Synergistic Effects of the Ni3B Cocatalyst and N Vacancy on g-C3N4 for Effectively Enhanced Photocatalytic N2 Fixation.

The photocatalytic fixation of N2 is a promising technology for sustainable production of ammonia, while the unsatisfactory efficiency resulting from the low electron-transfer rate, narrow light absorption range, and limited active sites of the photocatalyst seriously hinder its application. Herein, we designed a noble metal-free Schottky junction photocatalyst constructed by g-C3N4 nanosheets with N vacancies (VN-CN) and metallic Ni3B nanoparticles (Ni3B/VN-CN) for N2 reduction to ammonia. The ammonia yield rate over the optimized Ni3B/VN-CN is 7.68 mM g-1 h-1, which is 6.7 times higher than that of pristine CN (1.15 mM g-1 h-1). The superior photocatalytic N2 fixation performance of Ni3B/VN-CN can be attributed not only to the formation of Schottky junctions between Ni3B and VN-CN, which facilitates the migration and separation of photogenerated electrons, but also to the incorporation of VN into g-C3N4, which enhances visible light absorption and improves electrical conductivity. More importantly, Ni3B nanoparticles can act as the cocatalyst, which provide more active sites for the adsorption and activation of N2, thereby improving the N2 reduction activity. This work provides an effective strategy of designing noble metal-free-based cocatalyst photocatalyst for sustainable and economic N2 fixation.

Synergistic Coupling of Charge Extraction and Sinking in Cu5FeS4/Ni3S2@NF for Photoassisted Electrocatalytic Oxygen Evolution.

Exploring low-cost and high-performance oxygen evolution reaction (OER) catalysts has attracted great attention due to their crucial role in water splitting. Here, a bifunctional Cu5FeS4/Ni3S2@NF catalyst was in situ formed on a nickel (Ni) foam toward efficient photoassisted electrocatalytic (P-EC) OER, which displays an ultralow overpotential of 260 mV at 30 mA cm-2 in alkaline solution, outperforming most previously reported Ni-based catalysts. It also shows great potential in degradation of antibiotics as an alternative anode reaction to OER owing to the prompt transfer of photogenerated holes. The photocurrent test and transient photovoltage spectroscopy indicate that the synergistic coupling of charge extraction and sinking effects in Cu5FeS4 and Ni3S2 is critical for boosting the OER activity via photoassistance. Electrochemical active surface area and electrochemical impedance spectroscopy tests further prove that the photogenerated electromotive force can effectively compensate the overpotential of OER. This work not only provides a good guidance for integrating photocatalysis and electrocatalysis, but also indicates the key role of synergistic extraction and utilization of photogenerated charge carriers in P-EC.

Synergistically Coupled CoMo/CoMoP Electrocatalyst for Highly Efficient and Stable Overall Water Splitting.

Finding reservoir-rich and efficient bifunctional electrocatalysts for water splitting is key to further sustainable energy development. Transition metal phosphides (TMPs) are extensively exploited as effective electrocatalysts, but the construction of strong coupling interfaces to improve catalytic performance by simple methods is still a bottleneck. Here, we designed and prepared a novel heterostructure electrocatalyst composed of cobalt-molybdenum (CoMo) alloy particles integrated with CoMoP nanosheets via the method of template-assisted conversion, followed by electrodeposition. Thanks to the strong interfacial coupling and synergistic effect between CoMo alloy particles and CoMoP nanosheets, the prepared CoMo/CoMoP/NF shows outstanding activity with overpotentials of only 29 mV for the hydrogen evolution reaction (HER) and 246 mV for the oxygen evolution reaction (OER) in 1 M KOH at a current density of 10 mA cm-2. Furthermore, the assembled CoMo/CoMoP || CoMo/CoMoP electrode can attain 10 mA cm-2 with a low battery voltage of 1.54 V. This study offers a valuable reference to the construction of bimetallic alloy/bimetallic phosphide heterostructure electrocatalysts, which applies to the large-scale application of electrocatalytic energy conversion technology.

Metal-Organic Framework-Derived Three-Dimensional Macropore Nitrogen-Doped Carbon Frameworks Decorated with Ultrafine Ru-Based Nanoparticles for Overall Water Splitting.

