Performance For Water Splitting Research Articles

La implanted band engineering of ZnO nanorods for enhanced photoelectrochemical water splitting performance

In the quest to improve photoelectrochemical water-splitting performance, we have doped lanthanum (La) in highly crystalline zinc oxide (ZnO) nanorods (NRs) using a facile and low-temperature hydrothermal route and successful substitution of La3+ at the Zn2+ site is confirmed from structural and chemical analysis. The tapered NRs morphology gained after La doping resulted in lower optical bandgap of 3.17 eV, enhanced visible light trapping, and multiphoton absorption, which assist in achieving good PEC activity. The La doping also offered higher Urbach energy (EU), subsidizing the number of oxygen vacancies. The UPS spectra show that La doping reduces conduction band energy level and endorses smooth charge transportation. The La-doped ZnO exhibits two times enhancement in photocurrent (1.54 mA·cm−2) compared to pristine ZnO (0.81 mA·cm−2). The higher applied bias to the photon conversion efficiency of ∼1.14% for La-doped ZnO confirms the efficient utilization of solar energy. The EIS measurements demonstrated reduction in charge transfer resistance with La-doping. Mott-Schottky analysis shows that La doping lowers the flat-band potential and enhances charge transportation, making it a potential photoanode for PEC water-splitting applications.

In-Sb Covalent Bonds over Sb2Se3/In2Se3 Heterojunction for Enhanced Photoelectrochemical Water Splitting.

Antimony selenide is a promising P-type photocatalyst, but it has a large number of deep energy level defects, leading to severe carrier recombination. The construction of a heterojunction is a common way to resolve this problem. However, the conventional heterojunction system inevitably introduces interface defects. Herein, we employ in situ synthesis to epitaxially grow In2Se3 nanosheets on Sb2Se3 nanorods and form In-Sb covalent interfacial bonds. This petal-shaped heterostructure reduced interface defects and enhanced the efficiency of carrier separation and transport. In this work, the photocurrent density in the proposed Sb2Se3/In2Se3 photocathode is 0.485 mA cm-2 at 0 VRHE, which is 30 times higher than that of pristine Sb2Se3 and it has prominent long-term stability for 24 h without obvious decay. The results reveal that the synergy of the bidirectional built-in electric field constructed between In2Se3 and Sb2Se3 and the solid In-Sb interfacial bonds together build a high-efficiency transport channel for the photogenerated carriers that display enhanced photoelectrochemical (PEC) water-splitting performance. This work provides efficient guidance for reducing interface defects via the in situ synthesis and construction of interfacial bonds.

Effects of La-N Co-Doping of BaTiO3 on Its Electron-Optical Properties for Photocatalysis: A DFT Study.

In cation-anion co-doping, rare earth elements excel at regulating the electronic structure of perovskites, leading to their improved photocatalytic performance. In this regard, the impact of co-doping rare earth elements at the Ba and Ti sites in BaTiO3 on its electronic and photocatalytic properties was thoroughly investigated based on 2 × 2 × 2 supercell structures of BaTiO3 with different La concentrations of 12.5% and 25% using DFT calculations. The band structure, density of states, charge density difference, optical properties, and the redox band edge of the co-doped models mentioned above were analyzed. The results indicated that the BaTiO3 structure co-doped with 25% La at the Ti site exhibited higher absorption in the visible range and displayed a remarkable photocatalytic water-splitting performance. The introduced La dopant at the Ti site effectively reduced the energy required for electronic transitions by introducing intermediate energy levels within the bandgap. Our calculations and findings of this study provide theoretical support and reliable predictions for the exploration of BaTiO3 perovskites with superior photocatalytic performances.

