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In this manuscript, a comprehensive study is presented on Fe-based electrocatalysts with mono, bi, and tri-metallic compositions, emphasizing the influence of processing-structure correlations on the electrocatalytic activity for the oxygen reduction reaction (ORR) in the alkaline medium. These electrocatalysts were synthesized through the mixing of transition metal phthalocyanines (TM-Pc) with conductive carbon support, followed by controlled thermal treatment at specific temperatures (600 °C and 900 °C). An extensive analysis was conducted, employing various techniques, including X-ray Absorption Spectroscopy (XAS), Transmission Electron Microscopy (TEM), and X-ray Diffraction (XRD), providing valuable insights into the structural characteristics of the synthesized nanoparticles. Importantly, an increase in the Fe-Pc weight percentage from 10% to 30% enhanced the ORR activity, although not proportionally. Furthermore, a comparative analysis between mono, bi, and tri-metallic samples subjected to different functionalization temperatures highlighted the superior electrocatalytic activity of electrocatalysts functionalized at 600 °C, particularly Fe 600 and Fe-Ni-Cu 600. These electrocatalysts featured Eon values of 0.96 V vs. RHE and E1/2 values of 0.9 V vs. RHE, with the added benefit of reduced anionic peroxide production. The potential of these Fe-based electrocatalysts to enhance ORR efficiency is underscored by this research, contributing to the development of more effective and sustainable electrocatalysts for energy conversion technologies.

Hydrogen is considered as one of the key energy carrier for the forthcoming green transition because of its high energy content and harmless combustion products. Water electrolysis, powered by green electricity, is one of the most efficient and promising technologies for H2 production. Cheap and earth abundant metals-based electrocatalysts for Hydrogen Evolution Reaction (HER) are needed to drive a green transition based on hydrogen produced by water electrolysis. Perforated plate type Ni electrodes are prepared by a cost-effective electroforming process, designed to work for water electrolysis in alkaline environment in a flow-through configuration facilitating the release of bubbles produced by HER. The aim of this work is to synthesize a catalyst layer based on NiCuMo alloy produced by an electrodeposition process tailored to maximize electrocatalytic performances, increasing the electrochemical surface active area (more than 50 times) and its activity. HER is studied in aqueous 1 M KOH solution and an overpotential of only 95 mV is measured to reach 100 mA cm−2, assessing a Tafel slope of 61 mV dec−1. 100 h durability test is successfully carried out demonstrating the high chemical and mechanical stability of so-prepared electrodes for next generation alkaline electrolyzers.

In this work, platinum group metal-free (PGM-free) electrocatalysts were synthesized, characterized, and tested for hydrogen evolution reaction (HER). These materials were mono-, bi- and trimetallic Ni-based electrocatalysts with the addition of a second or a third transition metal (TM), such as iron and cobalt. TM–phthalocyanine (TMPc) was used as a metal precursor, mixed with a conductive carbon backbone and subjected to pyrolysis under controlled temperature and atmosphere conditions. Two temperatures of pyrolysis (600 °C and 900 °C) were used. The effect of TM loading in the precursors, different pyrolysis temperatures on the surface chemistry and morphology, and electrocatalytic activity towards HER were evaluated. The increase of NiPc in the initial mixture is beneficial to improving the electrocatalytic activity. The addition of a second and a third metal reflects positively on the HER performance. Interestingly, the pyrolysis temperature influences both the formation and growth of the nanoparticles, and this information is supported by high-resolution transmission electron microscopy (HR-TEM) and light synchrotron X-ray absorption spectroscopy (XAS) measurements.

