Nanosheet Arrays Research Articles

Hierarchical high K content birnessite MnO2 nanosheet arrays as high capacity cathode for asymmetric supercapacitor with broaden potential window of 2.6 V

High specific capacitance and energy density for energy storage devices are dependent on the types of electrodes selection and operational working potential windows. Birnessite MnO2 is reported as the astounding material to show strong electrochemical performances due to it's widen inter-planar spacing, capable to accommodate the alkaline ions for the better outcomes. Herein this article, high K content Birnessite MnO2 nanosheet arrays at carbon cloth substrate (K0.46MnO2 NSAs@CC) are successfully fabricated to optimize its structural, morphological and electrochemical performances as cathode for supercapacitors (SCs). K0.46MnO2 NSAs@CC is operated at broaden potential window from 0 to 1.3 V to achieve excellent specific capacitance of ∼375 F g−1. Reported broaden potential window provides the opportunity for the construction of aqueous asymmetric supercapacitors (ASC) to operate above 2.0 V. For the construction of efficient ASC, Bi2S3 nanoflakes interconnected nanosheets at carbon cloth (Bi2S3 NFNS@CC) are synthesized as anode capable to operate at negative (−1.3 to 0 V) potential window. The 2.6 V ASC is constructed by K0.46MnO2 NSAs@CC as cathode and Bi2S3 NFNS@CC as an anode (K0.46MnO2 NSAs@CC//Bi2S3 NFNS@CC). K0.46MnO2 NSAs@CC//Bi2S3 NFNS@CC as ASC is presenting excellent energy density of ∼72 Wh kg−1 on top of outstanding cycle performance and rate capability compatible with the earlier reported MnO2-based ASCs. This work is elaborating the new guidelines for novel electrode materials scheme and possibilities to achieve broaden potential windows capable to be utilized in practical devices.

Enhancing the stability of NiFe-layered double hydroxide nanosheet array for alkaline seawater oxidation by Ce doping

Electrocatalytic hydrogen production from seawater holds enormous promise for clean energy generation. Nevertheless, the direct electrolysis of seawater encounters significant challenges due to poor anodic stability caused by detrimental chlorine chemistry. Herein, we present our recent discovery that the incorporation of Ce into NiFe layered double hydroxide nanosheet array on Ni foam (Ce-NiFe LDH/NF) emerges as a robust electrocatalyst for seawater oxidation. During the seawater oxidation process, CeO2 is generated, effectively repelling Cl− and inhibiting the formation of ClO−, resulting in a notable enhancement in the oxidation activity and stability of alkaline seawater. The prepared Ce-NiFe LDH/NF requires only overpotential of 390 mV to achieve the current density of 1 A cm−2, while maintaining long-term stability for 500 h, outperforming the performance of NiFe LDH/NF (430 mV, 150 h) by a significant margin. This study highlights the effectiveness of a Ce-doping strategy in augmenting the activity and stability of materials based on NiFe LDH in seawater electrolysis for oxygen evolution.

Hydrophilic 1T-WS2 Nanosheet Arrays toward Conductive Textiles for High-Efficient and Continuous Hydroelectric Generation and Storage.

Flexible hydroelectric generators (HEGs) are promising self-powered devices that spontaneously derive electrical power from moisture. However, achieving the desired compatibility between a continuous operating voltage and superior current density remains a significant challenge. Herein, a textile-based van der Waals heterostructure is rationally designed between conductive 1T phase tungsten disulfide@carbonized silk (1T-WS2@CSilk) and carbon black@cotton (CB@Cotton) fabrics with an asymmetric distribution of oxygen-containing functional groups, which enhances the proton concentration gradients toward high-performance wearable HEGs. The vertically staggered 1T-WS2 nanosheet arrays on the CSilk fabric provide abundant hydrophilic nanochannels for rapid carrier transport. Furthermore, the moisture-induced primary battery formed between the active aluminum (Al) electrode and the conductive textiles introduces the desired electric field to facilitate charge separation and compensate for the decreased streaming potential. These devices exhibit a power density of 21.6µWcm-2, an open-circuit voltage (Voc) of 0.65V sustained for over 10000s, and a current density of 0.17mAcm-2. This performance makes them capable of supplying power to commercial electronics and human respiratory monitoring. This study presents a promising strategy for the refined design of wearable electronics.

