Pr/Yb doped materials have been widely reported as quantum-cutting materials in recent times. However, the question of the energy transfer mechanism in the Pr/Yb pair in light of the quantum-cutting phenomenon still remains unanswered. In view of that, we explored a series of Pr/Yb co-doped low phonon fluorotellurite glass systems to estimate the probability of different energy transfer mechanisms. Indeed, a novel and simple way to predict the probability of the proper energy transfer mechanism in the Pr/Yb pair is possible by considering the donor Pr ion emission intensities and the relative ratio dependence in the presence of acceptor Yb ions. Moreover, the observed results are very much in accordance with other estimated results that support the quantum-cutting phenomena in Pr/Yb pairs, such as sub-linear power dependence of Yb NIR emission upon visible ∼450 nm laser excitation, integrated area of the donor Pr ion's visible excitation spectrum recorded by monitoring the acceptor Yb ion's NIR emission, and the experimentally obtained absolute quantum yield values using an integrating sphere setup. Our results give a simple way of estimating the probability of an energy transfer mechanism and the factors to be considered, particularly for the Pr/Yb pair.
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March 2025
Department of Applied Chemistry, Petroleum and Chemical Industry Key Laboratory of Organic Electrochemical Synthesis, State Key Laboratory of Green Chemistry Synthesis Technology, Zhejiang University of Technology, Hangzhou, 310014, P. R. China.
Electrocatalytic hydrogenation (ECH) of quinoline provides an eco-friendly and prospective route to achieve the highly value-added generation of 1,2,3,4-tetrahydroquinoline (THQ). Co element has been proven to be the efficient catalytic site for ECH of quinoline, but the rational regulation of the electronic structure of active Co site to improve the activity is still a challenge. Herein, the hierarchical core-shell structure consisting of NiCo-MOF nanosheets encapsulated Cu(OH) nanorods (Cu(OH)@CoNi-MOF) is constructed.
View Article and Find Full Text PDFSmall
March 2025
College of Materials Science and Engineering, Fuzhou University, Fuzhou, 350108, China.
The sluggish reaction kinetics and formidable shuttle effect of soluble lithium polysulfides (LiPSs) are thorny problems for the future industrialization of lithium-sulfur (Li-S) batteries. Therefore, exploring efficient electrocatalysts to capture LiPSs and accelerate their conversion is highly desirable yet tremendously challenging. Herein, a high-efficiency Bi/BiO/VMoN@rGO electrocatalyst with multifunctional active sites and multilevel heterointerfaces is elaborately designed for Li-S batteries.
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March 2025
College of Materials Science and Engineering, Fuzhou University, New Campus, Minhou, Fujian, 350108, China.
Overcoming the challenges of integrating disparate components in nanoarchitectures, this study introduces a straightforward strategy based on a mixed-valence coordination approach, creating an ordered ternary heterostructure integrated with ultrasmall homojunction. This singular ordered homojunction-heterostructure unites ultrathin 1D rutile TiO nanowires (NWs) and ultrathin anatase TiO NWs with 0D Prussian Blue Analogs (PBAs) nanoparticles (NPs), all exhibiting crystallographic oriented alignment with each other, forming a ternary mesocrystals. Experimental and theoretical insights disclose that the complex interplay between these dissimilar components is governed by a spontaneous lattice match effect, which not only optimizes but also directs the charge transfer, thereby enhancing both efficiency and stability.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
March 2025
Central South University, School of Metallurgy and Enviroment, No. 932, Lushan Road,, Changsha city, Hunan Province, 410083, Changsha, CHINA.
Activated by the Li-O-Li configuration with nonbonding O2p state (lO2p), anionic redox reaction (ARR) in Li-rich layered oxides (LLOs) contributes to additional capacity but exhibits significant irreversibility, leading to severe surface oxygen loss. Herein, surface nonbonding oxygen state (SNBOS) is regulated by the integrated surface structure engineering to suppress surface oxygen loss and enhance the reversibility of ARR. On the outermost layer, the conversion of layered structure into a LiLaO2 layer and spinel phase structure eliminates lO2p, thereby preventing the activation of ARR and suppressing side reaction between electrolyte and oxidized oxygen ions.
View Article and Find Full Text PDFInorg Chem
March 2025
College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, PR China.
Integrating mixed electron donor (D) and electron acceptor (A) ligands into metal-organic frameworks (MOFs) is an effective yet relatively unexplored approach for improving the anode performance of hybrid lithium-ion capacitors (HLICs). In this study, using an electron donor 2,6-bis(4'-pyridyl)tetrathiafulvalene and an electron acceptor ,'-bis(5-isophthalic acid) naphthalene diimide as ligands, a new Zn-TTF/NDI MOF () is constructed as a pseudocapacitive anode of HLICs. Crystallographic characterization revealed that MOF adopts a two-dimensional (2D) coordination network.
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