Transition‐Metal‐Doped TiO2 Nanorods with High‐Visible‐Light Response via a Simple Hydrothermal Method

Transition‐metal‐ion doping is an effective method to shorten bandgap and enhance visible‐light absorption of TiO2, but there are still some serious challenges for most doping technologies, such as nonuniform doping, severe lattice damages, metal atoms agglomeration, and inactivated impurities. Herein, a simple and universal hydrothermal method is developed to realize the effective transition‐metal ions doping of TiO2 (including Fe, Co, Mn, Cu, V, and Cr). The photoelectrochemical water splitting performances of Cr‐doped TiO2 nanorods with multifarious Cr ion valence states (Cr3+ or Cr6+ ions), various Cr‐ion concentrations, with or without oxygen vacancy activation are emphatically and systematically studied. Experiments and theoretical calculations demonstrate that the remarkably enhanced carrier separation and injection efficiencies are the key factors to improve the visible‐light photoactivity, benefiting from the homogeneous distribution of impurity atoms and the incorporation of oxygen vacancies. The Cr3+‐ion‐doped TiO2 nanorod arrays with oxygen vacancy activation (Cr3+/Ov–TiO2) displays an impressive incident photon‐to‐electron conversion efficiency of 5.4% at 450 nm visible light, far superior to the pure TiO2 of 0.03%. Furthermore, no obvious photocurrent decay is observed in the Cr3+/Ov–TiO2 photoanode after 12 h continuous light illumination.

Boosting electrocatalytic hydrogen generation from water splitting with heterostructured MoS2/NiFe2O4 composite in alkaline media

Design and synthesis of earth-abundant and robust bifunctional electrocatalysts have been greatly sought for commercialization of the technology for clean and renewable energy and replacement of the energy equipment based on fossil fuels. In this work, a facile hydrothermal approach is used to synthesize MoS2/NiFe2O4-based nanocomposite as a novel electrocatalyst for alkaline water splitting. Surface analysis was conducted using scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Benefiting from the synergy of lamellar MoS2 and crystalline NiFe2O4, the obtained MoS2/NiFe2O4 composite shows excellent hydrogen evolution reaction (η10 = 190 mV, η50 = 279 mV) and oxygen evolution reaction (OER) (η50 = 350 mV, η100 = 360 mV) activity with high TOF (0.01 s−1@190 mV for HER and 0.24 s−1 @360 mV for OER) and displays good electrochemical stability. Explicitly, the electrocatalyst requires a cell voltage of 1.69 V to drive overall water splitting at a current density of 10 mA cm−2. Density functional theory (DFT) results demonstrated that the MoS2/NiFe2O4 composite electrocatalyst has smaller hydrogen adsorption free energy (|ΔGH*|) than pristine MoS2 and NiFe2O4, which demonstrates the effective adsorption and cleavage of water on the catalyst surface. This work thus presents an approach for the synthesis and rational design of metal oxide/metal sulfide hybrids as an electrocatalyst with high performance for overall water splitting.

Prussian blue analogue-derived Co-Ni5P4 porous nanosheet arrays composite coal-based carbon nanofibers as efficient self-supported electrocatalyst for overall water splitting

The development of economical, earth-rich, and high-performance transition metal phosphides electrocatalysts is crucial for water splitting. Herein, the NiCo PBA/Ni(OH)2 hierarchical nanostructure arrays are in situ grown on the coal-based carbon nanofibers (C-CNFs) using hydrothermal and co-precipitation methods. Subsequently, the Co-doped Ni5P4 porous nanosheet arrays composite coal-based carbon nanofibers electrocatalyst (Co-Ni5P4@C-CNFs) is obtained through low-temperature phosphorization process. Benefiting from cation-doped, porous nanosheet arrays structure and self-supported conductive substrates, the Co-Ni5P4@C-CNFs has excellent electrocatalytic performance for overall water splitting. It provides low overpotentials of 75 mV for hydrogen evolution reaction (HER) and 231 mV for oxygen evolution reaction (OER) to achieve the current density of 10 mA cm−2 in 1 M KOH electrolyte. Furthermore, the Co-Ni5P4@C-CNFs demonstrates a low overall water splitting cell voltage of 1.537 V at current density of 10 mA cm−2 and remarkable long-term stability for over 160 h. It outperforms the most transition metal phosphide bifunctional electrocatalysts reported to date. This research provides a novel strategy for synthesizing high-performance transition metal phosphides bifunctional electrocatalysts.