Fuel cell heavy-duty vehicles (HDVs) require increased durability of oxygen-reduction-reaction electrocatalysts, making knowledge of realistic degradation mechanisms critical. Here identical-location micro-X-ray fluorescence spectroscopy was performed on membrane electrode assemblies. The results exposed heavy in-plane movement of electrocatalyst after HDV lifetime, suggesting that electrochemical Ostwald ripening may not be a local effect. Development of local loading hotspots and preferential movement of electrocatalyst away from cathode catalyst layer cracks was observed. The heterogeneous degradation exhibited by a modified cathode gas diffusion layer membrane electrode assembly after HDV lifetime was successfully quantified by the identical-location approach. Further synchrotron micro-X-ray diffraction and micro-X-ray fluorescence experiments were performed to obtain the currently unknown correlation between electrocatalyst nanoparticle size increase and loading change. A direct correlation was discovered which developed only after HDV lifetime. The work provides a route to engineer immediate system-level mitigation strategies and to develop structured cathode catalyst layers with durable electrocatalysts. [Figure not available: see fulltext.]

Direct methanol fuel cells (DMFCs) are promising electrochemical systems capable of producing electricity from the electrochemical oxidation of methanol and the reduction of oxygen. In this work, the effectiveness of the addition of sulfuric acid as a supporting electrolyte for methanol fuel composition was assessed. The results showed that the peak of power curve in DMFCs with Pt/C cathode electrocatalysts increased progressively from 70 mW cm−2 (0 mM of H2SO4) to 115 mW cm−2 with a concentration of 100 mM of H2SO4. These results underlined the positive effect of the addition of a supporting electrolyte in the methanol aqueous solution on the electrochemical output that was enhanced. Platinum group metal-free (PGM-free) electrocatalysts based on Fe-Nx-C type were also tested being insensitive to methanol crossover and oxidation at the cathode. DMFC with Fe–N–C cathode catalysts result in a performance of 21.5 mW cm−2. In these operating conditions, the addition of supporting electrolyte does not seem to bring excessive advantage. Short stability tests are presented and an overall assessment of the resistances within the system is also discussed.

Four different C 3 N 4 specimens have been prepared, a bulk one (MCN), a thermally etched (MCN-TE), a solid prepared by hydrothermally treating MCN with H 2 O 2 (MCN-H 2 O 2 ) and a polymeric carbon nitride-hydrogen peroxide adduct (MCN-TE-H 2 O 2 ). The principal aim of this work was to correlate the capability of the prepared material to generate reactive oxygen species (ROS), under irradiation, with their photocatalytic activities in terms of conversion and selectivity for partial oxidation reactions. Photoelectrochemical studies revealed that MCN-TE represented the best material in terms of photoconductivity, whereas MCN-H 2 O 2 was defective and evidenced a poor mobility of carriers. EPR studies showed a maximum generation of reactive oxygen species irradiating the MCN-TE sample. The photocatalytic activity of these materials in the selective oxidation of three different alcohols to the corresponding aldehydes, both under UV and natural solar light, showed that the highest conversion was obtained in the presence of the MCN-TE sample, whereas the most selective one was MCN-TE-H 2 O 2 . Under solar light irradiation the performances of the powders were generally better than those under UV light. The characterization of the C 3 N 4 -based materials well justified their photocatalytic activity. The pristine C 3 N 4 materials were more active but less selective than those prepared in the presence of H 2 O 2 .

We investigate the modal logic of stepwise removal of objects, both for its intrinsic interest as a logic of quantification without replacement, and as a pilot study to better understand the complexity jumps between dynamic epistemic logics of model transformations and logics of freely chosen graph changes that get registered in a growing memory. After introducing this logic ($\textsf{MLSR}$) and its corresponding removal modality, we analyze its expressive power and prove a bisimulation characterization theorem. We then provide a complete Hilbert-style axiomatization for the logic of stepwise removal in a hybrid language enriched with nominals and public announcement operators. Next, we show that model-checking for $\textsf{MLSR}$ is PSPACE-complete, while its satisfiability problem is undecidable. Lastly, we consider an issue of fine-structure: the expressive power gained by adding the stepwise removal modality to fragments of first-order logic.

Polymeric C3N4 and O-doped C3N4: Photoelectrochemical and EPR Features for Selective Photocatalytic Oxidation of Alcohols to Aldehydes