Highly Efficient CoFeP Nanoparticle Catalysts for Superior Oxygen Evolution Reaction Performance.

Developing effective and long-lasting electrocatalysts for oxygen evolution reaction (OER) is critical for increasing sustainable hydrogen production. This paper describes the production and characterization of CoFeP nanoparticles (CFP NPs) as high-performance electrocatalysts for OER. The CFP NPs were produced using a simple hydrothermal technique followed by phosphorization, yielding an amorphous/crystalline composite structure with improved electrochemical characteristics. Our results reveal that CFP NPs have a surprisingly low overpotential of 284 mV at a current density of 100 mA cm-2, greatly exceeding the precursor CoFe oxide/hydroxide (CFO NPs) and the commercial RuO2 catalyst. Furthermore, CFP NPs demonstrate exceptional stability, retaining a constant performance after 70 h of continuous operation. Post-OER characterization analysis revealed transformations in the catalyst, including the formation of cobalt-iron oxides/oxyhydroxides. Despite these changes, CFP NPs showed superior long-term stability compared to native metal oxides/oxyhydroxides, likely due to enhanced surface roughness and increased active sites. This study proposes a viable strategy for designing low-cost, non-precious metal-based OER catalysts, which will help advance sustainable energy technology.

Phosphorus-Doping Enables the Superior Durability of a Palladium Electrocatalyst towards Alkaline Oxygen Reduction Reactions.

The sluggish kinetics of oxygen reduction reactions (ORRs) require considerable Pd in the cathode, hindering the widespread of alkaline fuel cells (AFCs). By alloying Pd with transition metals, the oxygen reduction reaction's catalytic properties can be substantially enhanced. Nevertheless, the utilization of Pd-transition metal alloys in fuel cells is significantly constrained by their inadequate long-term durability due to the propensity of transition metals to leach. In this study, a nonmetallic doping strategy was devised and implemented to produce a Pd catalyst doped with P that exhibited exceptional durability towards ORRs. Pd3P0.95 with an average size of 6.41 nm was synthesized by the heat-treatment phosphorization of Pd nanoparticles followed by acid etching. After P-doping, the size of the Pd nanoparticles increased from 5.37 nm to 6.41 nm, and the initial mass activity (MA) of Pd3P0.95/NC reached 0.175 A mgPd-1 at 0.9 V, slightly lower than that of Pd/C. However, after 40,000 cycles of accelerated durability testing, instead of decreasing, the MA of Pd3P0.95/NC increased by 6.3% while the MA loss of Pd/C was 38.3%. The durability was primarily ascribed to the electronic structure effect and the aggregation resistance of the Pd nanoparticles. This research also establishes a foundation for the development of Pd-based ORR catalysts and offers a direction for the future advancement of catalysts designed for practical applications in AFCs.

Facile Synthesis of PtP2 Nanocrystals as Highly Active Electrocatalysts for Methanol Oxidation.

Although significant efforts have been made in the past few decades, the development of affordable, durable, and effective electrocatalysts for direct methanol fuel cells (DMFCs) remains a formidable challenge. Herein, we present a facile and efficient phosphorization approach for synthesizing PtP2 intermetallic nanocrystals and utilize them as electrocatalysts in the methanol oxidation reaction (MOR). Impressively, the synthesized PtP2 nanocatalysts exhibit a mass activity of 2.14 mA µg-1 and a specific activity of 6.28 mA cm-2, which are 5.1 and 9.5 times higher than those achieved by the current state-of-the-art commercial Pt/C catalyst, respectively. Moreover, the PtP2 nanocatalysts demonstrate improved stability toward acidic MOR by retaining 92.1% of its initial mass activity after undergoing 5000 potential cycles, far surpassing that of the commercial Pt/C (38%). Further DMFC tests present a 2.7 times higher power density than that of the commercial Pt/C, underscoring their potential for application in methanol fuel cells. Density functional theory calculations suggest that the accelerated MOR kinetics and improved CO tolerance on PtP2 can be attributed to the attenuated binding strength of CO intermediates and the enhanced stability due to strong Pt-P interaction. To our knowledge, this is the first report identifying the MOR performance on PtP2 intermetallic nanocrystals, highlighting their potential as highly active and stable nanocatalysts for DMFCs.

Constructing Chainmail-Structured CoP/C Nanospheres as Highly Active Anodic Electrocatalysts for Oxygen Evolution Reaction.