Ti3C2 mediates the NiFe-LDH layered electrocatalyst to enhance the OER performance for water splitting

Oxygen evolution reaction (OER) is a very complex process with slow reaction kinetics and high overpotential, which is the main limitation for the commercial application of water splitting. Thus, it is of necessary to design high-performance OER catalysts. NiFe based layered double hydroxides (NiFe-LDHs) have recently gained a lot of attention due to their high reaction activity and simple manufacturing process. In this study, a novel electrocatalyst based on NiFe-LDH was constructed by introducing Ti3C2, which was utilized to modulate the structural and electronic properties of the electrocatalysts. Structural examinations reveal that the Ti3C2 of 2D structure successfully dope the NiFe-LDHs nanosheets, forming NiFe-LDH/Ti3C2 heterojunctions. Firstly, the heterojunction substantially reduces the charge transfer resistance, promoting the electron migration between the LDH nanosheets. Secondly, theoretical calculations demonstrate that the energy barrier between the rate-determining step from *OH to *O is lowered, favoring the formation of the reaction intermediates and thus the occurrence of OER. As a result, the composite electrocatalyst exhibits a low overpotential of 334 mV at a current density of 10 mA/cm2 and a small Tafel slope of 55 mV/dec, which are superior to those of the NiFe-LDH by 11.2 % and 38.5 %, respectively. This study provides inspiration for promoting the performances of NiFe based electrocatalysts by utilizing 2D materials.

CoFe(OH)x-Co3O4/NF as highly efficient electrocatalyst for oxygen evolution and urea oxidation reactions at high current densities

The advancement of an affordable and highly effective catalyst for the oxygen evolution reaction (OER) is essential to enhance the performance of overall water splitting (OWS). Here, we report a highly efficient nickel foam (NF)-supported CoFe(OH)x-Co3O4/NF heterostructure catalyst for OER. The CoFe(OH)x-Co3O4/NF heterostructure catalyst contain amorphous phase CoFe(OH)x and crystalline Co3O4, and the synergistic interaction between the two different phases reduces the charge transfer resistance, accelerates the kinetic processes of electrocatalysis and makes the catalysts exhibit excellent catalytic performance. In 1.0 M KOH solution, an overpotential (η) of merely 262 mV is needed to attain a current density of 100 mA cm−2. Even at high current densities demanded for commercial applications, the overpotentials remain very low (η500 = 291 mV, η1000 = 319 mV). The catalytic activity of CoFe(OH)x-Co3O4/NF has exceeded that of most non-noble metal OER catalysts documented in the literature. Furthermore, the CoFe(OH)x-Co3O4/NF catalyst demonstrates superior catalytic stability to OER, with only a 23 mV potential increase after 24 h of stability testing at a high current density of 500 mA cm−2. Owing to the heterostructure, the CoFe(OH)x-Co3O4/NF catalyst also exhibits excellent catalytic performance for the urea oxidation reaction (UOR), and the use of UOR instead of OER at the anode of OWS significantly reduces the cell voltage, thereby reducing the electrolytic energy consumption. The findings in this work offer precious insights into the design of OWS anode catalysts and their important applications in industrial water electrolysis. These insights are crucial for advancing the development of highly efficient and sustainable water electrolysis processes, which is essential for the production of green hydrogen and other valuable chemicals.

Facile synthesis of TiO2 nanothorn-coated Cu2O nanowires with improved stability and performance for photoelectrochemical water splitting

Copper(I) oxide (Cu2O) based photocathodes are promising in photoelectrochemical (PEC) water splitting due to their bandgap, natural abundance, and low cost. However, the stability issues have impeded their practical application. This study presents a solution through a novel photocathode, TiO2 nanothorns-coated Cu2O nanowires (TCNW), synthesized using simple wet chemical methods. TCNW outperformed pristine Cu2O nanowires (CNW), achieving a stable PEC current density of ∼3.8 mA∙cm−2 at 0 V vs RHE, compared to ∼1.9 mA∙cm−2 of CNW. TCNW also displayed an H2 evolution rate of ∼64.2 μmol∙cm−2∙h−1 with a 93.9% faradaic efficiency, whilst CNW reached only ∼6.8 μmol∙cm−2∙h−1 and 37.3%. These improvements stem from the protective TiO2 nanothorn layer, which enhances light absorption (300–500 nm) and improves charge separation and transfer by forming a p-n junction with Cu2O. This work underscores the importance of well-crafted surface p-n junctions and conformal protective layers in optimizing the efficiency and stability.