Hydrogen energy with the advantages of green, sustainability, and high energy density has been considered as an alternative to fossil fuel energy. Water electrolysis to produce hydrogen is a promising energy conversion technology but limited to the large overpotential; thus, a highly efficient electrocatalyst is urgently needed. Herein, Ru-based electrocatalysts including an ultrathin Ru/three-dimensional (3D) macropore N-doped carbon framework (Ru/3DMNC) and ultrathin RuO2/3D macropore N-doped carbon framework (RuO2/3DMNC) are first prepared using a Zn-centered metal-organic framework (MOF, ZIF-8) as the precursor. The ultrathin 3D macropore framework structure together with N doping endows the as-synthesized Ru-based electrocatalysts with abundant exposed catalytic active sites, good electroconductivity, and excellent electron/mass transport, accomplishing improved activities for hydrogen evolution reaction (HER), oxygen evolution reaction (OER), and overall water splitting. The Ru/3DMNC and RuO2/3DMNC present low overpotentials of 50.96 and 216.74 mV to reach a current density of 10 mA cm-2. Moreover, the overall water splitting device constructed by Ru/3DMNC and RuO2/3DMNC as the cathode and anode catalysts, respectively, affords a current density of 10 mA cm-2 only at 1.51 V, which is superior to the Pt/C||RuO2 cell (1.573 V). This work provides a rational strategy to design and construct the efficient framework structure electrocatalysts for water splitting using MOFs as the precursor.

Ni3B as p-Block Element-Modulated Cocatalyst for Efficient Photocatalytic CO2 Reduction.

Due to the multiple electron and proton transfer processes involved, the photogenerated charges are easily recombined during the photocatalytic reduction of CO2, making the generation of the eight-electron product CH4 kinetically more difficult. Herein, Ni3B nanoparticles modulated by p-block element were combined with TiO2 nanosheets to construct a novel Schottky junction photocatalyst (Ni3B/TiO2) for the selective photocatalytic conversion of CO2 to CH4. The formed Ni3B/TiO2 photocatalyst with Schottky junction ensures a transfer pathway of photogenerated electrons from TiO2 to Ni3B, which facilitates the accumulation of electrons on the surface of Ni3B and subsequently improves the activity of photocatalytic CO2 reduction to CH4. The optimized Ni3B/TiO2 Schottky junction shows an improved CH4 yield of 30.03 µmol g-1 h-1, which was much higher than those of TiO2 (1.62 µmol g-1 h-1), NiO/TiO2 (2.44 µmol g-1 h-1), and Ni/TiO2 (4.3 µmol g-1 h-1). This work demonstrated that the introduction of p-block elements can alleviate the scaling relationship effect of pure metal cocatalysts to a certain extent, and the modified Ni3B can be used as a promising new cocatalyst to effectively improve the selective photocatalytic of CO2 to CH4.

Synergizing Cobalt Ruthenium Alloy with Chromium Oxyhydroxide for Highly Efficient Electrocatalytic Water Splitting.

Constructing a coupling interface of multicomponents with different functions is of considerable importance for designing an advanced bifunctional water splitting electrode. Particularly, designing and developing alloy/oxyhydroxide-integrated electrodes have emerged as a tendency yet remain a considerable challenge. In this work, a novel 3D nanostructure electrocatalyst assembled from CoRu nanoalloy and CrOOH nanosheets (denoted as CoRu-CrOOH/NF) was directly grown on nickel foam via a successive hydrothermal method. The unique synergy in CoRu-CrOOH/NF heterostructures is not only conducive to strengthening charge transfer capability and accelerating the reaction kinetics but also favors the redistribution of charge within the interface, thus improving the electrocatalytic performance. In view of the above-mentioned points, the resultant CoRu-CrOOH/NF displays outstanding catalytic performance with overpotentials of 26 and 272 mV at 10 mA cm-2 for hydrogen evolution reaction (HER) and 50 mA cm-2 for oxygen evolution reaction (OER). Remarkably, the symmetrical two-electrode cell using CoRu-CrOOH/NF only acquires 1.47 V at 10 mA cm-2 in 1.0 M KOH, which is superior to many other state-of-the-art overall water-splitting electrocatalysts. This holistic work provides a new insight to designing alloy/oxyhydroxide-integrated electrodes for high-efficiency overall water splitting.

Synergistically Integrating Nickel Porous Nanosheets with 5d Transition Metal Oxides Enabling Efficient Electrocatalytic Overall Water Splitting.

