posted on 2022-12-19, 19:08authored byYaning Wang, Xiaolin Zhao, Youwei Wang, Wujie Qiu, Erhong Song, Sufan Wang, Jianjun Liu
Even though organic molecules with designed structures
can be assembled
into high-capacity electrode materials, only limited functional groups
such as −CO and −CN– could be
designed as high-voltage cathode materials with enough high capacity.
Here, we propose a common chemical raw material, trinitroaromatic
salt, to have promising potential to develop organic cathode materials
with high discharge voltage and capacity through a strong delocalization
effect between −NO<sub>2</sub> and aromatic ring. Our first-principles
calculations show that electrochemical reactions of trinitroaromatic
potassium salt C<sub>6</sub>H<sub>2</sub>(NO<sub>2</sub>)<sub>3</sub>OK are a 6-electron charge-transfer process, providing a high discharge
capacity of 606 mAh g<sup>–1</sup> and two voltage plateaus
of 2.40 and 1.97 V. Electronic structure analysis indicates that the
discharge process from C<sub>6</sub>H<sub>2</sub>(NO<sub>2</sub>)<sub>3</sub>OK to C<sub>6</sub>H<sub>2</sub>(NO<sub>2</sub>Li<sub>2</sub>)<sub>3</sub>OK stabilizes oxidized [C<sub>6</sub>]<sup><i>n</i>+</sup> to achieve a stable conjugated structure through electron
delocalization from −NO<sub>2</sub> to [C<sub>6</sub>]<sup><i>n</i>+</sup>. The ordered layer structure C<sub>6</sub>H<sub>2</sub>(NO<sub>2</sub>)<sub>3</sub>OK can provide large spatial
pore channels for Li-ion transport, achieving a high ion diffusion
coefficient of 3.41 × 10<sup>–6</sup> cm<sup>2</sup> s<sup>–1</sup>.