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The study examines the oxygen evolution reaction (OER) electrocatalytic efficiency of various stainless‐steel mesh (SSM) sizes in electrolytic cells. Stainless steel is chosen due to its widespread availability and stability, making it an economically viable option. The primary objective of this investigation is to determine the optimal stainless‐steel mesh size among those currently widely available on the market. The classification of stainless‐steel mesh sizes as SS304 is confirmed by the minimal compositional variations observed across all mesh sizes through electron dispersive X‐ray (EDX) spectra and X‐ray fluorescence (XRF) analyses. Remarkably, CV experiments carried out at different scan rates indicate that SSM 200 has the maximum specific electrochemical surface area (ECSA). As a result, SSM 200 demonstrates superior performance in terms of current density response and shows the lowest overpotential in the alkaline medium compared to other stainless‐steel mesh sizes. Furthermore, the SSM 200 exhibits a low overpotential of 337 mV at a current density of 10 mA/cm2 and a Tafel slope of 62.2 mV/decade, surpassing the performance of several previously reported electrodes for the OER. Stability tests conducted under constant voltage further confirm the remarkable stability of SSM 200, making it an ideal anode for electrolytic cell applications. These findings emphasize the cost‐effectiveness and high stability of SSM 200, presenting intriguing possibilities for future research and advancements in this field. [ABSTRACT FROM AUTHOR]

The practicality of the electrochemical CO2 reduction technique depends on the development of cost‐effective, robust, and highly selective catalysts. To achieve this goal, we have engineered self‐supported 3D electrodes composed of Pd‐Zn nanosheets (NSs) for CO2 electrochemical reduction to CO with minimal Pd content. This innovative electrode with an increased surface area was created using an electrodeposition method employing a dynamic hydrogen bubble template. By precisely adjusting the Pd content, we improved the thickness, porosity, and surface area of the electrodes, resulting in a CO2‐to‐CO selectivity reaching as high as 88.5 %, with an average of at least 80 % sustained over 10 hours. This remarkable improved activity can be attributed to the synergistic effects of an appropriate Pd/Zn atomic ratio as well as to the large surface area of nanosheets structures with rich edge active sites. Furthermore, to get around the limitations of CO2 mass transfer, reactions were done at high pressures conditions ranging from 3 to 9.5 bar; this strategic approach yielded an outstanding partial current density of −304.6 mA cm−2 for CO. These noteworthy findings establish concepts for constructing effective and earth‐abundant CO‐producing electrocatalysts. [ABSTRACT FROM AUTHOR]

Featured Application: Catalytic NOx emission control. Cu-CHA zeolites have proven to be effective for NOx reduction, but a drawback in using CHA zeolites is the cost associated with using expensive organic structure-directing agents. To overcome this drawback, we are reporting here the synthesis of Cu-CHA zeolite catalysts in both their NH4-form as well as K-form that do not require the use of organic structure-directing agents. After comprehensive characterization by XRF, XRD, 27Al NMR spectroscopy, FE-SEM, SEM/EDS, N2-adsorption/desorption, NH3-TPD, H2-TPR, and XPS, the zeolite catalysts were tested for NOx conversion by NH3-selective catalytic reduction (NH3-SCR). Cu-NH4-CHA zeolite catalysts exhibited remarkable activity and thermal stability over a wide temperature window, outperforming their counterpart K-forms. Among the NH4-forms of CHA zeolite catalysts, the 0.1 M Cu-NH4-CHA showed the best catalytic performance, achieving 50% NOx conversion at a temperature as low as 192 °C, and reaching full conversion of NOx at 261 °C. These Cu-based CHA zeolite catalysts are promising thanks to their environmentally friendly synthesis and offer the opportunity of maximizing DeNOx strategies in applications for NOx pollution abatement. [ABSTRACT FROM AUTHOR]

This article is a preface to a special issue of Chemistry - An Asian Journal that focuses on hydrogen production, storage, application, and sensing. It highlights the multifaceted nature of hydrogen and its potential as a transformative force in the global energy landscape. The article emphasizes the need for collaborative efforts from policymakers, industry stakeholders, and the scientific community to realize the full potential of hydrogen technologies. It discusses various aspects of hydrogen production, storage, application, and sensing, and presents valuable review articles and research papers on these topics. The article concludes by stating that the hydrogen economy presents a compelling energy transition strategy and calls for thorough research and innovative solutions in critical areas related to hydrogen. [Extracted from the article]