Nanoarchitectonics of the cathode to improve the reversibility of Li–O₂ batteries

• Hien Thi Thu Pham,
• Jonghyeok Yun,
• So Yeun Kim,
• Sang A Han,
• Jung Ho Kim,
• Jong-Won Lee and
• Min-Sik Park

Beilstein J. Nanotechnol. 2022, 13, 689–698, doi:10.3762/bjnano.13.61

• -trip efficiency and cycling performance of nonaqueous lithium–oxygen batteries are governed by minimizing the discharge products, such as Li2O and Li2O2. Recently, a metal–organic framework has been directly pyrolyzed into a carbon frame with controllable pore volume and size. Furthermore, selective

• for lowering the overpotential of the cathode during cycling, even at the high current density of 2,000 mA·g−1. Keywords: cathode composition; electrochemistry; Li–O2 battery; metal–organic framework; nanoarchitectonics; zeolitic imidazolate framework; Introduction Recently, lithium–oxygen batteries

Self-standing heterostructured NiC_x-NiFe-NC/biochar as a highly efficient cathode for lithium–oxygen batteries

• Shengyu Jing,
• Xu Gong,
• Shan Ji,
• Linhui Jia,
• Bruno G. Pollet,
• Sheng Yan and
• Huagen Liang

Beilstein J. Nanotechnol. 2020, 11, 1809–1821, doi:10.3762/bjnano.11.163

• , Norway Shanghai Time Shipping CO., LTD, Shanghai, 200126, China 10.3762/bjnano.11.163 Abstract Lithium–oxygen batteries have attracted research attention due to their low cost and high theoretical capacity. Developing inexpensive and highly efficient cathode materials without using noble metal-based

• catalysts is highly desirable for practical applications in lithium–oxygen batteries. Herein, a heterostructure of NiFe and NiCx inside of N-doped carbon (NiCx-NiFe-NC) derived from bimetallic Prussian blue supported on biochar was developed as a novel self-standing cathode for lithium–oxygen batteries. The

• . The structure of NiCx-NiFe-NC efficiently improved the electron and ion transfer between the cathode and the electrolyte during the electrochemical processes, resulting in superior electrocatalytic properties in lithium–oxygen batteries. This study indicates that nickel carbide supported on N-doped

From lithium to sodium: cell chemistry of room temperature sodium–air and sodium–sulfur batteries

• Philipp Adelhelm,
• Pascal Hartmann,
• Conrad L. Bender,
• Martin Busche,
• Christine Eufinger and
• Juergen Janek

Beilstein J. Nanotechnol. 2015, 6, 1016–1055, doi:10.3762/bjnano.6.105

• . This review provides a summary of the state-of-the-art knowledge on lithium–sulfur and lithium–oxygen batteries and a direct comparison with the analogous sodium systems. The general properties, major benefits and challenges, recent strategies for performance improvements and general guidelines for

• concerned with lithium–oxygen batteries. The cell concepts are entirely different from conventional Li-ion technology, as depicted in Figure 2. Here, elemental sulfur and atmospheric oxygen are reduced at the positive electrode to form Li2S and Li2O2 during discharge, which is expressed by: Moreover, the

• limit is reached. The need to protect the lithium anode from direct contact with water is experimentally challenging, so most research has been devoted to lithium–oxygen batteries with an aprotic electrolyte. Some possible discharge products can be directly predicted from the Li–O phase diagram shown in