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Trimetallic nickel–iron–molybdenum oxides are excellent electrocatalysts for alkaline water electrolysis despite experiencing severe molybdenum dissolution. While the impact of molybdenum on fresh samples is well-understood, its substantial loss during operation without compromising performance presents a unique puzzle. Here, we show that the initial presence of molybdenum induces the formation of nickel vacancies and distorts octahedral nickel sites. This structural distortion induces charge transfer between lattice oxygen and nickel, inducing an early formation and stabilization of active nickel oxyhydroxides. Even after complete molybdenum leaching and transitioning into a bimetallic nickel-iron oxide, the catalyst retains its exceptional performance due to the persistence of distorted octahedral nickel sites. Understanding this process enables the exploration of alternative metals that could induce similar structural distortions, as well as inspire similar strategies in other electrocatalysts. (Figure presented.)

The increasing demand for green hydrogen is driving the development of efficient and durable electrocatalysts for the hydrogen evolution reaction (HER). Nickel-molybdenum (NiMo) alloys are among the best HER electrocatalysts in alkaline electrolytes, and here we report a scalable solution precursor plasma spraying (SPPS) process to produce the highly active Ni4Mo electrocatalysts directly onto metallic substrates. The NiMo coating coated onto inexpensive Ni mesh revealed an excellent HER performance with an overpotential of only 26 mV at −10 mA cm⁻² with a Tafel slope of 55 mV dec⁻¹. Excellent operational stability with minimum changes in overpotential were also observed even after extensive 60 hour high-current stability test. In addition, we investigate the influence of different substrates over the catalytic performance and operational stability. We also proposed that a slow, but consistent, dissolution of Mo is the primary degradation mechanism of NiMo-based coatings. This unique SPPS approach enables the scalable production of exceptional NiMo electrocatalysts with remarkable activity and durability, positioning them as ideal cathode materials for practical applications in alkaline water electrolysers.

MoS₂ is widely praised as a promising replacement for Pt as an electrocatalyst for the hydrogen evolution reaction (HER), but even today, it still suffers from low performance. This issue is tackled by using Mn³⁺ as a surface modifier to trigger sulfur vacancy formation and enhance electron transport in few-layered 2H MoS₂. Only 10% of Mn is sufficient to transform the semiconductive MoS₂ into an active HER electrocatalyst. The insertion of Mn reduces both HER onset potential and Tafel slope which allows reaching 100 mA/cm² at an overpotential of 206 mV, ten times larger of what undoped MoS₂ can achieve. The enhanced activity arises because Mn³⁺ introduces electronic states near the conduction band, promotes sulfur vacancies, and increases the hydrogen adsorption. In addition to its facile production and extended shelf-life, Mn–MoS₂ exhibits an efficiency of 73% at 800 mA/cm² and 2.0 V when used in proton exchange membrane water electrolyzers.

Robust electrocatalysts required to drive the oxygen evolution reaction (OER) during water electrolysis are still a missing component toward the path for sustainable hydrogen production. Here a new family of OER active quaternary mixed-oxides based on X-Sn-Mo-Sb (X = Mn, Fe, Co, or Ni) is reported. These nonstoichiometric mixed oxides form a rutile-type crystal structure with a random atomic motif and diverse oxidation states, leading to the formation of cation vacancies and local disorder. The successful incorporation of all cations into a rutile structure was achieved using oxidizing agents that facilitates the formation of Sb⁵⁺ required to form the characteristic octahedral coordination in rutile. The mixed oxides exhibit enhanced stability in both acidic and alkaline environments under anodic potentials with no changes in their crystal structure after extensive electrochemical stress. The improved stability of these mixed oxides highlights their potential application as scaffolds to host and stabilize OER active metals.

Proton exchange membrane water electrolysis is widely used in hydrogen production, but its application is limited by significant electrocatalyst dissolution at the anode during the oxygen evolution reaction (OER). The best performing electrocatalysts to date are based on ruthenium and iridium oxides, but these experience degradation even at moderate cell potentials. Here we investigate a quaternary Sn-Sb-Mo-W mixed oxide as a protective scaffold for ruthenium oxide. The acid-stable mixed oxide consists of an interconnected network of nanostructured oxides capable of stabilizing ruthenium into the matrix (Ru-MO). In combination with titanium fibre felt, we observed a lower degradation in the oxygen evolution reaction activity compared to unprotected ruthenium oxide after the electrochemical stress test. The superior stability of Ru-MO@Ti is attributed to the presence of MO which hinders the formation of reactive higher valence ruthenium (Ru+8). Our work demonstrates the potential of multi-metal oxides to extend the lifetime of the OER active metal and the titanium support.

Proton exchange membrane water electrolysis (PEMWE) is a promising technology to produce high-purity renewable hydrogen gas. However, its operation efficiency is highly dependent on the usage of expensive noble metals as electrocatalysts. Replacing, decreasing, or simply extending the operational lifetime of these precious metals have a positive impact on the hydrogen economy. Mo-based electrocatalysts are often praised as potential materials to replace the Pt used at the cathode to catalyse the hydrogen evolution reaction (HER). Most electrocatalytic studies are performed in traditional three-electrode cells with different operational conditions than those seen in PEM systems, making it difficult to predict the expected material’s performance under industrially relevant conditions. Therefore, we investigated the viability of using three selected Mo-based nanomaterials (1T′-MoS2, Co-MoS2, and β-Mo2C) as HER electrocatalysts in PEMWE systems. We investigated the effects of replacing Pt on the catalyst loading, charge transfer resistance, kinetics, operational stability, and hydrogen production efficiency during the PEMWE operation. In addition, we developed a methodology to identify the individual contribution of the anode and cathode kinetics in a PEMWE system, allowing to detect the cause behind the performance drop when using Mo-based electrocatalysts. Our results indicate that the electrochemical performance in three-electrode cells might not strictly predict the performance that could be achieved in PEMWE cells due to differences in interfaces and porosity of the macroscopic catalyst layers. Among the catalysts studied, 1T′-MoS2 is truly an excellent candidate to replace Pt as an HER electrocatalyst due to its low overpotential, low charge transfer resistance, and excellent durability, reaching a high efficiency of ∼75% at 1 A cm-2 and 1.94 V. Our study highlights the importance of a continuous development of efficient noble-metal free HER electrocatalysts suitable for PEMWE systems.