Fabrication of 0D/2D CoFe2O4/CoFe LDH composite intruded within CNTs network as a high-performance electrocatalyst for oxygen evolution and hydrogen evolution reactions

Designing highly efficient and durable multicomponent heterostructured composites as catalytic materials for concomitant hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) is highly desirable. Researchers all over the world are continuously working to develop such materials. Herein, CNTs wrapped CoFe2O4/CoFe LDH (CoF/CoFe LDH@CNTs) ternary composite is synthesized by hydrothermal and ultra-sonication routes. Numerous methods, including X-ray diffraction (XRD), scanning electron microscopy (SEM), cyclic voltammetry (CV), electrical Mott-Schottky, and electrochemical impedance spectroscopy (EIS) are employed to study structure, morphology, flat band potential, and electrochemical properties of prepared samples. In terms of water splitting performance, CoF/CoFe LDH@CNTs composite showed predominant performance for both HER and OER activities, as compared to its analogs (CoF and CoF/CoFe LDH). Faster electron transfer is also exhibited by CoF/CoFe LDH@CNTs, as it possesses a lower Tafel slope. For OER, CoF/CoFe, LDH@CNTs require a small overpotential of 170 mV to reach a current density of 10 mA cm−2 in 1 M KOH, with a Tafel slope of 42 mV dec-1. Similarly, for HER an overpotential of 218 mV is required to drive 10 mA cm−2 with a small Tafel slope of 31 mV dec-1. Impedance studies show a small value of charge transfer resistance (Rct = 1.11 Ω) for CoF/CoFe, LDH@CNTs. Significant electrochemical performance for CoF/CoFe, LDH@CNTs for both half-reactions (OER and HER) is ascribed to the synergy among electrochemically active CoF and CoFe LDH, and a highly conductive network of CNTs. The present strategy improves the electrochemical performance of electrochemical systems relevant to energy applications.

Multi-walled carbon nanotubes with embedded nickel sulphide as an effective electrocatalyst for Bi-functional water splitting

Water-splitting presents a viable solution to expanding energy needs. To maximise water-splitting performance, transition metal sulphides, a very efficient electrocatalyst, have been extensively researched. It is unable to generate hydrogen (H2) and oxygen (O2) because to active sites and weak electrical conductivity. Some carbon-based materials offer superior dispersion capacities and bigger active sites for charge transfer to circumvent these restrictions. This work presents an efficient electrocatalyst combining carbon nanotubes (CNTs) and electrochemically active Nickel sulphides, Ni17S18 (NiS), synthesized by using a wet-chemical approach. The improved electrocatalytic performance of NiS@CNTs can be attributed to higher surface area and higher electrical conductivity of CNTs. Furthermore, linear-sweep voltammetry (LSV) and electrochemical impedance analysis (EIS) were also utilized for the electrochemical investigations. The addition of CNTs to NiS showed a over-potential of 330 mV at 40 mA cm−2, with a Tafel slope of 47 mV dec−1 for OER. Similarly, we have also investigated the HER activity of the as-prepared electrocatalysts at the same current density, having a over-potential of 280 mV with a Tafel slope of 102 mV dec−1.

In situ growth of highly wrinkled 3D volcano-like Fe3S4/Ni3S2/WO3/NiFe LDH/NF electrocatalyst for overall water splitting

The rational design of efficient, cost-effective, and durable electrocatalysts is crucial for the realization of hydrogen production through water splitting. The present study describes the synthesis of a novel three-dimensional (3D) volcano-like Fe3S4/Ni3S2/WO3/NiFe LDH/NF (Layered Double Hydroxides/Nickel Foam) electrocatalyst with a highly wrinkled structure through a two-step hydrothermal method. The as-synthesized electrocatalyst exhibits an exceptionally low overpotential of 77 mV for the hydrogen evolution reaction (HER) and 131 mV for the oxygen evolution reaction (OER) at a current density of 10 mA cm−2, owing to the unique morphology and strong electronic interactions between Fe3S4, Ni3S2 and WO3 heterostructures. The Fe3S4/Ni3S2/WO3/NiFe LDH/NF electrocatalyst demonstrates exceptional performance in overall water splitting when employed as both anode and cathode, achieving a current density of 10 mA cm−2 at an impressively low cell voltage of 1.5 V as well as exhibiting remarkable durability with little degradation over a period of 12 hours. This study presents a straightforward approach for the synthesis of highly efficient and durable non-noble metal catalysts for overall water splitting under hydrothermal conditions.

