21:I[432972,["/_next/static/chunks/bb923814e1f4d2e9.js","/_next/static/chunks/dd3ee9f5b7716ca6.js","/_next/static/chunks/4204a0ae82542ca8.js","/_next/static/chunks/1270dead247da766.js","/_next/static/chunks/6e1aa89a642f40be.js","/_next/static/chunks/2d7aa753e81324a8.js","/_next/static/chunks/8ffd0b71567920d8.js","/_next/static/chunks/67ea6dfd21f16c5f.js","/_next/static/chunks/24eb4379f68013fd.js","/_next/static/chunks/b8cd775ffdf935bd.js","/_next/static/chunks/983103cd9eb7b428.js","/_next/static/chunks/263f2cdcb9aa2341.js","/_next/static/chunks/294b9525248c8e5f.js"],"default"] 22:T566,Abstract Traditional aqueous energy storage devices are difficult to operate at low temperatures owing to the poor ionic conductivity and sluggish interfacial dynamics in frozen electrolytes. Herein, the low‐cost brine refrigerants for food freezing and preservation as electrolytes, and unexpectedly realize high ionic conductivity and stable operation of an aqueous storage device at low temperatures are demonstrated. A CaCl 2 brine refrigerant electrolyte (BRE) with a low freezing point −55 °C and high ionic conductivity (10.1 mS cm −1 at −50 °C) is developed for supercapacitors (SCs), which retains 80% of the room temperature capacity at −50 °C and exhibits ultra‐long cycle life with excellent capacity retention of 92% over 98,500 cycles, outperforming the other SCs which can be operated below −40 °C in literature. Moreover, the SCs with MgCl 2 and NaCl BREs can also be operated successfully with excellent cycle stability and high‐capacity retention at low temperatures of −30 and −20 °C, respectively. Fundamental correlation between various cations and their effect on the freezing point reduction of aqueous electrolytes is revealed via Raman investigation and molecular dynamics simulations. This study provides a rational design strategy for green, inexpensive, and safe low‐temperature aqueous electrolytes for energy storage devices.23:T4de,TiO₂ has drawn increasing research attention as negative electrode material in sodium ion battery because of its natural abundance, low cost, nontoxicity, and facile preparation. Despite tremendous studies carried out, the sodium storage mechanism is still under discussion, and the electronic and local structures of TiO₂ during sodiation/desodiation process are not well understood either. Herein, we reported a mechanism study of graphene-supported oxygen-deficient anatase TiO₂ nanotubes (nanowires) as the negative electrode material for sodium ion batteries. Different from the previous reports, the insertion/extraction of Na⁺ ions leads to almost no changes of titanium valence state but there is a charge redistribution of O 2p orbitals which alters the hybridization between O 2p and Ti 3d states, suggested by the combined electrochemical and X-ray spectroscopic study. Both the electronic and local structures of TiO₂ during the reversible sodiation/desodiation process are revealed from the Ti L-edge and O K-edge spectra. This detailed study would shed light on the material design and structural optimization of TiO₂ as energy storage material in different systems.

#	Concept	H-Index	Publications	Citations
1	Engineering	2	2	61
2	Chemical Engineering	2	2	61
3	Chemistry	2	2	61
4	Materials Science	1	1	45
5	Batteries	1	1	45

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