Nanoenergy Adv., Volume 6, Issue 1 (March 2026) – 9 articles

It is of great significance to prepare carbon-supported non-noble metal catalysts for hydrogen evolution reaction (HER) via a sustainable method. Meanwhile, the enhanced metal-support interaction (MSI) is vital for promoting the catalytic activity of metal/carbon catalysts. Herein, we prepare a biomass-derived porous carbon-supported metal Ni catalyst (Ni/APC) with the enhanced MSI via atomic Ni-N₄ sites utilizing agaric as a precursor. The highly dispersed Ni-N₄ species preferentially adsorb dye molecules and reactant H₂O, beneficial to efficient electron transfer and promoting H₂O dissociation. Meanwhile, Ni nanoparticles undertake the active sites for H₂ desorption. In virtue of the synergistic effect of metal Ni nanoparticles and atomic Ni-N₄ for different roles of active sites, Ni/APC catalysts show more effective dye-sensitized photocatalytic HER activities, compared with pure Ni and pure APC. The Ni/APC catalyst with an optimal Ni loading amount exhibits a high AQY of 41.0% with an excellent long-term stability in terms of both HER activity and structure. It is the first report of an application for biomass-derived carbon catalysts in dye-sensitization hydrogen production, and the synergistic effect of atomic Ni and particled Ni on the dye-sensitized photocatalytic HER is deeply investigated. This work provides new deep insight into the design of new non-noble metal/carbon materials by taking advantage of biomass materials. Full article

Energy obtained by green ways with releasing environmental pollution is still a challenge for sustainable development for model society. Among energy technologies, photothermal conversion by using solar energy has become a new field and a hot topic in recent years. Based on the exploration of nanomaterials in the past decades, photothermal nanomaterials by using nanomaterials bring new chances for expending the utilization of green energy with high efficiency, mainly including metal semiconductors and carbon nanomaterials. Their modulated structure for enhancing light absorption, accelerating transformation of photon into heat, and located heat management were also considered important for promoting the utilization of solar energy and therefore, the strategies for designed and controllable preparing of photothermal nanomaterials were also summarized. The applications of photothermal nanomaterials were also reviewed to reveal the new chances for energy conversion engineering or promoting the solar energy utilization of solar energy in some cold regions or somewhere with low solar irradiation. Full article

Rechargeable zinc–air batteries (ZABs) are still impeded by the intrinsically sluggish kinetics of oxygen reduction and evolution reactions (ORR/OER) and by the instability or prohibitive price of state-of-the-art noble metal catalysts. Metal–organic frameworks (MOFs) have recently emerged as versatile sacrificial templates for next-generation air–cathode electrocatalysts. By programming pyrolytic or chemical conversion pathways, MOFs can be quantitatively transformed into hierarchically porous, heteroatom-doped carbon scaffolds that embed uniform metal, alloy, or metal-oxide nanodomains. The resulting architectures couple metallic conductivity with molecular-scale active site tunability, delivering exceptional ORR/OER activity, stability, and mass transport properties. This review critically examines the most recent advances in MOF-derived electrocatalysts for ZABs, establishing quantitative structure–composition–performance relationships across mono-, bi-, and multi-metallic systems. Emphasis is placed on deciphering how framework topology, metal–ligand coordination, and post-synthetic parameters dictate the density, electronic structure, and accessibility of surface-active moieties during catalyst evolution. We further dissect engineering strategies that enhance intrinsic activity via electronic modulation, bolster durability through encapsulation effects, and optimize hierarchical porosity for rapid O₂/water transport. This article concludes by outlining unresolved challenges and future research directions, including atomically precise active site construction, multi-scale compositional control, long-term reversibility under realistic ZABs cycles, scalable and green synthesis, providing a roadmap for translating MOF-derived catalysts from laboratory curiosities to commercially viable air–cathode materials. Full article