Plasma-Engineered CeOx Nanosheet Array with Nitrogen-Doping and Porous Architecture for Efficient Electrocatalysis.

Surface engineering has been proved efficient and universally applicable in improving the performance of CeO2 in various fields. However, previous approaches have typically required high-temperature calcination or tedious procedures, which makes discovery of a moderate and facile modification approach for CeO2 an attractive subject. In this paper, porous CeO2 nanosheets with effective nitrogen-doping were synthesized via a low-temperature NH3/Ar plasma treatment and exhibited boosted hydrogen evolution reaction performance with low overpotential (65 mV) and long-term stability. The mechanism of the elevated performance was investigated by introducing Ar-plasma-treated CeO2 with no nitrogen-doping as the control group, which revealed the dominant role of nitrogen-doping by providing abundant active sites and improving charge transfer characteristics. This work illuminates further investigations into the surface engineering methodologies boosted by plasma and the relative mechanism of the structure-activity relationship.

Advanced 3D hierarchical composite electrode materials for supercapacitors: Biomass derived carbon doped CoMoO4@NiCo2O4

Carbon-doped CoMoO4@NiCo2O4 on nickel foam (C-CoMoO4@NiCo2O4@Ni foam) electrode is prepared by two-step hydrothermal method. Phyllanthus reticulates extract is used as carbon source and reducing agent for preparation of CoMoO4@NiCo2O4. The XRD and FE-SEM analyses have confirmed the formation of phases and the hierarchical structure of this electrode. Moreover, this C-CoMoO4@NiCo2O4@Ni foam electrode has been directly employed in supercapacitor applications. Impressively, it exhibits a high specific capacitance of 3130 F g−1 at a current density of 1 A g−1, surpassing the performance of both C-CoMoO4@Ni foam (2482 F g−1) and C-NiCo2O4@Ni foam electrodes (1884 F g−1). Remarkably, the C-CoMoO4@NiCo2O4@Ni foam electrode maintains good rate performance, with a 60 % capacity retention after 10,000 cycles at a current density of 100 A g−1. This outstanding performance can be attributed to the distorted array of CoMoO4 nanosheets and NiCo2O4 nanoflakes, which significantly enhance the exposure of active sites and provide a larger surface area for redox reactions. In summary, the C-CoMoO4@NiCo2O4@Ni foam electrode offers exceptional specific capacity, long-term cycling stability, and excellent rate performance, making it a promising choice for various energy storage applications, including supercapacitors.

Fe(OH)x modified ultra-small Ru nanoparticles for highly efficient hydrogen evolution reaction and its application in water splitting

Developing highly active electrocatalysts for overall water splitting is of remarkable significance for industrial production of H2. Herein, exceptionally active Fe(OH)x modified ultra-small Ru nanoparticles on Ni(OH)2 nanosheets array (Fe(OH)x-Ru/Ni(OH)2) for both hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) are reported. The Fe(OH)x-Ru/Ni(OH)2 nanosheets array prepared with Fe/Ru molar ratio of 5 only requires extremely low overpotentials of 61, 127 and 170 mV to reach current densities of 100, 500 and 800 mA cm−2 in 1 M KOH, respectively, exceeding Pt/C catalyst (75, 160 and 177 mV). Meanwhile, the Fe(OH)x/Ni(OH)2 nanosheets array derived from Fe(OH)x-Ru/Ni(OH)2 exhibits excellent OER activity. It gains current densities of 100, 500 and 800 mA cm−2 at considerably low overpotentials of 265, 285 and 296 mV, respectively, much lower than those of RuO2 and most reported electrocatalysts. The introduction of Fe(OH)x significantly improves the HER activity of Ru nanoparticles by tunning the electronic structure and forming interfaces between Ru and Fe(OH)x. Dramatically, the integrated alkaline electrolyzer based on Fe(OH)x-Ru/Ni(OH)2 and Fe(OH)x/Ni(OH)2 nanosheets array pair just needs 1.649 V to yield a current density up to 500 mA cm−2, exceeding most reported water-splitting electrocatalysts. The strategy reported in this work can be facilely extended to prepare other similar Ru based materials and their derivatives with outstanding catalytic performance for water splitting.