Gamma-irradiated stibnite thin films set a remarkable benchmark performance for photoelectrochemical water splitting.

The study sets out to show the positive impact of sulfur vacancy engineering on the structural, morphological, optical, electrical, and photoelectrochemical (PEC) properties of Sb2S3 films synthesized using the spin coating technique. The produced films were exposed to γ-irradiation with different doses from 0 to 20 kGy. We have demonstrated the formation of sulfur vacancies and loss of oxygen content in the irradiated samples. XRD measurements revealed that all films exhibit a polycrystalline structure, and the crystallite size increases with the rising radiation dose, reaching the highest value of 87.4 nm measured for the Sb2S3 film irradiated with 15 kGy. The surface roughness of the irradiated samples increases with increasing γ-irradiation dose. The increase in surface roughness not only raises the active sites but enhances the conductivity of the Sb2S3 material as well. The wettability properties of the irradiated films were affected by γ-irradiation doses and the sample irradiated with 15 kGy exhibited the lowest hydrophobicity compared to others. The Hall measurements reveal that irradiated samples exhibit p-type semiconductor behavior. The optical band gap decreased progressively from 1.78 eV to 1.60 eV up to the irradiation dose of 15 kGy and slightly increased thereafter. The irradiated sample with 15 kGy showed a maximum photocurrent density of ca. 1.62 mA cm-2 at 0 V vs. reverse hydrogen electrode (RHE) under AM 1.5 G illumination with applied bias photon-to-current efficiency (ABPE) of 0.82% at 0.47 V vs. RHE, suggesting superior PEC water splitting performance compared to other samples. At 0 V vs. RHE and 648 nm, the incident photon current efficiency (IPCE) and absorbed photon current efficiency (APCE) of the photocathode irradiated with 15 kGy are significantly higher than those of the other photocathodes with values of 9.35% and 14.47%, respectively. Finally, Mott-Schottky measurement was also performed on all photocathodes to estimate their acceptor density and flat band potential.

Construction of 2D/2D BCNS/Ti3C2 heterojunction with boron-doped g-C3N4 and Ti3C2 MXene for enhanced photocatalytic water splitting

Graphitic carbon nitride (g-C3N4) has attracted great interest in photocatalytic water splitting. However, the poor photogenerated charge carriers transfer and the insufficient driving force for oxygen evolution reaction limit its practical application. In this work, boron-doped g-C3N4 nanosheets (BCNS) have been synthesized by calcining a mixture of g-C3N4 and NaBH4. The synthesized BCNS were then combined with Ti3C2 MXene using electrostatic self-assembly to construct a 2D/2D BCNS/Ti3C2 heterojunction. The resultant BCNS retained the original framework of g-C3N4, while the optimized band structure of BCNS induced prominently enhanced visible light absorption, accelerated charge carriers separation, and the increased driving force for water oxidation compared to pure g-C3N4. Density functional theory further proved that BCNS can enhance the driving force for photocatalytic O2 evolution. Moreover, the construction of 2D/2D face-to-face BCNS/Ti3C2 heterojunction was carried out to further enhance photocatalytic performance due to the intimate contact interface and the accelerated separation and transfer of photogenerated charge carriers. As a result, the 2D/2D BCNS/Ti3C2 hetrojunction exhibited a dramatically improved photocatalytic water-splitting performance compared to pristine g-C3N4. This integrated engineering strategy, involving non-metal element doping and 2D/2D heterojunction construction, might provide a unique paradigm for the rational design of efficient photocatalysts for photocatalytic water splitting.