An integration hydrogen adsorption benign component such as a metal with an oxygen-containing reactant adsorption benign component such as metal oxide allows for efficient overall water splitting in alkaline solutions and yet remains a considerable challenge. Herein, 5d transition metal oxide WO2 and WO3 (denoted as WOx) nanoparticles are purposely integrated with a porous Ni nanosheet array grown on nickel foam (NF) to design a strongly coupled Ni/WOx/NF porous nanosheet array electrocatalyst. Through the anion exchange of Ni(OH)2 nanosheets with tungstate, followed by hydrogenation treatment, abundant Ni/WOx interfaces with strong coupling interaction are generated. Benefiting from the strong synergies between Ni and WOx and the unique nanostructure, Ni/WOx/NF only requires the overpotentials of 42 mV for hydrogen evolution reaction (HER) and 395.7 mV for oxygen evolution reaction (OER) to achieve the current densities of 10 and 100 mA cm-2, respectively. Furthermore, the Ni/WOx/NF can achieve a current density of 10 mA cm-2 at a low cell voltage of 1.54 V in a two-electrode system. This work opens a novel avenue for the design of high-performance but low-cost electrocatalysts for overall water splitting.

Interfacial engineering of CeO2 on NiCoP nanoarrays for efficient electrocatalytic oxygen evolution.

Transition metal phosphides (TMP)-based oxygen evolution reaction (OER) catalysts constructed by interface engineering strategy have a broad prospect due to their low cost and good performance. Herein, a novel CeO2/NiCoP nanoarray with intimate phosphide (NiCoP)-oxide (CeO2) interface was developed via in situ generation on nickel foam (NF). This structure is conducive to increasing active sites and accelerating charge transfer, and may be conducive to regulating electronic structure and adsorption energy. As expected, optimal 1.4-CeO2/NiCoP/NF delivers a low overpotential of 249 mV at the current density of 10 mA cm-2 with a Tafel slope of 77.2 mV dec-1. CeO2/NiCoP/NF boasts one of the best OER catalytic materials among recently reported phosphides (TMP)-based OER catalysts and composite catalysts involving CeO2. This work provides an effective strategy for the construction of hetero-structure with CeO2 with oxygen vacancies to improve the OER performance of phosphides.

Iron and chromium co-doped cobalt phosphide porous nanosheets as robust bifunctional electrocatalyst for efficient water splitting.

It is still a huge challenge to develop highly efficient and low-cost non-precious metal-based electrocatalysts for overall water splitting in alkaline electrolytes. Herein, Cr and Fe co-doped CoP porous mesh nanosheets (Mesh-CrFe-CoP NSs) were synthesized through hydrolysis reaction, ion exchange etching and subsequent low-temperature phosphating process. The Mesh-CrFe-CoP NSs provides overpotentials at a current density of 10 mA cm-2under alkaline electrolyte of 103.7 mV and 256.4 mV for HER and OER, respectively. Furthermore, when using Mesh-CrFe-CoP NSs as anode and cathode, the water splitting system could afford a current density of 10 mA cm-2at 1.55 V, which is better than an electrolytic cell composed of 20% Pt/C and RuO2. The excellent electrocatalytic performance of Mesh-CrFe-CoP NSs is attributed to the co-doping and porous nanostructure. Specifically, the Cr and Fe co-doped porous CoP nanosheets electrocatalyst not only provided abundant exposure active sites, accelerated the entry of liquid and the diffusion of gas, but also regulated the electronic environment of active sites, and thus enhanced the electrochemical performance. This work proposes a strategy for the rational design of highly efficient and stable non-precious metal co-doped phosphide electrocatalysts in the of electrochemical water splitting.

Stable and enhanced electrochemical performance based on hierarchical core-shell structure of CoMn2O4@Ni3S2electrode for hybrid supercapacitor.

Herein, accessible and low-cost CoMn2O4@Ni3S2core-shell nanoneedle arrays have been prepared via a two-step approach comprised with hydrothermal-calcination and electrochemical deposition procedures, successfully. In the beginning, CoMn2O4nanoneedle arrays took root on Ni foam to form the core skeleton and subsequently, hierarchical Ni3S2nanosheets uniformly overlaid on the surface of CoMn2O4nanoneedles shaping the shell structure. This CoMn2O4@Ni3S2material was measured directly as supercapacitor electrode and presented high specific capacity of 192.2 mAh g-1with current density of 1 A g-1. Besides, the electrode delivered outstanding cyclical stability as the capacity retention attained 90.2% after charge-discharge measurement at a large current density of 10 A g-1for 10 000 cycles. Furthermore, a hybrid supercapacitor assembled by CoMn2O4@Ni3S2cathode and activated carbon anode represented a high energy density of 51.2 Wh kg-1with the power density of 1030.0 W kg-1. This work shows a facile and inexpensive procedure to design high-performance and strong-stability supercapacitor electrodes.

