Electrocatalytic Hydrogen Evolution Research Articles

Research on the synthesis of transitional metal and post-transitional metal doping eolitic imidazolate framework-based electrocatalysts and electrocatalytic hydrogen evolution reaction

Research on the synthesis of transitional metal and post-transitional metal doping eolitic imidazolate framework-based electrocatalysts and electrocatalytic hydrogen evolution reaction

Defect engineering via gamma irradiation in scalable mechanical exfoliation TMDs thin films for improved electrocatalytic hydrogen evolution

This study explores a novel and efficient van der Waals thin-film deposition method, called Automatic Mechanical Exfoliation (AME), and its application in hydrogen evolution reaction (HER). Compared to traditional physical deposition techniques, AME offers significant advantages: it is simpler, more cost-effective, and significantly faster, enabling the deposition of large-area (>5 cm2) coatings exhibiting superior catalytic activity towards HER. To demonstrate its versatility, we comprehensively characterized large-area TMD thin films (MoS2/NbS2, NbS2, TiS2, MoSe2, MoS2, and WS2) using various techniques. Our AME-grown TMD thin films delivered improved HER performance, with lower Tafel slopes compared to previously reported values. To further enhance their activity, we irradiated the films with gamma radiation, leading to a remarkable improvement across all studied TMDs materials (e.g., an average increase of 30 % in exchange current density). Notably, NbS2 thin films and MoS2/NbS2 heterostructures exhibited excellent performance after irradiation, achieving low Tafel slopes (81 mV/dec and 85 mV/dec, respectively), starting overpotentials (−56 mV and −24 mV vs RHE, respectively), high exchange current densities (10.39 µA cm–2 and 625.2 µA cm–2, respectively), and turnover frequencies (0.021 s–1 and 0.95 s–1, respectively). These findings suggest that gamma irradiation can be a powerful tool for defect engineering in TMDs, creating additional active sites and demonstrably enhancing their catalytic efficiency for HER.

Constructing high efficient carrier channels in double ternary compounds MoSSe/CdSSe heterojunction for photoelectrochemistry and electrocatalytic hydrogen production

Here is a demonstration of constructing MoSSe/CdSSe heterojunction catalyst from bimetallic selenium sulfides. CdSSe has a high conduction band position of −0.65 eV, resulting in a strong reduction potential of photogenerated electrons. However, the high resistance of CdSSe affects the transport of charge carriers. In addition, experiments have confirmed that the presence of S and Se in MoSSe and CdSSe enhances their chemical activity and facilitates bonding. A better connection can be formed between MoSSe and CdSSe, resulting in high carrier transport efficiency. In the X-ray photoelectron spectroscopy results, the Mo and Se signals showed a large shift nearly 1 eV which confirms the strong binding between MoSSe and CdSSe. In the photoelectrochemical tests, the MoSSe/CdSSe heterojunction demonstrated a photocurrent density of 3.097 mA/cm2 at 0 V (RHE) which is 2.7 and 2.9 times that of MoSSe (1.227 mA/cm2) and CdSSe (1.127 mA/cm2) respectively with a low resistance of 161 Ω. Moreover, the MoSSe/CdSSe also has good electrocatalytic hydrogen evolution performance with an overvoltage of 180 mV and Tafel slope of 69 mV/dec. Fluorescence and photocurrent response tests confirmed its higher carrier separation efficiency. This work demonstrates the application of ternary metal selenium sulfide heterojunctions in catalytic energy materials.

High Mass Transfer Rate in Electrocatalytic Hydrogen Evolution Achieved with Efficient Quasi‐Gas Phase System

The adhesion of H2 bubbles on the electrode surface is one of the main factors limiting the performance of H2 evolution of electrolytic water, especially at high current density. To overcome this problem, here a "quasi‐gas phase" electrolytic water reaction system based on capillary effect is proposed for the first time to improve the mass transfer efficiency of H2. The typical feature of this reaction system is that the main site of H2 evolution reaction is transferred from the bulk aqueous solution to the gas phase environment above the bulk aqueous solution, thus effectively inhibiting the aggregation of H2 bubbles and reducing the resistance of their diffusion away. Electrochemical test results show that the proposed quasi‐gas phase system can significantly reduce the potential required in H2 evolution reaction process at high current density compared with the conventional electrolytic reaction system. Specifically, the overpotential potential is reduced by 0.31 V when the H2 evolution current density of 250 mA cm‐2 is achieved.

