Self-assembled materials with complex nanoscale and mesoscale architecture attract considerable attention in energy and sustainability technologies. Their high performance can be attributed to high surface area, quantum effects, and hierarchical organization. Delineation of these contributions is, however, difficult because complex materials display stochastic structural patterns combining both order and disorder, which is difficult to be consistently reproduced yet being important for materials' functionality. Their compositional variability make systematic studies even harder. Here, a model system of FeSe "hedgehog" particles (HPs) was selected to gain insight into the mechanisms of charge storage n complex nanostructured materials common for batteries and supercapacitors. Specifically, HPs represent self-assembled biomimetic nanomaterials with a medium level of complexity; they display an organizational pattern of spiky colloids with considerable disorder yet non-random; this patternt is consistently reproduced from particle to particle. . It was found that HPs can accommodate ≈70× greater charge density than spheroidal nano- and microparticles. Besides expanded surface area, the enhanced charge storage capacity was enabled by improved hole transport and reversible atomic conformations of FeSe layers in the blade-like spikes associated with the rotatory motion of the Se atoms around Fe center. The dispersibility of HPs also enables their easy integration into energy storage devices. HPs quadruple stored electrochemical energy and double the storage modulus of structural supercapacitors.
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http://dx.doi.org/10.1002/advs.202305085 | DOI Listing |
Molecular junctions (MJs) are celebrated nanoelectronic devices for mimicking conventional electronic functions, including rectifiers, sensors, wires, switches, transistors, negative differential resistance, and memory, following an understanding of charge transport mechanisms. However, capacitive nanoscale molecular junctions are rarely seen. The present work describes electrochemically (E-Chem) grown covalently attached molecular thin films of 10, 14.
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January 2025
Plasmonic Nanomaterials Laboratory, Department of Nanoscience and Technology, PSG Institute of Advanced Studies Peelamedu Coimbatore-641 004 Tamilnadu India
Escalating energy demands have often ignited ground-breaking innovations in the current era of electrochemical energy storage systems. Supercapacitors (SCs) have emerged as frontrunners in this regard owing to their exclusive features such ultra-high cyclic stability, power density, and ability to be derived from sustainable sources. Despite their promising attributes, they typically fail in terms of energy density, which poses a significant hindrance to their widespread commercialization.
View Article and Find Full Text PDFNanoscale Horiz
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Laboratory of Advanced Materials, Shanghai Key Lab of Molecular Catalysis and Innovative Materials, Academy for Engineering & Technology, Advanced Coatings Research Center of Ministry of Education of China, Fudan University, Shanghai 200438, P. R. China.
A porous hedgehog-like CoO/NiO/graphene oxide (denoted as PHCNO/GO) microsphere was prepared by a facile solvothermal method, followed by an annealing treatment under argon atmosphere. Benefiting from the thin CoO/NiO nanosheets with a large specific surface area, abundant pores distributed between the CoO/NiO nanosheets, and GO firmly wrapped around the surface of PHCNO microspheres, the PHCNO/GO microspheres showed excellent lithium storage performance. The CoO/NiO nanosheets provided numerous active sites, achieving a high reversible specific capacity.
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School of Chemistry and Materials Science, Hangzhou Institute for Advanced Study University of Chinese Academy of Sciences, Hangzhou, 310024, P. R. China.
Metal-free photocatalysts derived from earth-abundant elements have drawn significant attention owing to their ample supply for potential large-scale applications. However, it is still challenging to achieve highly efficient photocatalytic performance owing to their sluggish charge separation and lack of active catalytic sites. Herein, we designed and constructed a series of covalently bonded organic semiconductors to enhance water splitting and phenol degradation.
View Article and Find Full Text PDFAdv Mater
January 2025
Key Laboratory of Power Station Energy Transfer Conversion and System of Ministry of Education and School of Energy Power and Mechanical Engineering, and Beijing Laboratory of New Energy Storage Technology, North China Electric Power University, Beijing, 102206, China.
Co-free high-Ni layered cathode materials LiNiMeO (Me = Mn, Mg, Al, etc.) are a key part of the next-generation high-energy lithium-ion batteries (LIBs) due to their high specific capacity and low cost. However, the hindered Li kinetics and the high reactivity of Ni result in poor rate performance and unsatisfied cycling stability.
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