Constructing highly active and noble metal-free electrocatalysts is significant for the anodic oxygen evolution reaction (OER). Herein, uniform carbon-coated CoP nanospheres (CoP/C) are developed by a direct impregnation coupling phosphorization approach. Importantly, CoP/C only takes a small overpotential of 230 mV at the current density of 10 mA cm-2 and displays a Tafel slope of 56.87 mV dec-1. Furthermore, the intrinsic activity of CoP/C is 21.44 times better than that of commercial RuO2 under an overpotential of 260 mV. In situ Raman spectroscopy studies revealed that a large number of generated Co-O and Co-OH species could facilitate the *OH adsorption, effectively accelerating the reaction kinetics. Meanwhile, the carbon shell with a large number of mesoporous pores acts as the chainmail of CoP, which could improve the active surface area of the catalyst and prevent the Co sites from oxidative dissolution. This work provides a facile and effective reference for the development of highly active and stable OER catalysts.

P-bridged Fe-X-Co coupled sites in hollow carbon spheres for efficient hydrogen generation.

Non-precious metals have shown attractive catalytic prospects in hydrogen production from ammonia borane hydrolysis. However, the sluggish reaction kinetics in the hydrolysis process remains a challenge. Herein, P-bridged Fe-X-Co coupled sites in hollow carbon spheres (Fe-CoP@C) has been synthesized through in situ template solvothermal and subsequent surface-phosphorization. Benefiting from the optimized electronic structure induced by Fe doping to enhance the specific activity of Co sites, bimetallic synergy and hollow structure, the as-prepared Fe-CoP@C exhibits superior performances with a turnover frequency (TOF) of 183.5 min-1, and stability of over 5 cycles for ammonia borane hydrolysis, comparable to noble metal catalysts. Theoretical calculations reveal that the P-bridged Fe-X-Co coupled sites on the Fe-CoP@C catalyst surfaces is beneficial to adsorb reactant molecules and reduce their reaction barrier. This strategy of constructing hollow P-bridged bimetallic coupled sites may open new avenues for non-precious metal catalysis.

Enhancing Electrochemical Non-Enzymatic Dopamine Sensing Based on Bimetallic Nickel/Cobalt Phosphide Nanosheets.

In this study, the successful synthesis of bimetallic nickel/cobalt phosphide nanosheets (Ni-Co-P NSs) via the hydrothermal method and the subsequent high-temperature phosphorization process were both confirmed. Ni-Co-P NSs exhibited excellent electrocatalytic activity for the electrochemical non-enzymatic DA sensing. The surface morphologies and physicochemical properties of Ni-Co-P NSs were characterized by atomic force microscopy (AFM), field-emission scanning (FESEM), field-emission transmission electron microscopy (FETEM), and X-ray diffraction (XRD). Further, the electrochemical performance was evaluated by cyclic voltammetry (CV) and differential pulse voltammetry (DPV). The metallic nature of phosphide and the synergistic effect of Ni/Co atoms in Ni-Co-P NSs provided abundant catalytic active sites for the electrochemical redox reaction of DA, which exhibited a remarkable consequence with a wide linear range from 0.3~50 µM, a high sensitivity of 2.033 µA µM-1 cm-2, a low limit of detection of 0.016 µM, and anti-interference ability. As a result, the proposed Ni-Co-P NSs can be considered an ideal electrode material for the electrochemical non-enzymatic DA sensing.

Oxygen-doped NiCoP derived from Ni-MOFs for high performance asymmetric supercapacitor.

Oxygen doping strategy is one of the most effective methods to improve the electrochemical properties of nickel-cobalt phosphide (NiCoP)-based capacitors by adjusting its inherent electronic structure. In this paper, O-doped NiCoP microspheres derived from porous nanostructured nickel metal-organic frameworks (Ni-MOFs) were constructed through solvothermal method followed by phosphorization treatment. The O-doping concentration has a siginificant influence on the rate performance and cycle stability. The optimized O-doped NiCoP electrode material shows a specific capacitance of 632.4 F-g-1at 1 A-g-1and a high retention rate of 56.9% at 20 A g-1. The corresponding NiCoP-based asymmetric supercapacitor exhibits a high energy density of 30.1 Wh kg-1when the power density is 800.9 W kg-1, and can still maintain 82.1% of the initial capacity after 10 000 cycles at 5 A g-1.

Phosphate-modified cobalt silicate hydroxide with improved oxygen evolution reaction.

