The Five Key Causes of Lithium Iron Phosphate Battery Degradation and Four Key Remedial Measures


Continuous consumption of active lithium ions
During the cycling process of the battery, the solid electrolyte interface (SEI) film on the negative electrode surface will undergo micro cracking due to charge and discharge stress, requiring the consumption of active lithium ions for repair. Especially in the first 50 cycles, the expansion rate of the polarizer can reach 3.3%, leading to frequent rupture of the SEI film and rapid capacity decay in the early stages. This process is irreversible and directly reduces the total amount of lithium ions that can participate in the reaction.


Inconsistencies between battery cells cause chain decay
A battery pack is composed of multiple individual cells connected in series. If the capacity or internal resistance of individual cells is too high, it will cause drastic changes in the overall voltage, and some cells will be in an overcharge or overdischarge state for a long time, accelerating their aging and affecting the overall performance of the pack. This "barrel effect" is particularly prominent in the fast charging scenario of commercial vehicles.


High temperature and fast charging accelerate side reactions
High temperature (>45 ℃) will accelerate electrolyte decomposition and SEI film thickening, leading to an increase in internal resistance; High power fast charging generates a large amount of heat, further exacerbating material degradation. Experiments have shown that storing at 60 ℃ for 30 days can result in a capacity loss of up to 15%. Commercial vehicles have significantly shortened battery life due to high time costs and long-term reliance on fast charging.


Ion diffusion is hindered in low-temperature environments
The olivine structure of lithium iron phosphate is a one-dimensional lithium-ion channel, and the ion migration rate decreases significantly at low temperatures. The discharge capacity may decay to below 50% of room temperature at -10 ℃. Meanwhile, BMS is difficult to accurately estimate SOC, which can easily lead to the phenomenon of "virtual electricity".


Improper usage habits amplify the risk of attenuation
Long term shallow charging and discharging (such as only charging to 80%) can lead to inaccurate BMS power calibration, resulting in issues such as falsely high battery life displayed on the meter and fast actual power failure. Research shows that the three-year decay rate of lithium iron phosphate batteries with long-term shallow charging and discharging can reach 35%, much higher than the 18% calibrated with regular full charging. In addition, long-term storage at a loss of electricity (<20%) can cause lithium dendrite precipitation, posing a threat to safety.

Four major improvement measures to delay attenuation

Scientific Charging Strategy: Regular Full Charge Calibration to Avoid Deep Discharge
It is recommended to perform a slow full charge once a week to help BMS accurately calibrate SOC and prevent battery imbalance. During daily use, discharge not less than 20% to avoid lithium deposition on the negative electrode. When parked for a long time, maintain the battery level at 50% -70% and stay away from high temperature and humid environments.


Reduce fast charging frequency and prioritize using slow charging
Although fast charging is convenient, high current can exacerbate electrolyte aging and thermal stress. It is recommended to use fast charging as an emergency measure and slow charging as much as possible for daily energy replenishment to extend battery life.


Optimize thermal management and BMS algorithm
Adopting a liquid cooling+active heating system to ensure that the battery operates within the optimal temperature range of 0-20 ℃. BMS should have dynamic balancing function, adjust the voltage of each battery cell in real time, and prevent individual battery cells from overloading. Ningde Times Shenxing Battery has been optimized through the synergy of high voltage density and low viscosity electrolyte to enhance low-temperature performance.

Continuous consumption of active lithium ions
During the cycling process of the battery, the solid electrolyte interface (SEI) film on the negative electrode surface will undergo micro cracking due to charge and discharge stress, requiring the consumption of active lithium ions for repair. Especially in the first 50 cycles, the expansion rate of the polarizer can reach 3.3%, leading to frequent rupture of the SEI film and rapid capacity decay in the early stages. This process is irreversible and directly reduces the total amount of lithium ions that can participate in the reaction.


Inconsistencies between battery cells cause chain decay
A battery pack is composed of multiple individual cells connected in series. If the capacity or internal resistance of individual cells is too high, it will cause drastic changes in the overall voltage, and some cells will be in an overcharge or overdischarge state for a long time, accelerating their aging and affecting the overall performance of the pack. This "barrel effect" is particularly prominent in the fast charging scenario of commercial vehicles.


High temperature and fast charging accelerate side reactions
High temperature (>45 ℃) will accelerate electrolyte decomposition and SEI film thickening, leading to an increase in internal resistance; High power fast charging generates a large amount of heat, further exacerbating material degradation. Experiments have shown that storing at 60 ℃ for 30 days can result in a capacity loss of up to 15%. Commercial vehicles have significantly shortened battery life due to high time costs and long-term reliance on fast charging.


Ion diffusion is hindered in low-temperature environments
The olivine structure of lithium iron phosphate is a one-dimensional lithium-ion channel, and the ion migration rate decreases significantly at low temperatures. The discharge capacity may decay to below 50% of room temperature at -10 ℃. Meanwhile, BMS is difficult to accurately estimate SOC, which can easily lead to the phenomenon of "virtual electricity".


Improper usage habits amplify the risk of attenuation
Long term shallow charging and discharging (such as only charging to 80%) can lead to inaccurate BMS power calibration, resulting in issues such as falsely high battery life displayed on the meter and fast actual power failure. Research shows that the three-year decay rate of lithium iron phosphate batteries with long-term shallow charging and discharging can reach 35%, much higher than the 18% calibrated with regular full charging. In addition, long-term storage at a loss of electricity (<20%) can cause lithium dendrite precipitation, posing a threat to safety.

Four major improvement measures to delay attenuation

Scientific Charging Strategy: Regular Full Charge Calibration to Avoid Deep Discharge
It is recommended to perform a slow full charge once a week to help BMS accurately calibrate SOC and prevent battery imbalance. During daily use, discharge not less than 20% to avoid lithium deposition on the negative electrode. When parked for a long time, maintain the battery level at 50% -70% and stay away from high temperature and humid environments.


Reduce fast charging frequency and prioritize using slow charging
Although fast charging is convenient, high current can exacerbate electrolyte aging and thermal stress. It is recommended to use fast charging as an emergency measure and slow charging as much as possible for daily energy replenishment to extend battery life.


Optimize thermal management and BMS algorithm
Adopting a liquid cooling+active heating system to ensure that the battery operates within the optimal temperature range of 0-20 ℃. BMS should have dynamic balancing function, adjust the voltage of each battery cell in real time, and prevent individual battery cells from overloading. Ningde Times Shenxing Battery has been optimized through the synergy of high voltage density and low viscosity electrolyte to enhance low-temperature performance.


Previous: No More Data