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Carbon materials/MXenes composite materials have gained widespread attention in the field of supercapacitors due to their excellent electrochemical performance. Carbon materials are considered ideal electrode materials for supercapacitors due to their high specific surface area, good conductivity, and outstanding electrochemical stability. MXenes, as a novel two-dimensional material, exhibit prominent conductivity, mechanical properties, and ionic conductivity, thereby showing great potential for applications in energy storage devices. The combination of carbon materials and MXenes is expected to fully leverage the advantages of both, optimizing electrode conductivity, enhancing the energy density and power density, and improving the charge–discharge performance. This article reviews the key research progress of carbon/MXenes composite materials in supercapacitors in recent years, including their synthesis methods, structural tuning, and improvements in their electrochemical performance. Finally, the article looks forward to future research directions and proposes potential strategies to enhance the overall performance of the composite materials and achieve large-scale applications. By addressing the existing challenges, carbon/MXenes composite materials are anticipated to achieve higher energy and power outputs for the supercapacitor field in the future, providing strong support for the development of new energy storage technologies such as electric vehicles and wearable devices. [ABSTRACT FROM AUTHOR]

p-Type YbCd2-xMgxSb2 (x = 0.1-0.8) Zintl phases are prepared by melting and annealing the elements (carbon crucible in evacuated quartz tube, 1. [ABSTRACT FROM AUTHOR]

Palladium–Platinum (Pd–Pt) alloys have excellent hydrogen isotope separation properties near room temperature compared to pure palladium (Pd), and are expected to be used as filling materials in thermal cyclic absorption (TCAP) columns. However, most studies on the thermodynamic and kinetic hydrogen isotope effects of hydrogen absorption/deuterium in Pd–Pt alloys have been conducted at temperatures of 273 K or above, with few studies involving the performance of TCAP in the cold-cycle operating temperature range (253 K–303 K). In this work, the performance of Pd-5wt.%Pt alloy for the absorption of hydrogen/deuterium at low temperatures (263 K–323 K) was investigated. The results show that the enthalpy and entropy of dissolution of hydrogen and deuterium in the α-phase of Pd-5wt.%Pt alloy are −11.77 kJ/mol (H), 104.00 J mol−1 K−1(H); −5.50 kJ/mol (D), 87.88 J mol−1 K−1 (D), respectively, which are lower than the enthalpy and entropy change values of pure Pd materials. The apparent reaction activation energies of protium and deuterium absorption are −4.14 kJ/mol (H 2) and −11.87 kJ/mol (D 2), respectively, which are lower than those of pure palladium. The excellent hydrogen isotope separation performance of Pd–Pt alloys may originate from the fast hydrogen absorption and discharge isotope kinetic performance. • The introduction of Pt affects the thermodynamic properties of palladium. • Catalytic dissociation of Pt and powder particle size affect the solid solution of Pd–Pt with hydrogen. • The Pt structure enhances the protium-deuterium separation at low H/Pd. • Negative apparent reaction activation energy for deuterium and deuterium absorption. [ABSTRACT FROM AUTHOR]

Review: 66 refs. [ABSTRACT FROM AUTHOR]

High-entropy alloy (HEA) nanomaterials have emerged as promising candidates as oxygen evolution reaction (OER) electrocatalyst to overcome the existing issues of the sluggish reaction kinetics and poor stability. In this study, Ir x RuCoCuNi HEA three-dimensional-nanoframeworks (3DNF) are prepared using a scalable approach-the spray-drying technique combined with thermal decomposition reduction (SD-TDR). The optimized catalyst, Ir 2 RuCoCuNi, demonstrates superior OER performance, with an overpotential of 264 mV at 10 mA cm -2 and a Tafel slope of 47 mV dec -1 , considerably surpassing the catalytic activity of commercial IrO 2 . Electrochemical data reveal high electron transfer efficiency and a significant electrochemically active surface area (ECSA), attributed to its 3DNF porous structure and favorable surface self-reconstruction into (oxy)hydroxides during the OER. While increasing Ir content enhances catalytic activity, economic analysis highlights compositions with reduced Ir content, such as IrRu 2 CoCuNi and IrRuCo 2 CuNi, as cost-effective alternatives for practical applications. These findings underscore the potential of HEA 3DNFs for industrial-scale electrocatalysis and provide insights into balancing performance and cost for next-generation OER catalysts., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Inc. All rights reserved.)