Passive Self-Homogenization in Series-Connected Battery Packs: A Structural Theorem, a First-Order Saturation Law, and Linearized Stability

Problem. Cell-to-cell internal-resistance dispersion is amplified at sub-zero temperatures and is widely regarded as the root cause of pack-level capacity loss and lifetime divergence. Countermeasures converge on one idea: eliminate the dispersion—active balancing, external preheating, and stringent dual-parameter sorting (capacity and resistance). A reversed proposition has been largely overlooked: in a series string, where current is common, resistance dispersion itself drives a passive self-homogenization mechanismthe highest-resistance cell dissipates the most Joule heat, warms the most, and its resistance drops the most, so it “catches up” with its lower-resistance neighbours. Challenge. All existing evidence for this mechanism is phenomenological simulation. Three fundamental questions lack analytical answers: Is the observed compression a physical necessity or a parameter coincidence? How large is it, and is there a simple scaling law? Does it converge in a real pack with inter-cell thermal diffusion? Contributions. Under three explicit assumptions we establish: (i) a self-homogenization theorem—the operating relative resistance dispersion is compressed by 1/(1+Λ) ∈ (0,1], whose sign is locked solely by 𝜕R/𝜕T<0 and is therefore independent of parameter values and implementation; (ii) a first-order saturation law flat% = Λ/(1+Λ)—exact in the pure-resistance channel (zero capacity dispersion), predicting the equalization magnitude from the single parameter Λ = 𝛽ꞏΔT̄ (15.2% predicted vs 16.2% simulated at the baseline cell, Δ = 1.0 pp), together with a two-channel superposition formula for the general case and an honest disclosure of the quantitative gap between the first-order estimate and simulation (8.6% vs 16.2%, attributed to the convexity of the cut-off map); (iii) asymptotic stability within the linearized modelwith inter-cell thermal diffusion the coupled thermo-electric ODE has a diagonally dominant Jacobian with all-negative eigenvalues, so self-equalization is an eigenstate of the linear system. The theory further yields an analytic left-boundary criterion for the operating sweet spot (ΔT̄≥ 0.176/𝛽) and explains why sodium-ion cells are the largest beneficiaries.

Authors

Publication Details

Journal
ChemRxiv
Published
2026-10-27
DOI
https://doi.org/10.26434/chemrxiv.15011110/v1
Primary Topic
Advanced Battery Technologies Research
Type
preprint
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
preprint

Passive Self-Homogenization in Series-Connected Battery Packs: A Structural Theorem, a First-Order Saturation Law, and Linearized Stability

Bo Yang, 杨博 杨
4 links
ChemRxiv
Advanced Battery Technologies Research
preprint

Passive Self-Homogenization in Series-Connected Battery Packs: A Structural Theorem, a First-Order Saturation Law, and Linearized Stability

Bo Yang, 杨博 杨
preprint en

Abstract

Problem. Cell-to-cell internal-resistance dispersion is amplified at sub-zero temperatures and is widely regarded as the root cause of pack-level capacity loss and lifetime divergence. Countermeasures converge on one idea: eliminate the dispersion—active balancing, external preheating, and stringent dual-parameter sorting (capacity and resistance). A reversed proposition has been largely overlooked: in a series string, where current is common, resistance dispersion itself drives a passive self-homogenization mechanismthe highest-resistance cell dissipates the most Joule heat, warms the most, and its resistance drops the most, so it “catches up” with its lower-resistance neighbours. Challenge. All existing evidence for this mechanism is phenomenological simulation. Three fundamental questions lack analytical answers: Is the observed compression a physical necessity or a parameter coincidence? How large is it, and is there a simple scaling law? Does it converge in a real pack with inter-cell thermal diffusion? Contributions. Under three explicit assumptions we establish: (i) a self-homogenization theorem—the operating relative resistance dispersion is compressed by 1/(1+Λ) ∈ (0,1], whose sign is locked solely by 𝜕R/𝜕T<0 and is therefore independent of parameter values and implementation; (ii) a first-order saturation law flat% = Λ/(1+Λ)—exact in the pure-resistance channel (zero capacity dispersion), predicting the equalization magnitude from the single parameter Λ = 𝛽ꞏΔT̄ (15.2% predicted vs 16.2% simulated at the baseline cell, Δ = 1.0 pp), together with a two-channel superposition formula for the general case and an honest disclosure of the quantitative gap between the first-order estimate and simulation (8.6% vs 16.2%, attributed to the convexity of the cut-off map); (iii) asymptotic stability within the linearized modelwith inter-cell thermal diffusion the coupled thermo-electric ODE has a diagonally dominant Jacobian with all-negative eigenvalues, so self-equalization is an eigenstate of the linear system. The theory further yields an analytic left-boundary criterion for the operating sweet spot (ΔT̄≥ 0.176/𝛽) and explains why sodium-ion cells are the largest beneficiaries.

ChemRxiv
Affordable and clean energy
Advanced Battery Technologies Research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Laika access coming soon
Passive Self-Homogenization in Series-Connected Battery Packs: A Structural Theorem, a First-Order Saturation Law, and Linearized Stability — Bo Yang, 杨博 杨 · ChemRxiv (2026) | TGRS Research Map | TGRS