Publications by authors named "Sijiang Hu"

Lithium metal batteries (LMBs) employing high-voltage cathode present a promising pathway toward high-energy-density energy storage systems. However, critical challenges have hindered their practical application, including lithium dendrite proliferation, unstable solid-electrolyte interphase (SEI), and limited oxidative stability of conventional 1,2-dimethoxyethane (DME)-based electrolytes. Herein, we rationally design a siloxane-based electrolyte system featuring enhanced oxidative stability through solvent molecular engineering.

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Inhomogeneous lithium (Li) deposition and unstable solid electrolyte interphase are the main causes of short cycle life and safety issues in Li metal batteries (LMBs). Developing a 3D structured matrix current collector and novel electrolyte are feasible strategies to tackle these issues. Ether-based electrolytes are widely used in LMBs.

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Lithium metal batteries (LMBs) promise high-energy-density storage but face safety issues due to dendrite-induced lithium deposition, irreversible electrolyte consumption, and large volume changes, which hinder their practical applications. To address these issues, tuning lithium deposition by structuring a host for the lithium metal anode has been recognized as an efficient method. Herein, we report a supercritical water molecular scissor-controlled strategy to form a carbon framework derived from biomass wood.

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Cobalt sulfide (CoS) is a promising anode material for sodium-ion batteries (SIBs) due to its high theoretical capacity, cost-effectiveness, and environmental friendliness. Unfortunately, the inevitable structural deterioration induced by the huge volume changes during the discharge/charge cycles leads to poor cycle performance and rate capability when evaluated as the anode material for SIB. Herein, we designed a CoS@C-MoS heterostructure with abundant heterointerface and hollow structure.

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Iron sulfides have shown great potential as anode materials for sodium-ion batteries (SIBs) because of their high sodium storage capacity and low cost. Nevertheless, iron sulfides generally exhibit unsatisfied electrochemical performance induced by sluggish electron/ion transfer and severe pulverization upon the sodiation/desodiation process. Herein, we constructed a yolk-shell FeS@NC nanosphere with an N-doped carbon shell and FeS particle core via a simple hydrothermal method, followed by in-situ polymerization and vulcanization.

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P2-NaNiMnO cathode materials have garnered significant attention due to their high cationic and anionic redox capacity under high voltage. However, the challenge of structural instability caused by lattice oxygen evolution and P2-O2 phase transition during deep charging persists. A breakthrough is achieved through a simple one-step synthesis of Cr, Mg co-doped P2-NaNMCM, resulting in a bi-functional improvement effect.

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Li-rich layered oxides have attracted intense attention for lithium-ion batteries, as provide substantial capacity from transition metal cation redox simultaneous with reversible oxygen-anion redox. However, unregulated irreversible oxygen-anion redox leads to critical issues such as voltage fade and oxygen release. Here, we report a feasible NiFeO (NFO) surface-coating strategy to turn the nonbonding coordination of surface oxygen into metal-oxygen decoordination.

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The oxygen evolution reaction (OER) is an important reaction especially in water splitting and metal-air batteries. Highly efficient non-noble metal based electrocatalysts are urgently required to be developed and to replace the commercial Ru/Ir based oxide. Herein, we report the three-dimensional hierarchical NiCoO/CNT-150 composite with high activity for the OER that was synthesized a hydrothermal reaction and subsequent annealing.

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A three dimensional (3D) Al2O3 coating layer was synthesized by a facile approach including stripping and in situ self-assembly of γ-AlOOH. The uniform flower-like Al2O3 nanosheets with high specific area largely sequesters acidic species produced by side reaction between electrode and electrolyte. The inner coating layer wrapping spinel LiMn2O4 effectively inhibits the dissolution of Mn by suppressing directive contact with electrolyte to enhance cycling stability.

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