Oxygen Evolution Reaction (OER) has gained significant attention due to its crucial role in renewable energy systems. The quest for efficient and low-cost OER catalysts remains a challenge of significant interest and importance. In this work, phosphate-incorporated cobalt silicate hydroxide (denoted as CoSi-P) is reported as a potential electrocatalyst for OER. The researchers first synthesized hollow spheres of cobalt silicate hydroxide Co3(Si2O5)2(OH)2 (denoted as CoSi) using SiO2 spheres as a template through a facile hydrothermal method. Phosphate (PO43-) was then introduced to layered CoSi, leading to the reconstruction of the hollow spheres into sheet-like architectures. As expected, the resulting CoSi-P electrocatalyst demonstrated low overpotential (309 mV at 10 mA·cm-2), large electrochemical active surface area (ECSA), and low Tafel slope. These parameters outperform CoSi hollow spheres and cobaltous phosphate (denoted as CoPO). Moreover, the catalytic performance achieved at 10 mA cm-2 is comparable or even better than that of most transition metal silicates/oxides/hydroxides. The findings indicate that the incorporation of phosphate into the structure of CoSi can enhance its OER performance. This study not only provides a non-noble metal catalyst CoSi-P but also demonstrates that the incorporation of phosphates into transition metal silicates (TMSs) offers a promising strategy for the design of robust, high-efficiency, and low-cost OER catalysts.

In Situ Construction of Heterostructured Co3O4/CoP Nanoflake Arrays on Carbon Cloth as Binder-Free Anode for High-Performance Lithium-Ion Batteries.

Cobalt oxide (Co3O4) is regarded as the anode material for lithium-ion batteries (LIBs) with great research value owing to its environmental friendliness and exceptional theoretical capacity. However, the low intrinsic conductivity, poor electrochemical kinetics, and unsatisfactory cycling performance severely limit its practical applications in LIBs. The construction of a self-standing electrode with heterostructure by introducing a highly conductive cobalt-based compound is an effective strategy to solve the above issues. Herein, Co3O4/CoP nanoflake arrays (NFAs) with heterostructure are constructed skillfully directly grown on carbon cloth (CC) by in situ phosphorization as an anode for LIBs. Density functional theory simulation results demonstrate that the construction of heterostructure greatly increases the electronic conductivity and Li ion adsorption energy. The Co3O4/CoP NFAs/CC exhibited an extraordinary capacity (1490.7 mA h g-l at 0.1 A g-l) and excellent performance at high current density (769.1 mA h g-l at 2.0 A g-l), as well as remarkable cyclic stability (451.3 mA h g-l after 300 cycles with a 58.7% capacity retention rate). The reasonable construction of heterostructure can promote the interfacial ion transport, significantly enhance the adsorption energy of lithium ions, improve the conductivity of Co3O4 electrode material, promote the partial charge transfer throughout the charge and discharge cycles, and enhance the overall electrochemical performance of the material.

Self-supported Ni2P/NiMoP2 bimetallic phosphide with strong electronic interaction for efficient overall water splitting.

Electronic regulation via interface engineering is recognized as an attractive strategy for boosting electrocatalytic activity. In this work, a self-supported heterostructure electrocatalyst is explored by a feasible hydrothermal-pyrolysis strategy, in which Ni2P nanoparticles are anchored on NiMoP2 nanosheet arrays grown on carbon cloth (Ni2P/NiMoP2/CC). Benefitting from the nanosheet array architecture and the synergy effect between the Ni2P and NiMoP2, the as-prepared Ni2P/NiMoP2/CC manifests highly efficient activity and stability toward both hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). Density functional theory calculations further indicates that the heterointerface in Ni2P/NiMoP2/CC enable optimized interface electron structure and reduce the activation barriers for intermediates, improving the intrinsic electrocatalytic activity. Remarkably, the Ni2P/NiMoP2/CC||Ni2P/NiMoP2/CC electrolyzer affords 10 mA cm-2 at a low voltage of 1.59 V, outperforming its monometallic phosphides counterparts and most of transition metal-based bifunctional electrocatalysts. The electrolyser was powered by a solar cell to produce H2 and O2 simultaneously, indicating its potential application in solar-to-hydrogen conversion.

N doped FeP nanospheres decorated carbon matrix as an efficient electrocatalyst for durable lithium-sulfur batteries.