Noble-metal-free Co x P nanoparticles: modified perovskite oxide ultrathin nanosheet photocatalysts with significantly enhanced photocatalytic hydrogen evolution activity.

The integration of semiconductor-based photocatalysts with noble-metal-free cocatalysts has great significance for practical applications. In this work, for the first time, novel Co x P/K+Ca2Nb3O10 - nanostructures (abbreviated as Co x P/KCNOus) were synthesized by integrating noble-metal-free Co x P nanoparticles onto the surface of K+Ca2Nb3O10 - ultrathin nanosheets (abbreviated as KCNOus), and exhibited enhanced photocatalytic hydrogen generation. Under the irradiation of xenon light, the hydrogen generation rate of the resulting optimal Co x P/KCNOus reached up to 90.4 µmol g-1 h-1, approximately 5.78 times higher than that of single-component KCNOus. The apparent quantum efficiency (AQE) of Co x P/KCNOus is 1.32% at 350 nm. Based on photoluminescence (PL), UV-vis diffuse reflectance spectroscopy (UV-vis DRS), and photo-electrochemical analyses, possible reasons for this improved photocatalytic activity can be ascribed to the enhanced light absorption capacity and strong separation efficiency of photoinduced carriers over Co x P/KCNOus owing to the formation of the interfaces between KCNOus and Co x P nanoparticles. It is believed that this work will provide a new insight into the development ofefficient and low-cost noble-metal-free cocatalysts for photocatalytic hydrogen evolution reactions.

Hierarchical CoO@Ni(OH)2 core-shell heterostructure arrays for advanced asymmetric supercapacitors.

Constructing multicomponent electrode materials with a rational structure is an effective route to develop high-performance supercapacitors. We herein report a novel nickel-foam-supported hierarchical CoO@Ni(OH)2 nanowire-nanosheet core-shell heterostructure array synthesized by a facile hydrothermal-electrodeposition strategy. The core CoO nanowire arrays with good electrical conductivity and shell Ni(OH)2 nanosheets with thickness of ∼ 2 nm synergistically contributes to increased active sites, fast mass transfer, and improved structural stability. Consequently, the optimal CoO@Ni(OH)2-400 s architecture delivers a high specific capacitance of 1418.2 F g-1 at 1 A g-1 and 93.7% retention after 5000 cycles. Furthermore, the CoO@Ni(OH)2//activated carbon asymmetric supercapacitor could achieve an outstanding energy density of up to 92.47 W h kg-1 at 800 W kg-1. This simple but effective strategy provides insight into the development of core-shell hierarchical architectures for constructing high-performance supercapacitors.

Nanowire-assembled Co3O4@NiS core-shell hierarchical with enhanced electrochemical performance for asymmetric supercapacitors.

In this study, a three-dimensional (3D) hierarchical Co3O4@NiS core-shell heterostructure supported on nickel foam (NF) has been constructed. This Co3O4@NiS/NF can directly serve as a binder-free electrode for a pseudocapacitor, which could achieve a high specific capacitance of 1395.3 F g-1 at a current density of 1 A g-1 in 6 M KOH electrolyte, and an ideal rate capability of 711 F g-1 at a current density of 10 A g-1. Additionally, the electrode has a high capacitance retention of 89.9% after 5000 cycles. The asymmetric supercapacitor exhibits the maximum energy density of 61.34 W h kg-1 at a power density of 800 W kg-1, as well as an excellent cycling life of 89.3% capacitance retention. The enhanced electrochemical performance can be mainly ascribed to the special 3D core-shell nanowire arrays nanostructure with great conductivity, enlarged surface area, abundant accessible active sites and intrinsic stability. We anticipate that the present Co3O4@NiS/NF could be a promising electrode material for energy storage applications.

In situ synthesis of silver supported nanoporous iron oxide microbox hybrids from metal-organic frameworks and their catalytic application in p-nitrophenol reduction.