The emergence of advanced low-dimensional materials of the graphene family opens up unique opportunities for energy-efficient and fast processing of electrical and optical signals in a wide spectral range from ultraviolet to infrared. Non-volatile resistive states in memristors based on two-dimensional (2D) crystals, 1D nanoribbons, and 0D quantum dots are accessible for control by light and an electric field due to polarization and rearrangement of sp²-sp³ hybridization of carbon atoms, as well as due to photoinduced phase transitions. Two-dimensional materials possess unique structural and electronic properties required for the development of highly efficient nanoenergy memristor devices for low-energy information technology. This article discusses memristors and photomemristors based on graphene, graphene oxide, diamane, and chalcogenide semiconductors such as MoS₂, WSe₂, MoS_2−xO_x, which are structurally similar to graphene and have a 2D layered structure. Memristors based on graphene and graphene oxide, bigraphene, and diamane, fabricated using localized electron irradiation, exhibit nonlinear behavior and well-controlled memristive states associated with sp²-sp³ transitions of carbon atoms under low-power conditions. The review highlights the dual role of graphene as an active material and electrode, as well as the redox control mechanism. Due to a well-controlled redox process, graphene-based devices exhibit the dynamic behavior required for neuromorphic computing directly in the sensor, reducing the energy and time costs associated with data processing. Neuromorphic computing in a photomemristor-based sensor enables the creation of a compact nano-energy system for real-time information recognition in a wide spectral range, similar to biological vision, for use in self-driving cars, personalized medicine, and other applications. Full article

The increasing global energy demand and its negative environmental impact created the need for substantial changes in the energy infrastructure. A hydrogen-based infrastructure appears to be the most promising way to secure a clean and safe energy future. Water electrolysis is a method that can be used to generate green hydrogen, but suitable electrocatalysts are required for large-scale applications. This work investigates the electrocatalytic activity of electrodes modified with novel TiO₂ nanotube-based electrocatalysts for water electrolysis. The focus was on the hydrogen evolution reaction (HER), and the electrodes that displayed the highest activity were the ones obtained with the procedure consisting of the growth of TiO₂ nanotubes on a Ti plate by anodization, the subsequent deposition of MoO₂ and Ni(OH)₂, and a thermal treatment performed under different conditions. The results of the HER experiments performed in a strong alkaline environment showed that the electrode obtained via vacuum heat treatment exhibited the lowest overpotential value, of 238 mV at i = −10 mA/cm². Furthermore, the electrode was electrochemically stable, and inter-electrode reproducibility tests revealed only a small variation of the HER overpotential. Full article

Freshwater scarcity is increasing day by day and has already reached a threatening level, especially in remotely populated areas. One of the technological solutions to this rising concern could be the use of the solar-based humidification–dehumidification (SHDH) method for water desalination. This technology is a promising solution but has challenges such as solar intermittency. This challenge can be solved by integrating SHDH with the phase change material as a solar energy storage medium. Therefore, a novel nano-enhanced binary eutectic phase change material (NEPCM) was developed in this project. PCM consisting of 70 wt.% stearic acid (ST) and 30 wt.% suberic acid (SBU) with a varying concentration of silicon carbide (SiC) nanoparticles (NPs) (0.1 to 3 wt.%) was synthesized specifically considering the need of SHDH application. The systematic thermophysical characterization was conducted to investigate their energy storage capacity, thermal durability, and performance consistency over repeated cycles. DSC analysis revealed that the addition of SiC NPs preserved the thermal stability of the NEPCM, while the phase transition temperature remained nearly unchanged with a variation of less than 0.74%. The value of latent heat is inversely related to the nanoparticle concentration, i.e., from 142.75 kJ/kg for the base PCM to 131.24 kJ/kg at 3 wt.% loading. This corresponds to reductions in latent heat ranging between 0.98% and 8.06%. The FTIR measurement confirms that no chemical reactions or no new functional groups were formed. All original functional groups of ST and SBU remained intact, showing that incorporating the SiC NP to the PCM lead to physical interactions (e.g., hydrogen bonding or surface adsorption). The TGA analysis showed that the SiC NPs in the NEPCM act as supporting material, and its nano-doping enhanced the final degradation temperature and thermal stability. There was negligible change in thermal conductivity for nanoparticle loadings of 0.1% and 0.4%; however, it increased progressively by 5.2%, 10.8%, 23.12%, and 25.8% at nanoparticle loadings of 0.7%, 1%, 2%, and 3%, respectively, at 25 °C. Thermal reliability was analyzed through a DSC thermal cycling test which confirmed the suitability of the material for the desired applications. Full article

