通过 Pd-CN 阴极催化剂的简易石化作用将锂-O2 电池的充电电位降至 3.25 V

Junkai Wang, Daniel Q. Tan, Zhongbo Hu, Xiangfeng Liu
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引用次数: 0

摘要

锂-氧化物电池因其能量密度高而备受关注。然而,高充电电位(∼4.5 V)会导致严重的副反应和安全问题,同时还伴随着往返效率低和循环寿命短的问题。设计催化剂是降低充电电位最常用的策略之一。但降低充电电位的效果非常有限。在此,我们提出了一种独特的 Pd-CN 电化学光化策略,可将锂-氧化物电池的过电位从 4.28 V 显著降至 3.25 V,并揭示了其催化机理。石化作用促进了 CN 中 N 缺陷的形成和锂钯的合金化,从而提高了催化剂的导电性并增加了活性位点的数量。这促进了氧进化反应并降低了过电位。理论计算进一步证明,具有氮空位的电化学调谐 Pd-CN 对锂氧化物的吸附能较弱,从而显著降低了电荷电位。这项研究提出了一种独特而简便的策略来解决锂-氧化物电池中的过电位问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Lowering charge potential of Li-O2 battery to 3.25 V through a facile lithiation of Pd-CN cathode catalyst
Li-O batteries have attracted much attention due to their high energy density. However, the high charging potential (∼4.5 V) causes serious side reactions and safety issues, which are also accompanied by a low round-trip efficiency and poor cycle life. Designing catalysts is one of the most adopted strategies to decrease the charging potential. But the effects of lowering the charging potential are quite limited. Herein, we propose a distinct strategy of electrochemical lithiation of Pd-CN to significantly reduce the overpotential of Li-O batteries from 4.28 V to 3.25 V and reveal the underlying catalysis mechanism. The lithiation promotes the formation of N defects in CN and the alloying of Li-Pd, which improves the conductivity of the catalyst and increases the number of active sites. This promotes the oxygen evolution reaction and decreases the overpotential. Theoretical calculations are further used to prove that the electrochemically tuned Pd-CN with nitrogen vacancies exhibits weak adsorption energy for LiO, enabling a significant reduction in the charge potential. This study proposes a distinct and facile strategy to address the overpotential issue in Li-O batteries.
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