Results 41 to 50 of about 232,746 (342)

Receptor‐Free Identification of Toxic Gases Enabled by Hygroscopic Aqueous Salt Films

open access: yesAdvanced Functional Materials, EarlyView.
Water as a gas sensor coating sounds impossible—until it stops evaporating. Here, hygroscopic salt solutions (LiCl, LiBr, H3PO4) form non‐drying aqueous films on CNT chemiresistors under ambient air. Gases partition into these liquid layers, sometimes transforming into water, and generate salt‐specific resistance fingerprints across a four‐channel ...
Seongwoo Lee   +5 more
wiley   +1 more source

Poly(amic acid) Lithium Salt as a Multi-Functional Binder for High Performance Lithium/Sulfur Battery Cathodes

open access: yesInternational Journal of Electrochemical Science, 2019
Water-soluble poly(amic acid) lithium (PAALi) salts were firstly used as the binders for lithium/sulfur battery. Benefiting plenty functional groups (amide and carboxylate), S@PAALi cathodes with sulfur loading of ca.
Guomin Zhao   +3 more
doaj   +1 more source

Solid state lithiation-delithiation of sulphur in sub-nano confinement: a new concept for designing lithium-sulphur batteries. [PDF]

open access: yes, 2016
We investigate the detailed effects and mechanisms of sub-nano confinement on lithium-sulfur (Li-S) electrochemical reactions in both ether-based and carbonate-based electrolytes.
Bozhilov, Krassimir N   +3 more
core   +1 more source

Electrolyte Design Strategies for Static Shuttle‐Free and Long‐Life Aqueous Zinc‐Iodine Batteries

open access: yesAdvanced Functional Materials, EarlyView.
This review systematically summarizes recent advances in electrolyte design for static aqueous Zn‐I2 batteries, highlighting solvation regulation and interfacial engineering strategies to control reaction kinetics, suppress iodine shuttling, enhance energy density, and stabilize multi‐electron iodine redox chemistry for durable, high‐performance energy
Qianqin Zhou   +3 more
wiley   +1 more source

Kinetic activation of interfacial Li2S via zirconia membrane reactor confinement catalysis for high‐performance lithium/sulfur batteries

open access: yesInfoMat
The slow kinetics and irreversibility of Li2S deposition and dissolution during the sulfur reduction/evolution reactions (SRR/SER) hinder the fast‐charging and high‐rate capabilities of lithium–sulfur (Li/S) batteries.
Lei Ji   +9 more
doaj   +1 more source

Plane Double-Layer Structure of AC@S Cathode Improves Electrochemical Performance for Lithium-Sulfur Battery

open access: yesFrontiers in Chemistry, 2018
Due to the high theoretical specific capacity of lithium-sulfur batteries, it is considered the most promising electrochemical energy storage device for the next generation.
Zengren Tao   +5 more
doaj   +1 more source

Rubber-Derived Sulfur Composite Cathode Material for Li-S/Li-ion Battery

open access: yesElectrochemistry, 2022
A rubber-derived sulfur composite cathode material for the Li-S battery/Li-ion battery was synthesized by the vulcanization process of butadiene rubber as a polymer source and a large amount of sulfur.
Akihiro YAMANO   +11 more
doaj   +1 more source

Single‐ and Dual‐Atom Configurations in Atomically Dispersed Catalysts for Lithium–Sulfur Batteries

open access: yesAdvanced Functional Materials, EarlyView.
Single‐atom and dual‐atom‐based atomically dispersed catalysts (ADCs) effectively address the shuttle effect and sluggish redox kinetics in Li–S batteries. With nearly 100% atomic utilization and tunable coordination environments, ADCs enhance LiPSs adsorption, lower conversion barriers, and accelerate sulfur redox reactions.
Haoyang Xu   +4 more
wiley   +1 more source

Nanofiber‐Confined 2H‐NbSe2 With a Li2S Activation Interface for 10 C Fast‐Charging Lithium–Sulfur Batteries

open access: yesEcoEnergy
The uncontrolled shuttle of lithium polysulfides (LiPSs) and sluggish Li2S conversion kinetics critically limits the high‐rate performance of lithium–sulfur (Li–S) batteries.
Jiayi Xue   +9 more
doaj   +1 more source

Establishing a Model Precursor System: Over a Decade of Research on Carbon Dots from the Citric Acid‐Urea System

open access: yesAdvanced Functional Materials, EarlyView.
The citric acid/urea (CA‐Urea) precursor system offers a versatile, scalable route to carbon dots with tunable luminescence and multifunctionality. Mechanistic insights into precursor chemistry and reaction parameters have enabled doping, surface modification, and hybridization strategies, yielding CDs for luminescent devices, sensing, catalysis ...
Yupeng Liu   +10 more
wiley   +1 more source

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