Gases evolved from lithium batteries can drastically affect their performance and safety; for example, cell swelling is a serious safety issue. Here, we combine operando pressure measurements and online electrochemical mass spectrometry measurements to identify the nature and quantity of gases formed in batteries with graphite and lithium metal electrodes. We demonstrate that ethylene, a main gas evolved in SEI formation reactions, is quickly consumed at lithium metal electrodes unless they have been pretreated in the electrolyte. Polyolefins such as polyethylene are suggested as the possible reaction product from ethylene consumption, evidencing another pathway of SEI formation that had been previously overlooked because it does not produce any gas product.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11331504PMC
http://dx.doi.org/10.1021/acs.jpcc.4c03656DOI Listing

Publication Analysis

Top Keywords

lithium metal
12
graphite lithium
8
metal electrodes
8
sei formation
8
differences interfacial
4
interfacial reactivity
4
reactivity graphite
4
lithium
4
metal battery
4
battery electrodes
4

Similar Publications

The recycling of spent lithium-ion batteries has become a common concern of the whole society, with a large number of studies on recycling management and recycling technology, but there is relatively little study on the pollution release during the recycling process. Pollution will restrict the healthy development of the recycling industry, which makes relevant research very significant. This paper monitored and analyzed the battery recycling pretreatment process in a formal factory, and studied the pollution characteristics of particulate matter, heavy metals, and microplastics under different treatment stages.

View Article and Find Full Text PDF

Lithium-tellurium (Li-Te) batteries are gaining attention as a promising next-generation energy storage system due to their superior electrical conductivity and high volumetric capacity compared to sulfur and selenium. Tellurium's unique properties, such as suitable redox potential, excellent conductivity, high volumetric capacity, and greatest stability, position it as a strong candidate for negative electrode materials. This study explores the potential of metal tellurides, specifically CuTe and FeTe monolayers, as effective tellurium host materials, leveraging their polar interactions with lithium polytellurides.

View Article and Find Full Text PDF

Developing high-energy-density lithium-sulfur batteries faces serious polysulfide shuttle effects and sluggish conversion kinetics, often necessitating the excessive use of electrolytes, which in turn adversely affects battery performance. Our study introduces a meticulously designed electrocatalyst, Cu-CeO@N/C, to enhance lean-electrolyte lithium-sulfur battery performance. This catalyst, featuring in situ synthesized Cu clusters, regulates oxygen vacancies in CeO and forms Cu-CeO heterojunctions, thereby diminishing sulfur conversion barriers and hastening reaction kinetics through the generation of S/S intermediates.

View Article and Find Full Text PDF

Regulating Lithium-Ion Transport in PEO-Based Solid-State Electrolytes through Microstructures of Clay Minerals.

ACS Appl Mater Interfaces

January 2025

Research Center of Resource Chemistry and Energy Materials, Key Laboratory of Clay Mineral of Gansu, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, Lanzhou 730000, P.R. China.

Clay minerals show significant potential as fillers in polymer composite solid electrolytes (CSEs), whereas the influence of their microstructures on lithium-ion (Li) transport properties remains insufficiently understood. Herein, we design advanced poly(ethylene oxide) (PEO)-based CSEs incorporating clay minerals with diverse microstructures including 1D halloysite nanotubes, 2D Laponite (Lap) nanosheets, and 3D porous diatomite. These minerals form distinct Li transport pathways at the clay-PEO interfaces due to their varied structural configurations.

View Article and Find Full Text PDF

Biomimetic calcification is a micro-crystallization process that mimics the natural biomineralization process, where biomacromolecules regulate the formation of inorganic minerals. In this study, it is presented that a protein-assisted biomimetic calcification method for the in situ synthesis of nitrogen-doped metal-organic framework (MOF) materials. A series of unique core-shell structures are created by utilizing proteins as templates and guiding agents in the nucleation step, creating ideal conditions for shell growth.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!