High Mass Transfer Rate in Electrocatalytic Hydrogen Evolution Achieved with Efficient Quasi-Gas Phase System.

The adhesion of H2 bubbles on the electrode surface is one of the main factors limiting the performance of H2 evolution of electrolytic water, especially at high current density. To overcome this problem, here a "quasi-gas phase" electrolytic water reaction system based on capillary effect is proposed for the first time to improve the mass transfer efficiency of H2. The typical feature of this reaction system is that the main site of H2 evolution reaction is transferred from the bulk aqueous solution to the gas phase environment above the bulk aqueous solution, thus effectively inhibiting the aggregation of H2 bubbles and reducing the resistance of their diffusion away. Electrochemical test results show that the proposed quasi-gas phase system can significantly reduce the potential required in H2 evolution reaction process at high current density compared with the conventional electrolytic reaction system. Specifically, the overpotential potential is reduced by 0.31 V when the H2 evolution current density of 250 mA cm-2 is achieved.

Complexes of a Noncyclic Carbazole-based N5-donor Schiff base: Structures, Redox, EPR and Poor Activity as Hydrogen Evolution Electrocatalysts.

A new noncyclic pentadentate N5-donor Schiff-base ligand, HL2Etpyr (1,1'-(3,6-ditert-butyl-9H-carbazole-1,8-diyl)bis(N-(2-(pyridin-2-yl)ethyl)methanimine)), prepared from 1,8-diformyl-3,6-ditertbutyl-carbazole (HUtBu) and two equivalents of 2-(2-pyridyl)ethylamine, along with four tetrafluoroborate complexes, [MIIL2Etpyr](BF4), where M = Co, Ni, Cu, and Zn, and two [CoIIL2EtPyr]·1/2[CoIIX4] complexes where X = NCS or Cl, isolated as solvates, are reported. All six complexes were structurally characterized, revealing the cations to be isostructural, with M(II) in a trigonal bipyramidal N5-donor environment. Only the Zn(II) complex is fluorescent. Cyclic voltammograms of [MIIL2Etpyr](BF4) in MeCN reveal reversible redox processes at positive potentials: 0.61 (Zn), 0.62 (Cu), 0.57 (Ni), and 0.25 V (Co), and for the cobalt complex a second quasi-reversible process occurs at 0.92 V vs Fc+/Fc. EPR data for the first oxidation product clearly demonstrate that the Zn complex undergoes a ligand centered oxidation, and support this being the case for the Ni and Cu complexes, although this is not definitively shown. After both oxidations the EPR data shows that the Co complex is best described as a low spin Co(III)-ligand radical. In the presence of 80 mM acetic acid, controlled potential electrolysis carried out on [MIIL2Etpyr](BF4) at -1.68 V in MeCN shows some electrocatalytic hydrogen evolution reaction (HER) performance in the order Ni(II) > Cu(II) > Co(II) - but the control, Ni(II) tetrafluoroborate, is more active than all three of the complexes.

