Publications by authors named "Yuansen Xie"

Electrocatalysis is generally confined to dynamic liquid-solid and gas-solid interfaces and is rarely applicable in solid-state reactions. Here, we report a paradigm shift strategy to exploit electrocatalysis to accelerate solid-state reactions in the context of lithium-ion batteries (LIBs). We employ heteroatom doping, specifically boron for silicon and sulfur for phosphorus, to catalyze electrochemical Li-alloying reactions in solid-state electrode materials.

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Li de-solvation at solid-electrolyte interphase (SEI)-electrolyte interface stands as a pivotal step that imposes limitations on the fast-charging capability and low-temperature performance of lithium-ion batteries (LIBs). Unraveling the contributions of key constituents in the SEI that facilitate Li de-solvation and deciphering their mechanisms, as a design principle for the interfacial structure of anode materials, is still a challenge. Herein, we conducted a systematic exploration of the influence exerted by various inorganic components (LiCO, LiF, LiPO) found in the SEI on their role in promoting the Li de-solvation.

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Article Synopsis
  • Alloy anode materials are being researched for potassium storage because they have a high theoretical capacity, but they struggle with structural strain and fragmentation when deeply charged with potassium.
  • This study introduces a strategy that involves modifying the chemical bonds in these materials to better handle the volume changes during the charging process, specifically using black phosphorus with added sulfur.
  • The result is a more stable anode that supports higher capacity and longer lifespan for potassium-ion batteries, indicating progress in balancing the challenges of low-strain and effective charging.
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Article Synopsis
  • Lithium-ion batteries (LIBs) using ethylene carbonate electrolytes and graphite anodes face energy loss at low temperatures due to electrolyte viscosity and slow lithium transportation.
  • A lithium phosphide (LiP) coating on the graphite improves ion conductivity and accelerates lithium movement, effectively addressing these issues.
  • This innovation allows LIBs to retain 70% of their room-temperature capacity at -20 °C and maintain 65% at -40 °C, significantly enhancing performance in cold environments.
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Electrochemical Li-alloying reactions with Li-rich alloy phases render a much higher theoretical capacity that is critical for high-energy batteries, and the accompanying phase transition determines the alloying/dealloying reversibility and cycling stability. However, the influence of phase-transition characteristics upon the thermodynamic properties and diffusion kinetic mechanisms among the two categories of alloys, solid-solutions and intermetallic compounds, remains incomplete. Here we investigated three representative Li-alloys: Li-Ag alloy of extended solid-solution regions; Li-Zn alloy of an intermetallic compound with a solid-solution phase of a very narrow window in Li atom concentration; and Li-Al alloy of an intermetallic compound.

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In view of their high lithium storage capability, phosphorus-based anodes are promising for lithium-ion batteries. However, the low reduction potential (0.74 V versus Li /Li) of the commonly used ethylene carbonate-based electrolyte does not allow the early formation of a solid electrolyte interphase (SEI) prior to the initial phosphorus alloying reaction (1.

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