Rational design and synthesis of multifunctional electrocatalysts with high electrochemical activity and low cost are significantly important for new-generation lithium-sulfur (Li-S) batteries. Herein, N-doped FeP nanospheres decorated N doped carbon matrix is successfully synthesized by facile one-pot pyrolysis and in-situ phosphorization technique to mitigate the conversion kinetics and suppress the shuttle effect. The large specific surface area with mesopores can incorporate up to 81.5% sulfur, with the conductive carbon and nitrogen co-matrix providing Li+/e- passage and fastening the redox kinetics. The remarkable adsorption properties and the electrocatalytic activity through physical confinement and chemical immobilization is thoroughly verified. Consequently, the FeP/CN@S deliver a high reversible capacity of 1183 mAh g-1 at 0.1C compared to Co/P/CN@S (961 mAh g-1); whereas, at 1C, a negligible decay rate of 0.04% is observed for 1000 cycles, possessing outstanding cycling stability and rate capability. Hence, the cost-effective in-situ phosphorization strategy to synthesize FeP/CN@S as an efficient nanoreactor is constructive to be applied in Li-S batteries.

Partial Phosphorization: A Strategy to Improve Some Performance(s) of Thiolated Metal Nanoclusters Without Notable Reduction of Stability.

Thiolates endow metal nanoclusters with stability while sometimes inhibit the catalytic activity due to the strong M-S interaction (M: metal atom). To improve the catalytic activity and keep the stability to some extent, one strategy is the partial phosphorization of thiolated metal nanoclusters. This is demonstrated by successful partial phosphorization of Au23 (SC6 H11 )16 and by revealing that the products Au22 (SC6 H11 )14 (PPh3 )2 and Au22 (SC6 H11 )12 (PPh3 )4 , with varied degree of phosphorization, both show excellent activity in the photocatalytic oxidation of thioanisole without notable reduction of stability. Furthermore, Au22 (SC6 H11 )12 (PPh3 )4 exhibits better photoluminescence performance than the mother nanocluster Au23 (SC6 H11 )16 , indicating that partial phosphorization can also improve some other performance(s) except for the catalytic performance. The intermediates Au22-x Cux (SC6 H11 )12 (PPh3 )4 (x=1, 2) in the transformation from Au23 (SC6 H11 )16 (Au22 (SC6 H11 )14 (PPh3 )2 ) to Au22 (SC6 H11 )12 (PPh3 )4 were captured and identified by mass spectrometry and single crystal X-ray diffraction, which throws light on the understanding of the non-alloyed anti-galvanic reaction.

Mo,Fe-codoped metal phosphide nanosheets derived from Prussian blue analogues for efficient overall water splitting.

Designing non-precious electrocatalysts with multiple active centers and durability toward overall water splitting is of great significance for storing renewable energy. This study reports a low-cost Mo, Fe codoped NiCoPx electrocatalysts derived from Co-Fe Prussian blue analogue and following phosphorization process. Benefitted from the optimized electronic configuration, hierarchical structure and abundant active sites, the Mo,Fe-NiCoPx/NF electrode has shown competitive oxygen evolution reaction (ƞ10 = 197 mV) and hydrogen evolution reaction performance (ƞ10 = 99 mV) when the current density is 10 mA cm-2 in 1 M KOH solution. Moreover, the integrated water splitting device assembled by Mo,Fe-NiCoPx/NF as both anode and cathode only needs a voltage of 1.545 V to reach 10 mA cm-2. Density functional theory results further confirm that the Mo, Fe codoped heterostructure can synergistically optimize the d-band center and Gibbs free energy during electrocatalytic processes, thus accelerating the kinetics of electrochemical water splitting. This work demonstrates the importance of rational combination of metal doping and interface engineering for advanced catalytic materials.

General metal-organic framework-derived strategy to synthesize yolk-shell carbon-encapsulated nickelic spheres for sodium-ion batteries.

Transition-metal compounds have attracted enormous attention as potential energy storage materials for their high theoretical capacity and energy density. However, the most present transition-metal compounds still suffer from severe capacity decay and limited rate capability due to the lack of robust architectures. Herein, a general metal-organic framework-derived route is reported to fabricate hierarchical carbon-encapsulated yolk-shell nickelic spheres as anode materials for sodium-ion batteries. The nickelic metal-organic framework (Ni-MOF) precursors can be in situ converted into hierarchical carbon-encapsulated Ni2P (Ni2P/C), NiS2 (NiS2/C) and NiSe2 (NiSe2/C) by phosphorization, sulfuration, and selenation reaction, respectively, and maintain their yolk-shell sphere-like morphology. The as-synthesized Ni2P/C sample can deliver much lower polarization and discharge platform, smaller voltage gap, and faster kinetics in comparison with that of the other two counterparts, and thus achieve higher initial specific capacity (3222.1/1979.3 mAh g-1) and reversible capacity of 765.4 mAh g-1 after 110 cycles. This work should provide new insights into the phase and structure engineering of carbon-encapsulated transition-metal compound electrodes via MOFs template for advanced battery systems.