Ag nanoparticles (NPs) are successfully grown in situ on nanoporous Fe2O3 microboxes (Ag/Fe2O3) simply by annealing Prussian blue (PB) in the presence of silver nitrate for the first time. The catalytic activity of the Ag/Fe2O3 microboxes for the reduction of p-nitrophenol (PNP) with NaBH4 is measured by UV-vis spectroscopy. It is found that the composites exhibit bifunctional properties with high magnetization and excellent catalytic activity toward PNP reduction. The high catalytic activity of the catalyst might be attributed to its high surface area and the synergistic effect on the delivery of electrons between Ag NPs and Fe2O3 microboxes. In addition, efficient reduction is observed and found to depend upon the content of Ag in the Ag/Fe2O3 microboxes. The dosage of the catalyst and the reaction temperature were investigated. Furthermore, the catalysts can be easily recycled by applying an external magnetic field while maintaining the catalytic activity without significant decrease even after running six times. The unique properties provide an ideal platform to study various metal/Fe2O3 catalysts which can be potentially applied in a wide variety of fields of catalysis and green chemistry.

Nitrogen- and fluorine-doped bimetallic carbide as active and stable oxygen reduction reaction electrocatalyst.

Nitrogen- and fluorine-doped bimetallic carbide composites with graphite matrix (abbreviated as C19Cr7Mo24/NG and C19Cr7Mo24/FG) are synthesized through carbonization at 1300 °C. The C19Cr7Mo24/NG displays an initial half-wave potential (E1/2) of 0.873 V and suffers merely 3 mV decrease in E1/2 within 60,000 CV cycles for oxygen reduction reaction (ORR) in alkaline media. A H2/O2 fuel cell testing system using the C19Cr7Mo24/NG as cathode maintains 95.9% of the initial peak power density (1.08 W cm-2) within 60,000 cycles. The C19Cr7Mo24/FG shows higher ORR activity than the C19Cr7Mo24/NG. The positive and negative charge centers caused by the N or F dopants are the critical reasons to their high activities. While F and bimetallic carbide more favor electron transfer respectively than the N and monometallic carbide. Their excellent stabilities originate from interactions among atoms due to electron transfer and the intrinsic chemical inertness of graphite and bimetallic carbides.

Integrating bimetallic borides with g-C3N4 containing cyanamide defects for efficient photocatalytic nitrogen fixation.

The sustainable generation of ammonia by photocatalytic nitrogen fixation under mild conditions is fascinating compared to conventional industrial processes. Nevertheless, owing to the low charge transfer efficiency, the insufficient light absorption capacity and limited active sites of the photocatalyst cause the difficult adsorption and activation of N2 molecules, thereby resulting in a low photocatalytic conversion efficiency. Herein, a novel bimetallic CoMoB nanosheets (CoMoB) co-catalyst modified carbon nitride with dual moiety defects (CN-TH3/3) Schottky junction photocatalyst is designed for photocatalytic nitrogen reduction reaction (NRR). The photocatalytic nitrogen reduction rate of the optimized CoMoB/CN-TH3/3 photocatalyst is 4.81 mM·g-1·h-1, which is 6.2 and 2.2 times higher than carbon nitride (CN) (0.78 mM·g-1·h-1) and CN-TH3/3 (2.21 mM·g-1·h-1), respectively. The excellent photocatalytic NRR performance is ascribed not only to the introduction of dual moiety defects (cyano and cyanamide groups) that extends the visible light absorption range and promotes exciton polarization dissociation, but also to the formation of interfacial electric field between CoMoB and CN-TH3/3, which effectively facilitates the interfacial charge transfer. Thus, the synergistic interaction between CN-TH3/3 and CoMoB further increases the electron numble of CoMoB active sites, which effectively strengthens the adsorption and activation of N2 and weakens the NN triple bond, thereby enhancing the photocatalytic NRR activity. This work highlights the introduced dual moiety defects and bimetallic CoMoB co-catalyst to synergistically enhance the photocatalytic nitrogen reduction performance.

Molybdenum diselenide/polymeric carbon nitride dual-homojunction photocatalyst with multi-step charge transfer for efficient catalytic carbon dioxide reduction.