Metal single atom-oxygen modification induced transformation of carbon nitride-based heterojunctions from type-II to S-scheme for efficient photocatalytic overall water splitting

Constructing semiconductor S-scheme hetero-(homo-)junctions (SSHs) is one of the most effective ways to enhance the photocatalytic overall water splitting (POWS) performance, but encumbered by deficiency of efficient water-oxidizing semiconductors. Herein, tungsten single atom-oxygen group (W-O) modified polymeric carbon nitride (WPCN, an example of metal single atom-oxygen group modified PCN) was used as a water-oxidizing semiconductor to construct a CdS/WPCN SSH, for which the W-O modification plays a key role that causes transformation from a PCN/CdS type-II heterojunction to the CdS/WPCN SSH which exhibits remarkably enhanced photoexcited charge separation than single CdS and WPCN. Pt-CdS/WPCN exhibits 2.6 and 7.2 times higher POWS activity than Pt-WPCN and Pt-CdS, respectively, further demonstrating the key role of the SSH, and lower activity than Pt@Cr2O3-CdS/WPCN that exhibits 5.4-fold higher activity than Pt@Cr2O3-PCN/CdS, and especially, higher photochemical stability by suppressing rapid photocorrosion of CdS. The solar-to-hydrogen conversion efficiency of Pt@Cr2O3-CdS/ WPCN reaches 0.014 %, with an external quantum yield of 0.093 % at 420 nm. This work reveals the role of metal single atom-oxygen modification of PCN in SSHs and provides a way to suppress rapid photocorrosion of CdS.

Ti-mesh bipolar plate design and optimization for enhanced PEM electrolyzer performance in water splitting

Proton exchange membrane (PEM) electrolyzers are promising devices for hydrogen production from water splitting, but their performance and stability are still limited by various factors. This paper studies the effects of different structures on the performance of PEM electrolyzers, focusing on the working temperature, water conductivity, and the structure of bipolar plate. The results show that higher temperature and lower water conductivity enhance the electrolyzer performance, by increasing the catalyst activity and the proton transport. Moreover, a novel structure using a platinum-coated titanium mesh-based bipolar plate is proposed and tested. This structure improves the performance of the electrolyzer, by optimizing the mass transport, pressure drop, and water management in the electrolyzer. A 23-cell electrolyzer with this structure is developed and demonstrated. The electrolyzer achieves a high performance and stability, with a cell voltage of 1.742 V, a voltage efficiency of 85.0%, and a hydrogen production rate of 1.14 Nm3/h at 0.99 A/cm2. The observed cell voltage for the PEM electrolyzer is consistent with the documented range, typically spanning from 1.55 to 1.90 V at a current density of 0.99 A/cm2. This suggests that our bipolar plate design simplifies PEM electrolyzer manufacture while maintaining comparable performance to existing electrolyzers.

Interface engineering of hierarchical flower-like N, P, O-doped NixPy self-supported electrodes for highly efficient water-to-hydrogen fuel/oxygen conversion

Rational construction of efficient bifunctional catalysts with robust catalytic activity and durability is significant for overall water splitting (conversion between water and hydrogen fuel/oxygen) using non-precious metal systems. In this work, the hierarchically porous N, P, O-doped transition metal phosphate in the Ni foam (NF) electrode (hollow flower-like NPO/NixPy@NF) was prepared through facile hydrothermal method coupled with phosphorization treatment. The hierarchical hollow flower-like NPO/NixPy@NF electrodes exhibited high bifunctional activity and stability for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) in alkaline solutions. The optimized electrode showed low overpotentials of 76 and 240 mV for HER and OER to reach a current density of 10 mA cm−2, respectively. Notably, the NPO/NixPy@NF electrode only required a low voltage of 1.99 V to reach the current densities of 100 mA cm−2 with long-term stability for overall water splitting using the NPO/NixPy@NF|| NPO/NixPy@NF cell, surpassing that of the Pt/C-RuO2 (2.24 V@ 100 mA cm−2). The good catalytic and battery performance should be attributed to i) the open hierarchical structure that enhanced the mass transfer; ii) a highly conductive substrate that accelerated the electron transfer; iii) the rich heterojunction and strong synergy between Ni2P and Ni5P4 that improved the catalytic kinetic; iv) the proper-thickness amorphous phosphorus oxide nitride (PON) shell that realized the stability. This work demonstrates a promising methodology for designing bifunctional transition metal phosphides with high performance for efficient water splitting.

