Activating and Stabilizing a Reversible four Electron Redox Reaction of I - /I + for Aqueous Zn-Iodine Battery.
Chenggang WangXiaoxing JiJianing LiangShunshun ZhaoXixi ZhangGuangmeng QuWenfeng ShaoChuanlin LiGang ZhaoXijin XuHuiqiao LiPublished in: Angewandte Chemie (International ed. in English) (2024)
Low capacity and poor cycle stability greatly inhibit the development of zinc-iodine batteries. Herein, a high-performance Zn-iodine battery has been reached by designing and optimizing both electrode and electrolyte. The Br - is introduced as the activator to trigger I + , and coupled with I + forming interhalogen to stabilize I + to achieve a four-electron reaction, which greatly promotes the capacity. And the Ni-Fe-I LDH nanoflowers serve as the confinement host to enable the reactions of I - /I + occurring in the layer due to the spacious and stable interlayer spacing of Ni-Fe-I LDH, which effectively suppresses the iodine-species shuttle ensuring high cycling stability. As a result, the electrochemical performance is greatly enhanced, especially in specific capacity (as high as 350 mAh g -1 at 1 A g -1 far higher than two-electron transfer Zn-iodine batteries) and cycling performance (94.6 % capacity retention after 10000 cycles). This strategy provides a new way to realize high capacity and long-term stability of Zn-iodine batteries.
Keyphrases
- electron transfer
- dual energy
- solid state
- heavy metals
- ionic liquid
- signaling pathway
- computed tomography
- metal organic framework
- high intensity
- gold nanoparticles
- magnetic resonance
- immune response
- magnetic resonance imaging
- mass spectrometry
- toll like receptor
- high resolution
- solar cells
- label free
- electron microscopy
- carbon nanotubes
- solid phase extraction