Synthesis of Bimetallic Ni-Co Phosphide Nanosheets for Electrochemical Non-Enzymatic H2O2 Sensing.

NiCoP nanosheets (NSs) were successfully synthesized using the hydrothermal and high-temperature phosphorization process. The obtained NiCoP NSs were immobilized on a glassy carbon electrode (GCE) and used to construct a novel sensing platform for electrochemical non-enzymatic H2O2 sensing. Physicochemical characteristics of NiCoP NSs were obtained by field-emission scanning electron microscopy (FESEM), field-emission transmission electron microscope (FETEM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). In addition, the electrochemical properties of NiCoP NSs were obtained by cyclic voltammetry (CV) and chronoamperometry (CA) towards the non-enzymatic detection of H2O2. FESEM and FETEM images provided a morphological insight (the unique nanosheets morphology of NiCoP) that could expose more active sites to promote mass/charge transport at the electrode/electrolyte interface. XRD and XPS results also confirmed the crystalline nature of the NiCoP nanosheets and the coexistence of multiple transitional metal oxidation states in NiCoP nanosheets. These unique physicochemical characteristics had a degree of contribution to ensuring enhancement in the electrochemical behavior. As a result, the synthesized NiCoP NSs composed of intercalated nanosheets, as well as the synergistic interaction between bimetallic Ni/Co and P atoms exhibited excellent electrocatalytical activity towards H2O2 electroreduction at neutral medium. As the results showed, the electrochemical sensing based on NiCoP NSs displayed a linear range of 0.05~4 mM, a sensitivity of 225.7 µA mM-1 cm-2, a limit of detection (LOD) of 1.190 µM, and good selectivity. It was concluded that NiCoP NSs-based electrochemical sensing might open new opportunities for future construction of H2O2 sensing platforms.

Controllable 3D Porous Ni Current Collector Coupled with Surface Phosphorization Enhances Na Storage of Ni3 S2 Nanosheet Arrays.

3D porous Ni is fabricated via an easily scalable electroless plating method using a dynamic template formed through in-situ hydrogen bubbles. The pore size in the range of several micrometers is controllable through adjusting the Ni2+ depositing rate and hydrogen bubbles releasing rate. The Ni3 S2 nanosheet arrays anode is then grown on the unique 3D porous Ni current collector followed by subsequent surface phosphorization. The tremendous interconnected pores and rich voids between the Ni3 S2 nanosheet arrays cannot only provide rapid transferring channels for Na+ , but also accommodate volumetric changes of the Ni3 S2 electrode during cycling, guaranteeing the integrity of the active material. In addition, the surface phosphorized layer enhances the electronic conductivity through providing an electron transport highway along the 3D Ni3 S2 , NiP2 layer, and 3D porous Ni current collector, and simultaneously stabilizes the electrode/electrolyte interphase as a protecting layer. Because of these merits, the phosphorized 3D porous Ni3 S2 (3D P-Ni3 S2 ) electrode is capable of delivering an ultra-stable capacity of 387.5 mAh g-1 at 0.1 A g-1 , and a high capacity retention of 85.3% even at a high current density of 1.6 A g-1 .

Hierarchically Assembling CoFe Prussian Blue Analogue Nanocubes on CoP Nanosheets as Highly Efficient Electrocatalysts for Overall Water Splitting.

Efficient and durable electrocatalysts are highly desirable for overall water splitting. Herein, a facile strategy is demonstrated to rationally construct CoFe Prussian blue analogues (PBA)@CoP cube-on-sheet hierarchical structure by etching reaction with intermediated CoO to form PBA nanocubes. Benefitting from the heterostructured engineering, the as-synthesized CoFe PBA@CoP presents remarkable electrocatalytic performance in 1.0 m KOH, only requiring overpotentials of 100 mV for hydrogen evolution reaction (HER) and 171 mV for oxygen evolution reaction (OER) to reach the 10 mA cm-2 current density with good stability. Extraordinarily enhanced electrocatalytic performance is ascribed to not only the rapid charge transfer of active species, but also the synergistic effect between each component to achieve tuned electronic structure and abundant electrocatalytic active sites. Especially, the assembled two-electrode cell using CoFe PBA@CoP as both cathode and anode delivers the current densities of 10 mA cm-2 at a relatively low cell voltage of 1.542 V, outperforming most of low-cost bifunctional electrocatalysts reported to date. The controllable and versatile strategy will open up an avenue to prepare hybrid films for advanced electrochemical energy storage and conversion.

