482
Views
6
CrossRef citations to date
0
Altmetric
Research Article

Preparation of Mo-doping LiFePO4/C by carbon reduction method

, &
Pages 419-425 | Received 27 May 2020, Accepted 10 Oct 2020, Published online: 09 Nov 2020
 

ABSTRACT

A Mo-doping LiFe1-xMoxPO4/C cathode material was synthesized via carbothermal reduction route, and the effect of the content of Mo on the structure and electrochemical performance of LiFePO4/C was studied. XRD results revealed doping of Mo did not change the olivine structure of LiFePO4/C, but also formed the Li+ vacancies, which contribute to increase the diffusion rate of Li+. The experimental results further demonstrated that among the Mo-doping samples, the LiFe0.98Mo0.02PO4/C exhibited the best cycle performance and rate performance. After 100 cycles at 0.1 C, its discharge specific capacity reached 143.2 mAh·g−1, which was about 10 mAh·g−1 higher than that of pure phase LiFePO4/C. The capacity retention rate was 98%. When cycling at a rate of up to 5 C, the discharge specific capacity of LiFe0.98Mo0.02PO4/C can still be maintained above 90 mAh·g−1, indicating that Mo doping was an effective method to improve LiFePO4/C electrochemical performance.

Additional information

Funding

This work was supported by the Liaoning Innovation Talents in University (No.LR2017079) and Liaoning Provincial Natural Science Foundation of China (No.2020-BS-154).

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.