Wafer Scale and Substrate-Agnostic Growth of MoS2 Nanowalls for Efficient Electrocatalytic Hydrogen Generation in Acidic and Alkaline Media

Emerging as a promising alternative to expensive platinum-based catalysts for electrocatalytic hydrogen evolution reaction (HER), molybdenum disulfide (MoS2) stands out for its favourable thermodynamic properties. However, the catalytic activity of MoS2 is mostly confined to its edges while the basal plane remains inactive, limiting practical applicability. Fabrication of stable MoS2 structures with enhanced active sites on a given surface area still remains a complex task. Here we introduce a substrate-agnostic, metal-organic chemical vapour deposition (MOCVD) method for large-area 3D dendritic nanostructures of 2D MoS2, termed as “MoS2 nanowalls”. Using scanning and transmission electron microscopy (SEM/TEM), we elucidate the growth mechanism of the MoS2 nanowalls and their branched dendritic structure. Even subjected to extreme pH environments (0 and 14) during the HER, the grown MoS2 nanowalls show remarkable stability even after >170hours of continuous operation and exhibit excellent catalytic activity with 10 mAcm-2 current density achievable by applying low overpotentials (309±2mV at pH = 0 and 272±2mV at pH = 14). The presented large-area growth method for inexpensive MoS2 nanowall based catalyst can pave the way for practical applications of water electrolysis cells operating at low voltages (≤1.5V).

Self-assembled formation of platinum single atoms and nanoclusters stabilized on MXene as an efficient catalyst for boosting electrocatalytic hydrogen evolution

Atomic isolated and dispersed single atom catalyst is ideal for high-performance industrial catalyst. However, the contribution from small amounts of nanoclusters coexisting with single atoms to the catalytic reaction activity is often neglected. In this work, a MXene-supported uniformly dispersed Pt single atoms and nanoclusters (Pt1+Ptn/MXene) were obtained by self-assembly through an impregnation method. The catalyst exhibits high electrochemical performance in the hydrogen evolution reaction with an overpotential of only 61.3 mV and a Tafel slope of 32.5 mV dec−1 at a current density of 10 mA cm−2 in an acidic environment. The XAFS analysis and further DFT calculation indicate that the synergistic effect between single atoms and nanoclusters can facilitate adsorption of H* and promote the HER reaction. This work provides an efficient method for integrating multiple active sites in noble metal catalysts.

Synergistic Heterostructural Interface of CoP and WC for High-Performance Wide pH-Universal Hydrogen Evolution Electrocatalysis

The development of cost-effective catalysts with high activity and stability over a wide pH range is urgent, but there are great challenges in the selection and design of catalyst materials. In this work, cobalt phosphide nanoparticles were modified onto tungsten carbide nanowire arrays (CoP@WC/CC) on carbon cloth substrate by a two-step method. The construction of CoP@WC heterostructure results in the downward shift of the d-band center, which optimizes the adsorption energy of catalyst and reaction intermediates. Meanwhile, the synergistic effect of CoP and WC contributes to the alkaline HER kinetic process. In addition, binder-free self-supporting nanoarray have excellent electrical conductivity, large specific surface area and strong structure, which is conducive to charge/matter exchange and catalyst stability. The results show that CoP@WC/CC can effectively drive HER over a wide pH range and exhibit better catalytic performance than the single component control sample. In 0.5 M H2SO4 and 1 M KOH, CoP@WC/CC can drive the current density of 10 mA cm-2 with only 52 and 70 mV, while showing excellent stability without obvious performance degradation during 100 hours of constant current test. A proton exchange membrane water electrolysis (PEMWE) using CoP@WC/CC catalyst operates stably for 200,000 s at 30 mA cm-2. This study provides a new reference for the design and development of high efficiency, low cost and wide pH-universal hydrogen evolution electrocatalysts.

Polytypic metal chalcogenide nanocrystals.

