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Low temperature rechargeable batteries are important to life in cold climates, polar/deep-sea expeditions and space explorations. Here, we report ~ 3.5 - 4 V rechargeable lithium/chlorine (Li/Cl2) batteries operating down to -80 {\deg}C, employing Li metal negative electrode, a novel CO2 activated porous carbon (KJCO2) as the positive electrode, and a high ionic conductivity (~ 5 to 20 mS cm-1 from -80 {\deg}C to 25 {\deg}C) electrolyte comprised of 1 M aluminum chloride (AlCl3), 0.95 M lithium chloride (LiCl), and 0.05 M lithium bis(fluorosulfonyl)imide (LiFSI) in low melting point (-104.5 {\deg}C) thionyl chloride (SOCl2). Between room-temperature and -80 {\deg}C, the Li/Cl2 battery delivered up to ~ 30,000 - 4,500 mAh g-1 first discharge capacity and a 1,200 - 5,000 mAh g-1 reversible capacity (discharge voltages in ~ 3.5 to 3.1 V) over up to 130 charge-discharge cycles. Mass spectrometry and X-ray photoelectron spectroscopy (XPS) probed Cl2 trapped in the porous carbon upon LiCl electro-oxidation during charging. At lower temperature down to -80 {\deg}C, SCl2/S2Cl2 and Cl2 generated by electro-oxidation in the charging step were trapped in porous KJCO2 carbon, allowing for reversible reduction to afford a high discharge voltage plateau near ~ 4 V with up to ~ 1000 mAh g-1 capacity for SCl2/S2Cl2 reduction and up to ~ 4000 mAh g-1 capacity at ~ 3.1 V plateau for Cl2 reduction. Towards practical use, we made CR2032 Li/Cl2 battery cells to drive digital watches at -40 {\deg}C and light emitting diode at -80 {\deg}C, opening Li/Cl2 secondary batteries for ultra-cold conditions.

Advancing new ideas of rechargeable batteries represents an important path to meeting the ever increasing energy storage needs. Recently we showed rechargeable sodium/chlorine (Na/Cl$_2$) (or lithium/chlorine Li/Cl$_2$) batteries that used a Na (or Li) metal negative electrode, a microporous amorphous carbon nanosphere (aCNS) positive electrode and an electrolyte containing dissolved AlCl$_3$ and fluoride additives in thionyl chloride (SOCl$_2$). The main battery redox reaction involved conversion between NaCl and Cl$_2$ trapped in the carbon positive electrode, delivering a cyclable capacity of up to 1200 mAh g$^{-1}$ (based on positive electrode mass) at a ~ 3.5 V discharge voltage. Here, we discovered by X-ray photoelectron spectroscopy (XPS) that upon charging a Na/Cl$_2$ battery, chlorination of carbon in the positive electrode occurred to form C-Cl accompanied by molecular Cl$_2$ infiltrating the porous aCNS, consistent with Cl$_2$ probed by mass spectrometry. Synchrotron X-ray diffraction observed the development of graphitic ordering in the initially amorphous aCNS under battery charging when the carbon matrix was oxidized/chlorinated and infiltrated with Cl$_2$. The C-Cl, Cl$_2$ species and graphitic ordering were reversible upon discharge, accompanied by NaCl formation. The results revealed redox conversion between NaCl and Cl$_2$, reversible graphitic ordering/amorphourization of carbon through battery charge/discharge, and for the first time probed trapped Cl$_2$ in porous carbon by XPS., Comment: 30 pages, 9 figures

Developing new types of high-capacity and high-energy density rechargeable battery is important to future generations of consumer electronics, electric vehicles, and mass energy storage applications. Recently we reported ~ 3.5 V sodium/chlorine $(Na/Cl_2)$ and lithium/chlorine $(Li/Cl_2)$ batteries with up to 1200 mAh $g^{-1}$ reversible capacity, using either a Na or Li metal as the negative electrode, an amorphous carbon nanosphere (aCNS) as the positive electrode, and aluminum chloride $(AlCl_3)$ dissolved in thionyl chloride $(SOCl_2)$ with fluoride-based additives as the electrolyte. The high surface area and large pore volume of aCNS in the positive electrode facilitated NaCl or LiCl deposition and trapping of $Cl_2$ for reversible $NaCl/Cl_2$ or $LiCl/Cl_2$ redox reactions and battery discharge/charge cycling. Here we report an initially low surface area/porosity graphite (DGr) material as the positive electrode in a $Li/Cl_2$ battery, attaining high battery performance after activation in carbon dioxide $(CO_2)$ at 1000 {\deg}C (DGr_ac) with the first discharge capacity ~ 1910 mAh $g^{-1}$ and a cycling capacity up to 1200 mAh $g^{-1}$. Ex situ Raman spectroscopy and X-ray diffraction (XRD) revealed the evolution of graphite over battery cycling, including intercalation/de-intercalation and exfoliation that generated sufficient pores for hosting $LiCl/Cl_2$ redox. This work opens up widely available, low-cost graphitic materials for high-capacity alkali metal/$Cl_2$ batteries. Lastly, we employed mass spectrometry to probe the $Cl_2$ trapped in the graphitic positive electrode, shedding light into the $Li/Cl_2$ battery operation., Comment: 37 pages, 16 figures, 1 table