High-temperature proton exchange membrane systems (HT-PEM) based on polybenzimidazole (PBI) membranes are a promising technology offering significant advantages over their low-temperature counterparts. A key challenge limiting its long-term durability is the leaching of phosphoric acid (PA) from the membrane during operation. This work introduces, for the first time, the strategy of modifying polybenzimidazole (PBI) membranes with amino-functionalized porous aromatic frameworks (PAF-20-NH₂) to fundamentally enhance their PA retention and operational stability, a critical challenge for high-temperature PEM technologies. We propose that the synergistic combination of the framework’s nanoscale porosity and the specific interaction of its amino groups create an unprecedented network for acid immobilization via reinforced hydrogen bonding. A comprehensive study of the membranes’ physicochemical and structural properties reveals that PAF-20-NH₂ modification results in a significant and quantitatively demonstrated improvement in acid retention capacity, directly translating into a notable increase in proton conductivity compared to both pristine PBI and membranes modified with the non-functionalized PAF-20. These findings establish a new, highly effective pathway for the rational design of next-generation high-performance PBI-based membranes. Full article

This review examines modern approaches to layer formation in solid oxide fuel cells (SOFCs), focusing on traditional, thin-film, and additive manufacturing methods. A systematic comparison of technologies, including slip casting, screen printing, CVD, PLD, ALD, HiPIMS, inkjet, aerosol, and microextrusion printing, is provided. It is shown that traditional methods remain technologically robust but are limited in their capabilities for miniaturization and interfacial architecture design. Modern thin-film and additive approaches provide high spatial accuracy, improved ion-electron characteristics, and flexibility in the design of multilayer structures; however, they require addressing issues related to scalability, ink stability, interfacial compatibility, and reproducibility. Particular attention is paid to interfacial engineering methods, such as functionally graded layers, nanostructured infiltration, and temperature-controlled 3D printing. Key challenges are discussed, including thermal instability of materials, the limited gas impermeability of ultra-thin electrolytes, and degradation during long-term operation. Development prospects lie in the integration of hybrid methods, the digitalization of deposition processes, and the implementation of intelligent control of printing parameters. The presented analysis forms the basis for further research into the scalable and highly efficient production of next-generation SOFCs designed for low-temperature operation and long-term operation in future energy systems. Full article

With the advancement of Internet of Things (IoT) technology, flexible sensors with dual optoelectronic sensing modes have emerged as a research hotspot for next-generation smart devices, further driving the urgent demand for environmentally friendly functional materials. Here, we innovatively integrated wastepaper recycling technology with a polyethyleneimine (PEI)-assisted pulping strategy to develop a novel cellulose-based sustainable photo-triboelectric hybrid nanogenerator (PT-HNG). Based on the working mechanism of a freestanding triboelectric nanogenerator (TENG), the PT-HNG can directly convert pressure stimuli into electrical energy and triboelectrification-induced electroluminescence (TIEL) signals. It achieves luminescence brightness of 0.06 mW cm⁻² (3.84 cd m⁻²) and simultaneously delivers excellent electrical output performance (172.4 V, 6.36 μA, 43.7 nC) under sliding motion. More importantly, compatible with existing industrial papermaking processes, the PT-HNG is scalable for large-scale production. By combining PT-HNG with deep learning algorithms, a handwritten e-book system based on trajectory recognition was constructed, with a recognition accuracy of up to 95.5%. In addition, real-time intelligent control of PowerPoint presentations via PT-HNG was demonstrated. This study provides a new pathway for converting wastepaper into intelligent products and presents a novel idea for the interdisciplinary integration of the circular economy and advanced electronic technology. Full article