Due to the high dissociation energy of carbon dioxide (CO2) and sluggish charge transfer dynamics, photocatalytic CO2 reduction with high performance remains a huge challenge. Herein, we report a novel dual-homojunction photocatalyst comprising of cyano/cyanamide groups co-modified carbon nitride (CN-TH) intramolecular homojunction and 1 T/2H-MoSe2 homojunction (denoted as 1 T/2H-MoSe2/CN-TH) for enhanced photocatalytic CO2 reduction. In this dual-homojunction photocatalyst, the intramolecular CN-TH homojunction could promote the intralayer charge separation and transfer owing to the strong electron-withdrawing capabilities of the two-type cyanamide, while the 1 T/2H-MoSe2 homojunction mainly contributes to a promote interlayer charge transport of CN-TH. This could consequently induce a tandem multi-step charge transfer and accelerate the charge transfer dynamics, resulting in enhanced CO2 reduction activities. Thanks to this tandem multi-step charge transfer, the optimized 1 T/2H-MoSe2/CN-TH dual-homojunction photocatalyst presented a high CO yield of 27.36 µmol·g-1·h-1, which is 3.58 and 2.87 times higher than those of 1 T/2H-MoSe2/CN and 2H-MoSe2/CN-TH single homojunctions, respectively. This work provides a novel strategy for efficient CO2 reduction via achieving a tandem multi-step charge transfer through designing dual-homojunction photocatalyst.

Negative differential resistance in MX- and MMX-type iodide-bridged platinum complexes.

Negative differential resistance (NDR) was discovered in MX- and MMX-type iodide-bridged platinum complexes for the first time. The low resistance of the complex observed under the large current cannot be explained only by the Joule heat. The intrinsic charge-ordering states are considered to play an important role in the NDR of these compounds.

Mechanical and friction properties of agricultural plastic film during autumn harvest period of cotton in Xinjiang, China.

Agricultural plastic films have caused serious plastic pollution. There are many studies that consider mechanical recycling an appropriate system for the recovery of post-consumption agricultural mulch film. The recovery effect of plastic film depends on the mechanical properties, the level of dirtiness of the post-consumption film, and the recycling process itself. In this study, the mechanical properties of four types of polyethylene plastic films with a thickness of 8, 10, 12, and 10 µm, weather-resistant, commonly used in Xinjiang cotton fields, were tested. As well as the friction coefficient between the film and soil, the cotton stalk, boll shell, and leaf with different moisture contents were measured. Then, the self-propelled straw chopping and residual film recycling combined machine collected the four types of mulch films. The results showed that the longitudinal mechanical properties of the plastic film were greater than the transversal ones, with the exception of the nominal tensile strain at break, and the tensile characteristics of the mulching film covered with soil were greater than those without soil. The dynamic or static friction coefficient between the film and the contact material had a linear relationship with the moisture content of the material. During the recycling operation, the better the mechanical properties of the plastic film, the higher the pick-up rate of the mulch film. The maximum longitudinal tensile force of 12-µm plastic film was 3.42 N, and the nominal tensile strain at break was 303.09%. The pick-up rate reached more than 93% when the 12-µm plastic film was recovered in autumn, which effectively reduced the residue of plastic film coverage in the current year. Moreover, the more soil that was present on the much film, the greater the soil content of the recycled film roll, and the stalk content also increased, but the change was small. The research provides a reference for the mechanical and the friction features of agricultural plastic film in Xinjiang, and provides a theoretical basis for the formulation of standards for film thickness and mechanical properties, as well as the design and optimization of a residual film collecting machine in the cotton field.

Zinc and fluorine ions dual-modulated NiCoP nanoprism array electrocatalysts for efficient water splitting.

Designing efficient, stable, and low-cost bifunctional catalysts for overall water splitting is significant but challenging. In this work, Zn and F ions co-doped NiCoP nanoprism arrays grown directly on nickel foam (Zn/F-NiCoP/NF) was synthesized via hydrothermal method followed by phosphorization treatment. The resultant Zn/F-NiCoP/NF exhibits high electrocatalytic activity towards hydrogen evolution reaction (HER, η10 = 59 mV) and oxygen evolution reaction (OER, η50 = 285 mV). An alkaline electrolyzer using Zn/F-NiCoP/NF as both cathode and anode requires a low cell voltage of 1.568 V at a current density of 10 mA cm-2 with a high long-term stability of up to 40 h, which outperforms many reported Ni,Co-based catalysts. Density functional theory (DFT) calculations proof that simultaneous doping of NiCoP with Zn and F ions provides flexibility to regulate the electronic configuration and downshifts the transition metal d-band center, thereby optimizing adsorption energy between reactants and intermediates, which enhances the HER and OER catalytic activities. This work highlights that cation-anion co-doping strategy is an effective way to develop highly active transition metal phosphides electrocatalyst for water splitting.