By engineering chemically identical but structurally distinct materials into intricate and sophisticated polytypic nanostructures, which often surpass their pure phase objects and even produce novel physical and chemical properties, exciting applications in the fields of photovoltaics, electronics and photocatalysis can be achieved. In recent decades, various methods have been developed for synthesizing a library of polytypic nanocrystals encompassing IV, III-V and II-VI polytypic semiconductors. The exceptional performances of polytypic metal chalcogenide nanocrystals have been observed, making them highly promising candidates for applications in photonics and electronics. However, achieving high-precision control over the morphology, composition, crystal structure, size, homojunctions, and periodicity of polytypic metal chalcogenide nanostructures remains a significant synthetic challenge. This review article offers a comprehensive overview of recent progress in the synthesis and control of polytypic metal chalcogenide nanocrystals using colloidal synthetic strategies. Starting from a concise introduction on the crystal structures of metal chalcogenides, the subsequent discussion delves into the colloidal synthesis of polytypic metal chalcogenide nanocrystals, followed by an in-depth exploration of the key factors governing polytypic structure construction. Subsequently, we provide comprehensive insights into the physical properties of polytypic metal chalcogenide nanocrystals, which exhibit strong correlations with their applications. Thereafter, we emphasize the significance of polytypic nanostructures in various applications, such as photovoltaics, photocatalysis, transistors, thermoelectrics, stress sensors, and the electrocatalytic hydrogen evolution. Finally, we present a summary of the recent advancements in this research field and provide insightful perspectives on the forthcoming challenges, opportunities, and future research directions.

Effects of Counter-Anions for the Engineering of Metallo-Hydrogels for Electrocatalytic Hydrogen and Oxygen Evolution Reactions

Effects of Counter-Anions for the Engineering of Metallo-Hydrogels for Electrocatalytic Hydrogen and Oxygen Evolution Reactions

Engineering a Ce Promoter into a Three-Dimensional Porous Mo2C@NC Heterostructure for Hydrogen Evolution Electrocatalysis via Weakening the Mo-H Bond Strength.

The pursuit of highly efficient electrocatalysts for the alkaline hydrogen evolution reaction (HER) is of paramount importance for water splitting. However, it is still a formidable task in Mo2C-based materials because of the agglomeration and strong Mo-H binding of Mo2C units. Herein, a novel CeOCl-CeO2/Mo2C heterostructure nesting within a three-dimensional porous nitrogen-doped carbon matrix has been designed and used for catalyzing HER via simultaneous morphology and heterointerface engineering. As expected, the optimal CeOCl-CeO2(0.2)/Mo2C@3DNC exhibits impressive HER activity, with a low overpotential of 156 mV at a current density of 10 mA cm-2 coupled with a slight Tafel slope of 62.20 mV dec-1. Introducing a Ce promoter, that is CeOCl and CeO2, would endow the interface with an internal electric field and electron redistribution between CeOCl-CeO2 and Mo2C induced by the heterogeneous work function difference. Moreover, experimental investigation and density functional calculations confirm that the CeOCl-CeO2/Mo2C heterointerface can downshift the d-band center of the active Mo center, weakening the strength of the Mo-H coupling. This proposed concept, engineering Ce-based promoters into active entities involved in the heterostructure to modulate intermediate adsorption, offers a great opportunity for the design of superior electrocatalysts for energy conversion.

Solution-Processable Microstructuring of 1T'-Phase Janus MoSSe Monolayers for Boosted Hydrogen Production.

Janus monolayers of transition metal dichalcogenides (TMDs) offer versatile applications due to their tunable polymorphisms. While previous studies focused on conventional 2H-phase Janus monolayers, the scalable synthesis of an unconventional 1T' phase remains challenging. We present a novel solution strategy for fabricating Janus 1T'-MoOSe and MoSSe monolayers by growing sandwiched Se-Mo-O/S shells onto Au nanocores. The Janus Au@1T'-MoSSe catalyst exhibits superior electrocatalytic hydrogen evolution reaction (HER) activity compared to 1T'-MoS2, -MoSe2, and -MoOSe, attributed to its unique electronic structure and intrinsic strain. Remarkably, photoexciting the nanoplasmonic Au cores further enhances the HER via a localized surface plasmon (LSP) effect that drives hot electron injection into surface sulfur vacancies of 1T'-MoSSe monolayer shells, accelerating proton reduction. This synergistic activation of anion vacancies by internal strain and external light-induced Au LSPs, coupled with our scalable synthesis, provides a pathway for developing tailorable polymorphic Janus TMDs for specific applications.

