The thermodynamic origin of hysteresis in insertion batteries.

Lithium batteries are considered the key storage devices for most emerging green technologies such as wind and solar technologies or hybrid and plug-in electric vehicles. Despite the tremendous recent advances in battery research, surprisingly, several fundamental issues of increasing practical importance have not been adequately tackled. One such issue concerns the energy efficiency. Generally, charging of 10(10)-10(17) electrode particles constituting a modern battery electrode proceeds at (much) higher voltages than discharging. Most importantly, the hysteresis between the charge and discharge voltage seems not to disappear as the charging/discharging current vanishes. Herein we present, for the first time, a general explanation of the occurrence of inherent hysteretic behaviour in insertion storage systems containing multiple particles. In a broader sense, the model also predicts the existence of apparent equilibria in battery electrodes, the sequential particle-by-particle charging/discharging mechanism and the disappearance of two-phase behaviour at special experimental conditions.

[1]  Maier,et al.  Simple phenomenological approach to premelting and sublattice melting in Frenkel disordered ionic crystals. , 1995, Physical review. B, Condensed matter.

[2]  P. Bruce,et al.  Rechargeable LI2O2 electrode for lithium batteries. , 2006, Journal of the American Chemical Society.

[3]  Robert Dominko,et al.  Impact of synthesis conditions on the structure and performance of Li2FeSiO4 , 2008 .

[4]  Kristin A. Persson,et al.  First-Principles Investigation of the Li-Fe-F Phase Diagram and Equilibrium and Nonequilibrium Conversion Reactions of Iron Fluorides with Lithium , 2008 .

[5]  Ingo Müller,et al.  Rubber and rubber balloons , 2004 .

[6]  P. Umek,et al.  Tailoring nanostructured TiO2 for high power Li-ion batteries , 2009 .

[7]  Montse Casas-Cabanas,et al.  Room-temperature single-phase Li insertion/extraction in nanoscale Li(x)FePO4. , 2008, Nature materials.

[8]  Palani Balaya,et al.  Anisotropy of Electronic and Ionic Transport in LiFePO4 Single Crystals , 2007 .

[9]  Venkat Srinivasan,et al.  Existence of path-dependence in the LiFePO4 electrode , 2006 .

[10]  C. Delmas,et al.  Lithium deintercalation in LiFePO4 nanoparticles via a domino-cascade model. , 2008, Nature materials.

[11]  Gerbrand Ceder,et al.  Electrochemical modeling of intercalation processes with phase field models , 2004 .

[12]  Byoungwoo Kang,et al.  Battery materials for ultrafast charging and discharging , 2009, Nature.

[13]  Robert Dominko,et al.  Wired Porous Cathode Materials: A Novel Concept for Synthesis of LiFePO4 , 2007 .

[14]  M. Wagemaker,et al.  Large impact of particle size on insertion reactions. A case for anatase Li(x)TiO2. , 2007, Journal of the American Chemical Society.

[15]  S. Boyanov,et al.  P-Redox Mechanism at the Origin of the High Lithium Storage in NiP2-Based Batteries , 2009 .

[16]  Masao Yonemura,et al.  Room-temperature miscibility gap in LixFePO4 , 2006, Nature materials.

[17]  Venkat Srinivasan,et al.  Discharge Model for the Lithium Iron-Phosphate Electrode , 2004 .