Layered double hydroxides derived prussian blue analogue nanocage confining NiCoP nanoparticles as efficient bifunctional electrocatalyst

Designing novel electrocatalysts with excellent catalytic activity for efficient water splitting is necessary to achieve the large-scale H2/O2 production from renewable resources. In this study, a facile hydrothermal method followed by low-temperature phosphorylation treatment was employed to fabricate a nanocage of prussian blue analogue encapsulating NiCoP nanoparticles (NiCoP@PBA), which was derived from the layered double hydroxide precursor. As a bifunctional non-precious metal electrocatalyst, NiCoP@PBA demonstrates superior performance in KOH electrolyte water splitting, with overpotentials of 59 mV for electrocatalytic hydrogen evolution reaction (HER) and 263 mV for oxygen evolution reaction (OER) at 10 mA cm−2. The catalyst also exhibits low Tafel slopes of 54 mV dec−1 for HER and 120 mV dec−1 for OER, reflecting efficient charge transfer kinetics. DFT simulations show that the Co–N moieties at the heterogeneous interface of NiCoP@PBA can optimize the surface electron distribution and energy states, thus facilitating efficient electron-hole pair separation, significantly enhancing catalytic activity for both HER and OER process, and significantly extending the electrocatalyst's service life. Our approach can be extended to more non-precious metal electrocatalysts, which is significant for the design of efficient bifunctional water splitting electrocatalysts.

Superiority of CuSe as a non-nobel electrocatalyst among copper chalcogens for overall water splitting reactions

Among the transition metals copper is one of the cheapest earth- abandoned elements which can enhance electrocatalytic activity. The Cu-based catalysts are superior for catalytic performance and stability in alkaline media for oxygen evolution reaction (OER) and exhibit high activity in acidic media for hydrogen evolution reaction (HER).Synthesized CuSe nanoparticle is found as the most efficient bifunctional electrocatalyst among the synthesized Cu chalcogenides for water splitting reaction. Electrocatalytic performance for water oxidation was investigated in alkaline solution1(M) KOH for OER and 0.5 (M) H2SO4 for HER. To achieve 10 mA/cm2, it was observed an over potential (mV) of 343 for OER and 126 for HER, which are much smaller than these of CuS (385,320) and CuO (410, 345) studied. In this article, we have elucidated some essential criteria need to be specified to evaluate the water splitting performance including onset potential, overpotential, Tafel slope, turnover frequency (TOF), and stability of the copper chalcogenide nanoparticles.

Ammonia-assisted Ni particle preferential deposition in Ni-Fe pyrophosphates on iron foam to improve the catalytic performance for overall water splitting

Designing efficient and cost-effective electrocatalysts for overall water splitting remains a major challenge in hydrogen production. Herein, ammonia was introduced to pyrophosphate chelating solution assisted Ni particles preferential plating on porous Fe substrate to form coral-like Ni/NiFe-Pyro electrode. The pyrophosphate with multiple complex sites can couple with nickel and iron ions to form an integrated network structure, which also consists of metallic nickel due to the introduction of ammonia. The large network structure in Ni/NiFe-Pyro significantly enhances the synergistic effect between nickel and iron and then improves the electrocatalytic performance. As a result, the coral-like Ni/NiFe-Pyro@IF exhibits good electrocatalytic activity and stability for oxygen evolution reaction (OER) and hydrogen evolution reaction (HER). The electrolyzer assembled with Ni/NiFe-Pyro@IF as cathode and anode just needs a low water-splitting voltage of 1.54 V to obtain the current density of 10 mA cm−2. Meanwhile, the stability test of Ni/NiFe-Pyro@IF is performed at the current densities ranging from 10 to 400 mA cm−2 for 50 h without any significant decay, indicating robust catalytic stability for overall water splitting. This strategy for synthesizing metal/metal pyrophosphate composites may provide a new avenue for future studies of efficient bifunctional electrocatalysts.