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An Ultrafast and Ultra-Low-Temperature Hydrogen Gas-Proton Battery.

Zhengxin ZhuWeiping WangYichen YinYahan MengZaichun LiuTaoli JiangQia PengJifei SunWei Chen
Published in: Journal of the American Chemical Society (2021)
Aqueous proton batteries are regarded as one of the most promising energy technologies for next-generation grid storage due to the distinctive merits of H+ charge carriers with small ionic radius and light weight. Various materials have been explored for aqueous proton batteries; however, their full batteries show undesirable electrochemical performance with limited rate capability and cycling stability. Here we introduce a novel aqueous proton full battery that shows remarkable rate capability, cycling stability, and ultralow temperature performance, which is driven by a hydrogen gas anode and a Prussian blue analogue cathode in a concentrated phosphoric acid electrolyte. Its operation involves hydrogen evolution/oxidation redox reactions on the anode and H+ insertion/extraction reactions on the cathode, in parallel with the ideal transfer of only H+ between these two electrodes. The fabricated aqueous hydrogen gas-proton battery exhibits an unprecedented charge/discharge capability of up to 960 C with a superior power density of 36.5 kW kg-1, along with an ultralong cycle life of over 0.35 million cycles. Furthermore, this hydrogen gas-proton battery is able to work well at an ultralow temperature of -80 °C with 54% of its room-temperature capacity and under -60 °C with a stable cycle life of 1150 cycles. This work provides new opportunities to construct aqueous proton batteries with high performance in extreme conditions for large-scale energy storage.
Keyphrases
  • room temperature
  • ionic liquid
  • solid state
  • electron transfer
  • ion batteries
  • reduced graphene oxide
  • solar cells
  • body mass index
  • carbon dioxide
  • high resolution
  • mass spectrometry
  • quantum dots
  • tandem mass spectrometry