The creation of effective Pd-based architectures with numerous electrocatalytic active sites and efficient charge transfer is of key importance for improving the electrocatalytic performance in water electrolyzer and fuel cell applications. On the other hand, MoS2, possessing multiple electrocatalytic active sites, can act both as support and booster to Pd-based electrocatalytic structures. Herein, MoSx@Pd hybrids were successfully synthesized by using a one-pot liquid phase solvothermal strategy with stoichiometric excess of Pd. The optimized MoSx@Pd proves to be an excellent bifunctional electrocatalyst for both hydrogen evolution reaction and oxygen reduction reaction (ORR). Optimized MoSx@Pd operates the process for hydrogen evolution at the same potential as Pt/C and achieves a low overpotential of 76 mV at −10 mA cm−2 due to improved reaction kinetics and charge transfer processes between Pd and MoS2. On top of that, MoSx@Pd exhibits excellent performance and stability as cathode electrocatalyst in a polymer electrolyte membrane water electrolyzer. Simultaneously, the bifunctional electrocatalyst shows enhanced electrocatalytic ORR activity and stability by maintaining 93% of its initial activity outperforming commercial Pt/C. Finally, rotating ring disk electrode analysis reveals that ORR proceeds through the energy efficient 4e− pathway, with water being the main product, rendering MoSx@Pd a promising component for fuel cells.

Foam-like NiMo coatings were produced from an inexpensive mixture of Ni, Al, and Mo powders via atmospheric plasma spraying. The coatings were deposited onto stainless-steel meshes forming a highly porous network mainly composed of nanostructured Ni and highly active Ni₄Mo. High material loading (200 mg cm⁻²) with large surface area (1769 cm² per cm²) was achieved without compromising the foam-like characteristics. The coatings exhibited excellent activity towards both hydrogen evolution (HER) and oxygen evolution (OER) reactions in alkaline media. The HER active coating required an overpotential of 42 mV to reach a current density of −50 mA cm⁻² with minimum degradation after a 24 h chronoamperometry test at −10 mA cm⁻². Theoretical simulations showed that several crystal surfaces of Ni4Mo exhibit near optimum hydrogen adsorption energies and improved water dissociation that benefit the HER activity. The OER active coating also consisting of nanostructured Ni and Ni₄Mo required only 310 mV to achieve a current density of 50 mA cm⁻². The OER activity was maintained even after 48 h of continuous operation. We envisage that the development of scalable production techniques for Ni₄Mo alloys will greatly benefit its usage in commercial alkaline water electrolysers.

Graphene oxide (GO) is a 2D nanomaterial with unique chemistry due to the combination of sp2 hybridization and oxygen functional groups (OFGs) even in single layer. OFGs play a fundamental role in the chemical functionalization of GO to produce GO-based materials for diverse applications. However, traditional strategies that employ epoxides, alcohols, and carboxylic acids suffer from low control and undesirable side reactions, including by-product formation and GO reduction. Thiol-ene “click” reaction offers a promising and versatile chemical approach for the alkene functionalization (−C=C−) of GO, providing orthogonality, stereoselectivity, regioselectivity, and high yields while reducing by-products. This review examines the chemical functionalization of GO via thiol-ene “click” reactions, providing insights into the underlying reaction mechanisms, including the role of radical or base catalysts in triggering the reaction. We discuss the “how” and “where” the reaction takes place on GO, the strategies to avoid unwanted side reactions, such as GO reduction and by-product formation. We anticipate that multi-functionalization of GO via the alkene groups will enhance GO physicochemical properties while preserving its intrinsic chemistry.

Thiol-ene radical addition (TERA) is a powerful reaction for the chemical functionalization of the reactive alkenes of GO with thiols. To trigger TERA, a photoinitiator (PI) is added to ensure high yields associated with fast conversion rates. However, the inappropriate use of PIs might affect the GO functionalization leading to photoreduction as well as low conversion rates. Herein, we explored the GO functionalization with cysteamine (CA) by TERA and its reduction influenced by Irgacure® 369, a commercial PI. We focused to analyze the reaction conditions that promote an orthogonal GO functionalization finding the limits where the photoreduction began. UV-spectroscopy, Raman spectroscopy, fluorescence labeling and XPS were used to characterize the functionalized GO. The data indicate three possible scenarios depending on the PI/CA molar ratio: i) orthogonal GO functionalization by TERA, ii) side reactions between GO and the radicals formed upon the PI photocleavage, and iii) soft photoreduction of the GO with alcohols and carboxylic acids as the functional groups mainly affected. However, we found that the GO functionalization by TERA was still occurring, but in less favorable conditions despite the side reactions and by-products. Therefore, photo-initiated TERA was confirmed as a powerful reaction to functionalize the reactive alkenes of GO, and by tuning the PI/CA molar ratio an orthogonal GO functionalization can be achieved, limiting side reactions and particularly GO reduction.