Self-supported Pt nanoparticles-NiFeP nanosheets arrays nanohybrid with hydrophilic surface towards urea electrolysis

Urea-assisted water electrolysis is a clean, sustainable, and energy-saving method towards hydrogen production. However, the development of earth-abundant, stable, and highly active bifunctional catalysts towards urea electrolysis is still a significant technical challenge. Herein, the highly dispersed Pt nanoparticles decorated NiFeP nanosheets arrays on nickel foam (Pt-NiFeP/NF) electrode is rationally designed, which combines the advantages of superhydrophilic interface, ultrathin nanostructure and open three-dimensional (3D) architecture. Consequently, Pt-NiFeP/NF displays a remarkable electroactivity towards both hydrogen evolution reaction (HER) and urea electrooxidation reaction (UEOR), which only needs the overpotential of 32 mV to achieve the current density of 10 mA cm−2 towards HER, and drives a current density of 50 mA cm−2 at 1.38 V towards UEOR. More importantly, the urea electrolysis system assembled with Pt-NiFeP/NF only requires a cell voltage of 1.41 V to achieve a current density of 100 mA cm−2, much lower than the traditional water electrolysis (1.94 V). This work promotes the application of Pt nanoparticles decorated bimetallic phosphides as a bifunctional catalyst towards urea-rich wastewater treatment and green electrochemical hydrogen production.

In-situ Ni-doped V-MOF ultra-thin nanosheet arrays on Ni foam for high-performance hybrid supercapacitors

Bimetallic organic frameworks possess distinctive structural and component benefits that make them essential materials for energy storage devices with outstanding capabilities. Here, ultra-thin 2D VNi-MOF nanosheet arrays (NSAs) have been in-situ grown on nickel foam (NF) which served as both the current collector and the Ni source by pretreatment and one-step solvothermal method and used as an efficient electrode material for high performance supercapacitors. Benefiting from its ultra-thin 2D NSAs structure and the synergy of bimetallic ions, the VNi-MOF NSAs/NF exhibits a high specific capacity performance (516.5 C g−1 at 1 A g−1) and outstanding cycling stability (85.6 % capacity retention over 12, 000 cycles at 20 A g−1). Battery-type VNi-MOF NSAs/NF and capacitive-type AC are integrated to assemble a HSC. The prototype HSC achieves a remarkably high energy density of 43 Wh kg−1 (at 800 W kg−1), which demonstrates the great potential of VNi-MOF (bimetallic organic framework) as a HSC electrode.

Dopant-Induced Charge Redistribution on the 3D Sponge-like Hierarchical Structure of Quaternary Metal Phosphides Nanosheet Arrays Derived from Metal-Organic Frameworks for Natural Seawater Splitting.

Dopant-induced electron redistribution on transition metal-based materials has long been considered an emerging new electrocatalyst that is expected to replace noble-metal-based electrocatalysts in natural seawater electrolysis; however, their practical applications remain extremely daunting due to their sluggish kinetics in natural seawater. In this work, we developed a facile strategy to synthesize the 3D sponge-like hierarchical structure of Ru-doped NiCoFeP nanosheet arrays derived from metal-organic frameworks with remarkable hydrogen evolution reaction (HER) performance in natural seawater. Based on experimental results and density functional theory calculations, Ru-doping-induced charge redistribution on the surface of metal active sites has been found, which can significantly enhance the HER activity. As a result, the 3D sponge-like hierarchical structure of Ru-NiCoFeP nanosheet arrays achieves low overpotentials of 52, 149, and 216 mV at 10, 100, and 500 mA cm-2 in freshwater alkaline, respectively. Notably, the electrocatalytic activity of the Ru-NiCoFeP electrocatalyst in simulated alkaline seawater and natural alkaline seawater is nearly the same as that in freshwater alkaline. This electrocatalyst exhibits superior catalytic properties with outstanding stability under a high current density of 85 mA cm-2 for more than 100 h in natural seawater, which outperforms state-of-the-art 20% Pt/C at high current density. Our work provides valuable guidelines for developing a low-cost and high-efficiency electrocatalyst for natural seawater splitting.