Bimetallic nanoalloys planted on super-hydrophilic carbon nanocages featuring tip-intensified hydrogen evolution electrocatalysis

The insufficient availability and activity of interfacial water remain a major challenge for alkaline hydrogen evolution reaction (HER). Here, we propose an “on-site disruption and near-site compensation” strategy to reform the interfacial water hydrogen bonding network via deliberate cation penetration and catalyst support engineering. This concept is validated using tip-like bimetallic RuNi nanoalloys planted on super-hydrophilic and high-curvature carbon nanocages (RuNi/NC). Theoretical simulations suggest that tip-induced localized concentration of hydrated K+ facilitates optimization of interfacial water dynamics and intermediate adsorption. In situ synchrotron X-ray spectroscopy endorses an H* spillover-bridged Volmer‒Tafel mechanism synergistically relayed between Ru and Ni. Consequently, RuNi/NC exhibits low overpotential of 12 mV and high durability of 1600 h at 10 mA cm‒2 for alkaline HER, and demonstrates high performance in both water electrolysis and chlor-alkali electrolysis. This strategy offers a microscopic perspective on catalyst design for manipulation of the local interfacial water structure toward enhanced HER kinetics.

Cu-doped Ni3S2 electrocatalyst for glycerol oxidation coupling to promote hydrogen evolution reaction

Hydrogen energy is becoming increasingly important as a clean and efficient form of energy. Glycerol oxidation synergistic electrocatalytic hydrogen evolution technology is an electrochemical process that integrates anodic glycerol oxidation reaction (GOR) and cathodic hydrogen production. Compared with the oxygen evolution reaction (OER) required in the electrolysis of water for hydrogen production process, this technology can not only reduce the energy consumption of the whole reaction, but also obtain valuable by-products while producing hydrogen. In this study, we successfully prepared a copper-doped Ni3S2 (Cu-Ni3S2@NF) electrode material loaded on a nickel foam carrier by a two-stage hydrothermal synthesis method, and applied it to the bifunctional electrocatalytic reaction of GOR and hydrogen evolution reaction (HER). After a series of in-depth electrochemical performance tests, it was confirmed that 0.1Cu-Ni3S2@NF showed lower overpotential requirements when performing GOR and HER, requiring only 1.41 V relative to the reversible hydrogen electrode (RHE) to drive a current density of 100 mA cm−2 for GOR, and only 0.56 V vs. RHE to achieve the same current density for HER. Moreover, the electrode material still maintains good stability under long-term operation. Among them, the Faraday efficiency (FE) of glycerol oxidation to formate is more than 85 %, while the FE of HER is not less than 93 %.

Simple generic self-assembly fabrication of transition metal borates on polyaminophenylboric acid modified foam nickel for highly-efficient overall water splitting

Water electrocatalysis for hydrogen production as a prospect strategy to store renewable energy and reduce carbon emissions has attracted great attention, and exploring water electrolysis catalysts has become a research hotspot for widespread industrial water electrolysis application. Very recently, transition metal borates have been demonstrated great potential for electrocatalytic hydrogen or oxygen evolution in alkaline media. However, a generic method for fabricating transition metal borates as bifunctional oxygen catalysts are still challenging. Herein, through a two-step process including poly-aminophenylboronic acid electrodeposition and subsequent electrostatic self-assembly of transitional metal ions, for the first time, to our best knowledge, a simple and generic approach to fabricate polyaminophenylborate transition metal salt modified nickel foam electrodes (PAB-M/NF, M represents transition metal element) was developed for highly efficient water splitting. As a proof of concept, the obtained PAB-Ru/NF exhibited remarkable bifunctional HER and OER catalytic activities and stability in alkaline medium. To drive the HER and OER with a current density of 10 mA cm−2 in 1 M KOH electrolyte, PAB-Ru/NF only required an overpotential of 14 mV and 301 mV, respectively. Moreover, even at a great current density of 250 mA cm−2, PAB-Ru/NF can exhibit very favorable long-term stability for over 35 h. When assembled into an electrolyzer with PAB-Ru/NF as both the anode and cathode, a current density of 10 mA cm−2 can be achieved at a very low cell voltage of 1.50 V. In addition, the other PAB-M/NF catalysts (M including but not limited to Fe, Co and Ni) prepared by the same way also show excellent bifunctional HER and OER catalytic activities and durability. This study provides a prospective and economically feasible generic approach for developing practical bifunctional catalysts for industrial water electrolysis.

