Titanium oxide (TiO₂) is a potential photocatalyst for removing toxic NO_x from the atmosphere. Its practical application is, however, significantly limited by its low absorption into visible light and a high degree of charge recombination. The overall photocatalytic activity of TiO₂ remains too low since it can utilize only about 4–5% of solar energy. Nitrogen doping into the TiO₂ lattice takes advantage of utilizing a wide range of solar radiation by increasing the absorption capability towards the visible light region. In this work, N-doped TiO₂, referred to as TC, was synthesized by a simple co-precipitation of tri-thiocyanuric acid (TCA) with P25 followed by heat treatment at 550 degrees C. The resulting nitrogen doping increased the visible-light absorption and enhanced the separation/transfer of photo-excited charge carriers by capturing holes by reduced titanium ions. As a result, TC samples exhibited excellent photocatalytic activities of 59% and 51% in NO oxidation under UV and visible light irradiation, in which the optimum mass ratio of TCA to P25 was found to be 10.

Hybrid supercapacitors (HSCs) have garnered growing interest for their ability to combine the high energy storage capability of batteries with the rapid charge–discharge characteristics of supercapacitors. This review examines the evolution of HSCs, emphasizing the synergistic mechanisms that integrate both Faradaic and non-Faradaic charge storage processes. Transition metal oxides (TMOs) are highlighted as promising battery-type electrodes owing to their notable energy storage potential and compatibility with various synthesis routes, including hydro/solvothermal methods, electrospinning, electrodeposition, and sol–gel processes. Particular attention is directed toward Ti-, Co-, and V-based TMOs, with a focus on tailoring their properties through morphology control, composite formation, and doping to enhance electrochemical performance. Overall, the discussion underscores the potential of HSCs to meet the growing demand for next-generation energy storage systems by bridging the gap between high energy and high power requirements.

Porous carbon is an emerging material for the capture of CO₂ from point sources of emissions due to its high structural, mechanical, and chemical stability, along with reusability advantages. Currently, research efforts are mainly focused on high- or medium-pressure adsorption, rather than low-pressure or DAC (direct air capture) conditions. Highly porous and functionalized carbon, containing heteroatoms (N, O, etc.), is synthesized using different activation synthesis routes, such as hard template, soft template, and chemical activation, to achieve high CO₂ capture efficiency at various temperatures and pressure ranges. Fundamental pore formation mechanisms with different activation routes have been evaluated and explored. Higher porosity alone can be ineffective without the presence of proper saturated diffusion pathways for CO₂ transfer. Therefore, it is imperative to emphasize more rational multi-hierarchical macro-/meso-/micro-/super-/ultra-pore design strategies to achieve a higher utilization efficiency of these pores. Moreover, the present research primarily focuses on powder-based hierarchical porous carbon materials, which may reduce the efficiency of the capture performance when shaping the powder into pellets or fixed-bed shapes for applications considered. Therefore, it is imperative to develop a synthesis strategy for pelletized porous carbon and to explore its mechanistic synthesis route and potential for CO₂ capture.

Gel-based materials have garnered significant interest in recent years, primarily due to their remarkable structural flexibility, ease of modulation, and cost-effective synthesis methodologies. Specifically, polymer-based conductive gels, characterized by their unique conjugated structures incorporating both localized sigma and pi bonds, have emerged as materials of choice for a wide range of applications. These gels demonstrate an exceptional integration of solid and liquid phases within a three-dimensional matrix, further enhanced by the incorporation of conductive nanofillers. This unique composition endows them with a versatility that finds application across a diverse array of fields, including wearable energy devices, health monitoring systems, robotics, and devices designed for interactive human-body integration. The multifunctional nature of gel materials is evidenced by their inherent stretchability, self-healing capabilities, and conductivity (both ionic and electrical), alongside their multidimensional properties. However, the integration of these multidimensional properties into a single gel material, tailored to meet specific mechanical and chemical requirements across various applications, presents a significant challenge. This review aims to shed light on the current advancements in gel materials, with a particular focus on their application in various devices. Additionally, it critically assesses the limitations inherent in current material design strategies and proposes potential avenues for future research, particularly in the realm of conductive gels for energy applications.

Rechargeable lithium–sulfur batteries (LSBs) are emerging as some of the most promising next-generation battery alternatives to state-of-the-art lithium-ion batteries (LIBs) due to their high gravimetric energy density, being inexpensive, and having an abundance of elemental sulfur (S₈). However, one main, well-known drawback of LSBs is the so-called polysulfide shuttling, where the polysulfide dissolves into organic electrolytes from sulfur host materials. Numerous studies have shown the ability of porous carbon as a sulfur host material. Porous carbon can significantly impede polysulfide shuttling and mitigate the insulating passivation layers, such as Li₂S, owing to its intrinsic high electrical conductivity. This work suggests a scalable and straightforward one-step synthesis method to prepare a unique interconnected microporous and mesoporous carbon framework via salt templating with a eutectic mixture of LiI and KI at 800 °C in an inert atmosphere. The synthesis step used environmentally friendly water as a washing solvent to remove salt from the carbon–salt mixture. When employed as a sulfur host material, the electrode exhibited an excellent capacity of 780 mAh g⁻¹ at 500 mA g⁻¹ and a sulfur loading mass of 2 mg cm⁻² with a minor capacity loss of 0.36% per cycle for 100 cycles. This synthesis method of a unique porous carbon structure could provide a new avenue for the development of an electrode with a high retention capacity and high accommodated sulfur for electrochemical energy storage applications.