Application of 3D hierarchical porous NiCo-spinel nanosheet array for enhancement of synergistic activation of peroxymonosulfate: Degradation, Intermediates, mechanism and degradation pathway of tetracycline

The rational design of the morphology and structure of bimetallic-based heterogeneous Fenton-like catalyst derived from metal-organic-frameworks (MOFs) for peroxymonosulfate (PMS) activation via a non-radical pathway is attractive but challenging. Herein, a spinel-type 3D hierarchical porous NiCo2O4 nanosheet array for the activation of PMS is rationally designed by surfactant-assisted interfacial engineering. The experimental results showed that the NiCo2O4/PMS system demonstrated remarkable oxidative degradation of tetracycline (TC) through 1O2 attack and electron transfer process. In literature, it was thought that the PMS activation process in above system is dominated by radical pathway. In this work, we employ surfactant modified-nanostructure engineering to design hierarchical mesoporous nanosheet array structures and combined them with intrinsic bimetallic synergy to enhance catalytic activity, and interestingly the strategy transformed the PMS activation pathway into a nonradical (1O2 and electron transfer)-dominated process. This is benefit from the favorable morphological and electronic structure of the designed catalysts to facilitate mass transfer and electron transfer processes. The system also possessed a broad spectrum for degrading other typical contaminants, and was effective in tolerating actual water matrix and pH changes, as well as resisting interference from anions and organic matter. Furthermore, the robust stability of the structure and catalytic activity make it promising for practical water treatment. It can be expected that this proposal will provide insights for the delicate structural design and the understanding of its PMS activation mechanism of bimetallic-based Fenton-like catalysts, as well as for the efficient degradation of emerging organic pollutants.

Ru doping and interface engineering synergistically boost the electrocatalytic performance of a WP/WP2 nanosheet array for an efficient hydrogen evolution reaction.

The surface electronic structure and morphology of catalysts have a crucial impact on the electrocatalytic hydrogen evolution reaction performance. This work reports on the fabrication of a Ru-doped WP/WP2 heterojunction nanosheet array electrode via a one-step phosphating treatment of a Ru-doped WO3 precursor. Benefitting from the large electrochemical active surface of nanosheet arrays, rich WP/WP2 heterojunction interface, and trace Ru atom doping, the catalyst has a fairly low overpotential of 58.0 mV at 10 mA cm-2 and a Tafel slope of 50.71 mV dec-1 in acid solution toward the electrocatalytic HER. Further, theoretical calculations unveil that Ru atom doping and interface effect synergistically optimized the electronic structure of the catalyst and hence weakened the adsorption capacity of the catalyst surface toward hydrogen (H), which lowered the Gibbs free energy (ΔGH*) and consequently effectively improved the HER performance. This work may open new avenues for developing advanced nanoarray electrodes with efficient electrochemical energy conversion.

Dual cation-modified hierarchical nickel hydroxide nanosheet arrays as efficient and robust electrocatalysts for the urea oxidation reaction.

The rational modification of electronic structures to create catalytically active sites has been proved to be a promising strategy to efficiently facilitate the urea oxidation reaction (UOR). Herein, a well-defined nanosheet arrays catalyst of Ni(OH)2 doped with dual cations of Co and Mn on Ni foam (NF) (Co/Mn-Ni(OH)2) is synthesized through a simple hydrothermal process. Benefiting from the advantages of unique structures and modified binding strengths, it is found experimentally that the obtained Co/Mn-Ni(OH)2 catalyst only requires a potential of 1.38 V to deliver a current density of 100 mA cm-2 and exhibits a small Tafel slope of 35 mV dec-1, outperforming single-component-incorporated Ni(OH)2. Moreover, the catalyst has shown excellent stability for 25 h at a current density of 50 mA cm-2. Additionally, first-principles calculations demonstrate that the co-incorporation of Co and Mn remarkably lowers the adsorption barrier of CO(NH2)2* on the catalyst surface, and accelerates the dissociation of the CO(NH2)2* intermediate into CO* and NH* intermediates, which synergistically improve the UOR reaction kinetics. This work provides a generic paradigm for designing advanced and effective catalysts toward the UOR.