Electrochemical investigations of chitosan/ZrO2-Bi2O3 composite for advanced energy and environmental applications

Energy needs are on the rise, and the need for effective corrosion resistance measures are also vital to meet the requirements prevailing in society. A multifunctional Chitosan/ZrO2-Bi2O3 composite is synthesized, keeping electrochemical analysis of energy and environmental applications in mind. Various physicochemical methods confirm the impact of integrating ZrO2-Bi2O3 into chitosan, resulting in improved efficacy across applications. The electrocatalytic supercapacitance, hydrogen evolution reaction, and corrosion inhibition studies are carried out to evaluate the efficiency of the synthesized composite. The composite shows a specific capacitance of 636.5 F/g, ensuring the effective utility for supercapacitance applications. The lower overpotential of 135.2 mV is shown by the composite in the electrocatalytic hydrogen evolution reaction. The synthesized composite also shows 96.2 % efficacy in corrosion inhibition studies. The studies conducted demonstrate the increased effectiveness of chitosan when combined with bimetal oxide. The chitosan composite is therefore a competent catalyst for energy and environmental applications.

(Invited) Two-Dimensional Layered Materials and Their Mixed-Dimensional Hybrids for Electrochemical Applications

Compared with their 3D counterparts, two-dimensional (2D) van der Waals (vdW) materials exhibit quantum confinement where charge carriers are spatially confined at the physical boundaries. Particularly, when mixing 2D materials with other low-dimensional (LD) materials, they exhibit enormous potential in electrochemical energy applications due to the unique properties arising from reduced dimensionality and, more importantly, material integration synergy.In this work, 2D transition metal dichalcogenides (MoS2) and their mixed low-dimensional hybrids (MLDHs) are introduced with an emphasis on the hybrid structure construction using the one-step solvothermal synthesis technique and their electrochemical applications. Fundamental insight into the synergistic effect of the MLDHs integration in terms of active site exposure, surface area enlargement, electrical conductivity improvement, and structural phase engineering for advancing the development of Li-ion batteries (LIBs) and electrocatalytic hydrogen evolution reaction (HER) will also be discussed. Specifically, in the case of LIBs, 2D-based binary hybrids (i.e., MoS2/MXene) deliver a Li-ion storage capacity of 540 mA h g−1 at 100 mA g−1 and a stable cycle performance up to 300 cycles. In sharp contrast, the 2D-based ternary MLDHs (i.e., MoS2/MXene/CNT) exhibit a higher Li-ion storage capacity (1500 mAh g−1 at 100 mA g−1), outstanding cycle stability (up to 300 cycles) and excellent rate capability (500 mAh g−1 at 4000 mA g−1) as an anode of LIBs. In the case of HER, the MLDH heterostructures show an overpotential of 169 mV with a low Tafel slope of 51 mV/dec and can be cycled to 1000 cycles. Leveraging the unique microreactor platform based on the 2D vdW platform, a mechanistic understanding of charge transport dynamics at the electrified electrode and current collector interface will be highlighted.The knowledge gained on how mixed-dimensional physics and chemistry will shed light on the design principle of the electrode materials for electrochemical energy storage and conversion and deepen the understanding of the process-structural-property-performance (PSPP) relationship of the vdW-based hybrid structures.

