthcoming developments in EWS.

Solvent‐Less Synthesis of Compositionally Tuned Mixed Metal (Ni−Zn) Ferrites for Enhanced Electrocatalytic Water Splitting and Supercapacitance

AbstractExploring efficient, abundant, economical and stable materials for sustainable energy applications, such as electrochemical water splitting and supercapacitance, is a challenging task. Mixed transition metal spinel ferrites can rationally be customized to attain these features and deliver enhanced electrochemical activity. The catalytic performance of spinels is remarkably influenced by tuning the cationic occupancy at the tetrahedral or octahedral position. Herein, a set of spinel Ni1‐xZnxFe2O4 (0≤x≤1) nanocomposites were obtained via a scalable solventless thermolysis of metal acetylacetonate precursors at relatively mild temperatures. A suite of techniques such as powder p‐XRD, EDX, SEM, TEM, HRTEM, and SAED were employed to confirm the formation of the Ni−Zn ferrite solid solutions. It was found that small amounts of Ni at tetrahedral sites were beneficial for charge storage and hydrogen evolution. For instance, Ni0.2Zn0.8Fe2O4 nanocomposite demonstrated superior HER activity with a much lower overpotential of 87 mV compared to the pristine NiFe2O4 (213 mV) or ZnFe2O4 (164 mV) catalysts. However, Ni‐occupied tetrahedral sites were not suitable for OER, whereby the pristine ZnFe2O4 displayed high catalytic activity with an overpotential of 330 mV, outperforming other electrode compositions. The study helps to identify suitable compositions and site tuning for HER, OER and supercapacitors.