Electrochemical PET recycling to formate through ethylene glycol oxidation on Ni-Co-S nanosheet arrays

Plastics have become an integral part of modern society due to their excellent mechanical properties, lightweight, chemical stability and low cost. However, their continuous production and use worldwide have resulted...

Constructing Ni species-incorporated CoP@N-doped carbon nanosheet arrays for efficient self-powered hydrazine-assisted seawater electrolysis

Ni species-incorporated CoP nanosheet arrays encapsulated in N-doped carbon layers that exhibit excellent HER, HzOR and hydrazine-assisted seawater splitting activities were synthesized, and a multi-powered hydrogen production system was proposed.

ZnFe2O4 nanosheet array: a highly efficient electrocatalyst for ambient ammonia production via nitrite reduction

ZnFe2O4 nanosheet arrays on nickel foam (ZnFe2O4/NF) act as a high-performance electrocatalyst for the electroreduction of NO2− to NH3.

MnOx-decorated MOF-derived nickel-cobalt bimetallic phosphide nanosheet arrays for overall water splitting.

Exploring non-noble metal dual-functional electrocatalysts with high activity and stability for water splitting is highly desirable. In this study, using zeolitic imidazolate framework-L (ZIF-L) nanoarrays as the precursor, manganese oxide-decorated porous nickel-cobalt phosphide nanosheet arrays have been prepared on nickel foam (denoted as MnOx/NiCoP/NF) through cation etching, phosphorization and electrodeposition, which are utilized as an efficient dual-functional electrocatalyst for overall water splitting. The hierarchical porous nanosheet arrays provide abundant active sites for the electrochemical process, while the MnOx modification induces strong interfacial interaction, benefiting charge transfer. Thus, the MnOx/NiCoP/NF exhibits excellent electrocatalytic activity toward the hydrogen evolution reaction (HER, overpotential of 93 mV at 10 mA cm-2), oxygen evolution reaction (OER, overpotential of 240 mV at 10 mA cm-2) and overall water splitting (cell voltage of 1.59 V at 10 mA cm-2). Furthermore, it shows superior stability during continuous overall water splitting for 200 h. This work provides a simple and effective approach for developing efficient non-noble metal dual-functional catalysts for overall water splitting.

Self-supported FeCoNiCuP high-entropy alloy nanosheet arrays for efficient glycerol oxidation and hydrogen evolution in seawater electrolytes

Self-supported FeCoNiCuP high entropy alloy nanosheet arrays electrocatalyst was developed for highly efficient glycerol oxidation to formate and hydrogen evolution in seawater electrolytes.

Porous VN nanosheet arrays on MXene carbon fibers for flexible supercapacitors.

VN usually has poor rate performance and cycle stability. In this work, porous VN nanosheet arrays were prepared on carbon nanofibers embedded with Ti3C2Tx nanosheets by electrospinning and chemical vapor deposition. The 3D network accelerates the transfer of electrons and electrolyte ions, prevents the aggregation of VN and the self-stacking of MXene, and enhances cycle stability. The solid-state flexible device comprising Co3O4, MXCF@VN, and KOH/PVA exhibits exceptional energy densities of 83.95 W h kg-1 and robust cycling stability (82.8% retention after 20 000 cycles).

Surface engineering assisted CoNiP nanosheet arrays for electrochemical overall water splitting

Electrochemical overall water splitting is a green, environmentally friendly, and efficient hydrogen production method that involves two half-reactions: the oxygen evolution reaction (OER) and the hydrogen evolution reaction (HER).

Improved ZnWO4@NiCo2O4 core-shell nanosheet arrays with regulatory interfaces and electronic redistribution.

ZnWO4@NiCo2O4 core-shell nanosheet array composites are synthesized on nickel foam via a two-step hydrothermal method. The optimal conditions, including a Ni(NO3)2·6H2O to Co(NO3)2·6H2O molar ratio of 2 : 1, 12 hours reaction time, and 120 °C temperature, yield a specific capacitance of 875 C g-1 at 1 A g-1. The electrode also maintains 81.1% capacitance after 10 000 cycles. The material's performance is attributed to its core-shell structure, which enhances ion diffusion and electron transport. This study presents a viable approach for high-performance supercapacitor electrodes.