Engineered 2-D Heterostructures for Electrocatalysis

Atomically thin layered transition metal dichalcogenides (TMDs) such as MoS2, WS2, MoSe2 and WSe2 have been emerging as the cutting edge in materials science and engineering, due to their interesting electronic properties.1 These materials open up new opportunities for a variety of applications, including optoelectronics, energy conversion, and catalysis. To realize their potential device applications, it is highly desirable to achieve controllable growth of these layered nanomaterials, with tunable structure and morphology. TMDs exhibit promising catalytic properties for hydrogen generation and several approaches including defect engineering have been shown to increase the active catalytic sites.2,32D heterostructures based on various 2D layered materials with distinct properties have been demonstrated to exhibit novel physicochemical properties for their potential application in electrocatalytic hydrogen production. Here we present some of our efforts on morphological and photo/electrocatalytic studies of engineered 2D nanomaterials and their heterostructures.4-6 A seed-assisted chemical vapor transport (CVT) growth of ultra-thin triangular flakes of highly crystalline trigonal selenium (t-Se) oriented in (0001) direction, with lateral size >30 μm is demonstrated.[5,6] To study their promising photo-electrocatalytic properties and further realize the device applications, we employed a single-step CVT approach to grow selenene/WSe2 heterostructures. Vertical heterostructures of bi-layer selenene and monolayer WSe2 domains obtained via the CVT method are characterized by optical microscopy, transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and Raman spectroscopy. The micro electrocatalytic reactor fabricated with Se/WSe2 heterostructure shows significantly improved HER activities upon shining the light. The work further extends to explore strain-engineered TMDs and their heterostructures towards efficient electrocatalytic hydrogen evolution reaction. References H. R. Gutiérrez, N. Perea-López, A. L. Elías, A. Berkdemir, B. Wang, R . Lv, F. López-Urías, V. H. Crespi, H. Terrones, M. Terrones, Nano Lett. 2013, 13 (8), 3447-3454.P.V. Sarma, T.V.Vineesh, R.Kumar, V.Sreepal, R.Prasannachandran, A.K. Singh, and M.M. Shaijumon, ACS Catalysis(2020), 10,6753–6762P. V. Sarma, A. Kayal, C. H. Sarma, M. Thalakulam, J. Mitra, and M. M. Shaijumon, ACS Nano, 13, 10448-10455 (2019).R. Prasannachandran, T. V. Vineesh, A. Anil, B. M. Krishna and M. M. Shaijumon, ACS Nano, 12, 11511–11519 (2018).R. Prasannachandran, T. V. Vineesh, M.B.Lithin, R. Nandakishore, M. M. Shaijumon, Chem. Commun., 56, 8623-8626 (2020).P.V. Sarma, N. Renjith et al., 2D Mater., 9, 045004 (2022)

Nitrogen-Doped CoP-Co2P-Supported Ru with Interconnected Channels through a Microwave Quasi-Solid Approach for Hydrogen Evolution Reaction over a Wide pH Range.

Transition-metal phosphides (TMPs) have attracted extensive attention in energy-related fields, especially for electrocatalytic hydrogen evolution reaction (HER). However, it is imperative to develop a facile and time-consuming approach to prepare metal phosphides with satisfactory catalytic performance. Herein, nitrogen-doped CoP-Co2P decorated with Ru (Ru/N-CoP-Co2P) is synthesized (Ru/N-CoP-Co2P) through a hydrothermal route and following an ultrafast and simple microwave avenue within 20 s. The achieved Ru/N-CoP-Co2P possesses an interconnected porous morphology to expose abundant active sites and accelerate the mass transport. Moreover, N doping and Ru-supported decorated Ru/N-CoP-Co2P also play a key role in promoting the electrocatalytic activity. Therefore, the as-designed Ru/N-CoP-Co2P presents good catalytic performance for the HER in a wide pH range. Ru/N-CoP-Co2P merely needs overpotentials of 63, 100, and 65 mV to obtain 10 mA cm-2 in acidic, alkaline, and seawater electrolytes. This research provides a novel and efficient strategy for the synthesis of TMPs with highly efficient catalytic activity.