TY - JOUR
T1 - Quantitative Neutralization of Polyacrylic Acid Binders for Lithium-Ion Pouch Cells with a Coulombic Efficiency Exceeding 99.9%
AU - Mo, Haoran
AU - Wang, Cuie
AU - Shen, Hui
AU - Ran, Ran
AU - Zhou, Wei
AU - Liao, Kaiming
N1 - Publisher Copyright:
© 2025 American Chemical Society.
PY - 2025
Y1 - 2025
N2 - The binder plays a critical role in lithium-ion batteries by promoting the cohesion of active material particles and ensuring their stable adhesion to the current collector. Poly(acrylic acid) (PAA), a water-soluble polymer, has garnered considerable interest as a binder in numerous applications, particularly in energy storage systems, such as batteries and supercapacitors. However, the self-association of the carboxyl (−COOH) functional groups in PAA results in the formation of both intramolecular and intermolecular hydrogen bonds, which significantly compromises the adhesive’s binding strength to the current collector surface. Herein, we introduce a quantitatively neutralized poly(acrylic acid) (QN-PAA) binder designed to optimize interfacial adhesion strength and mechanical integrity. This binder promotes an in situ reaction between −COOH groups in PAA and copper oxide (CuO) layers on the surface of a copper foil current collector under thermally regulated conditions. The reaction forms durable ionic cross-linked networks (−COO-···Cu2+···-OOC−) that stabilize the active material-current collector interface while enhancing electrochemical compatibility. As a result, electrodes fabricated with 3 wt % QN-PAA-bonded graphite on a copper-current collector exhibit exceptional durability, sustaining over 30,000 consecutive bending cycles without structural disintegration or active material delamination. Notably, lithium-ion pouch cells (1 Ah) assembled with the QN-PAA binder exhibited a capacity retention rate of about 100% and Coulombic efficiency exceeding 99.9% over 100 cycles.
AB - The binder plays a critical role in lithium-ion batteries by promoting the cohesion of active material particles and ensuring their stable adhesion to the current collector. Poly(acrylic acid) (PAA), a water-soluble polymer, has garnered considerable interest as a binder in numerous applications, particularly in energy storage systems, such as batteries and supercapacitors. However, the self-association of the carboxyl (−COOH) functional groups in PAA results in the formation of both intramolecular and intermolecular hydrogen bonds, which significantly compromises the adhesive’s binding strength to the current collector surface. Herein, we introduce a quantitatively neutralized poly(acrylic acid) (QN-PAA) binder designed to optimize interfacial adhesion strength and mechanical integrity. This binder promotes an in situ reaction between −COOH groups in PAA and copper oxide (CuO) layers on the surface of a copper foil current collector under thermally regulated conditions. The reaction forms durable ionic cross-linked networks (−COO-···Cu2+···-OOC−) that stabilize the active material-current collector interface while enhancing electrochemical compatibility. As a result, electrodes fabricated with 3 wt % QN-PAA-bonded graphite on a copper-current collector exhibit exceptional durability, sustaining over 30,000 consecutive bending cycles without structural disintegration or active material delamination. Notably, lithium-ion pouch cells (1 Ah) assembled with the QN-PAA binder exhibited a capacity retention rate of about 100% and Coulombic efficiency exceeding 99.9% over 100 cycles.
UR - http://www.scopus.com/inward/record.url?scp=105006730021&partnerID=8YFLogxK
U2 - 10.1021/acs.energyfuels.5c02019
DO - 10.1021/acs.energyfuels.5c02019
M3 - 文章
AN - SCOPUS:105006730021
SN - 0887-0624
JO - Energy and Fuels
JF - Energy and Fuels
ER -