Phosphorized CoNi2 S4 Yolk-Shell Spheres for Highly Efficient Hydrogen Production via Water and Urea Electrolysis.

Exploring earth-abundant electrocatalysts with excellent activity, robust stability, and multiple functions is crucial for electrolytic hydrogen generation. Porous phosphorized CoNi2 S4 yolk-shell spheres (P-CoNi2 S4 YSSs) were rationally designed and synthesized by a combined hydrothermal sulfidation and gas-phase phosphorization strategy. Benefiting from the strengthened Ni3+ /Ni2+ couple, enhanced electronic conductivity, and hollow structure, the P-CoNi2 S4 YSSs exhibit excellent activity and durability towards hydrogen/oxygen evolution and urea oxidation reactions in alkaline solution, affording low potentials of -0.135 V, 1.512 V, and 1.306 V (versus reversible hydrogen electrode) at 10 mA cm-2 , respectively. Remarkably, when used as the anode and cathode simultaneously, the P-CoNi2 S4 catalyst merely requires a cell voltage of 1.544 V in water splitting and 1.402 V in urea electrolysis to attain 10 mA cm-2 with excellent durability for 100 h, outperforming most of the reported nickel-based sulfides and even noble-metal-based electrocatalysts. This work promotes the application of sulfides in electrochemical hydrogen production and provides a feasible approach for urea-rich wastewater treatment.

Interfacial Control of NiCoP@NiCoP Core-Shell Nanoflake Arrays as Advanced Cathodes for Ultrahigh-Energy-Density Fiber-Shaped Asymmetric Supercapacitors.

Efficient improvement of the energy density and overall electrochemical performance of fiber-shaped asymmetric supercapacitors (FASCs) for practical applications in portable and wearable electronics requires highly electrochemically active materials and a rational design. Herein, two-step phosphorization (TSP) processes are performed to directly grow 3D well-aligned NiCoP@NiCoP (NCP@NCP TSP) nanoflake arrays (NFAs) on carbon nanotube fibers (CNTFs). Profiting from the metallic characteristics and excellent electrochemical performance of NiCoP and the hierarchical design of the core-shell heterostructure, the NCP@NCP TSP NFAs/CNTF hybrid electrode exhibits significantly improved electrochemical performance. The as-fabricated NCP@NCP TSP NFAs/CNTF electrode possesses an ultrahigh areal capacitance of 10 035 mF cm-2 at a current density of 1 mA cm-2 , with excellent rate capability and cycling stability. Furthermore, an FASC device with a maximum operating voltage of 1.6 V is assembled by adopting NCP@NCP TSP NFAs/CNTF as a positive electrode, hierarchical TiN@VN core-shell heterostructure nanowire arrays (NWAs)/CNTF as negative electrode, and KOH-PVA as a gel electrolyte. The FASC device exhibits a high areal capacitance of 430.4 mF cm-2 and an ultrahigh energy density of 51.02 mWh cm-3 . Thus, the rationally designed NiCoP@NiCoP electrode is a promising candidate for incorporation into next-generation wearable and portable energy-storage devices.

Direct epitaxial growth of nickel phosphide nanosheets on nickel foam as self-support electrode for efficient non-enzymatic glucose sensing.

Design and develop of cost-effective non-enzymatic electrode materials is of great importance for next generation of glucose sensors. In this work, we report a high-performance self-supporting electrode fabricated via direct epitaxial growth of nickel phosphide on Ni foam (Ni2P/NF) for nonenzymatic glucose sensors in alkaline solution. Under the optimal conditions, the uniform Ni2P nanosheets could be obtained with an average thickness of 80 nm, which provides sufficient active sites for glucose molecules. As a consequence, the Ni2P/NF electrode displays superior electrochemistry performances with a high sensitivity of 6375.1µA mM-1cm-2, a quick response about 1 s, a low detection limit of 0.14µM (S/N = 3), and good selectivity and specificity. Benefit from the strong interaction between Ni2P and NF, the Ni2P/NF electrode is also highly stable for long-term applications. Furthermore, the Ni2P/NF electrode is capable of analyzing glucose in human blood serum with satisfactory results, indicating that the Ni2P/NF is a potential candidate for glucose sensing in real life.