Affiliation:
1. Department of Applied Chemistry Tokyo University of Science 1‐3 Kagurazaka, Shinjuku‐ku Tokyo 162‐8601 Japan
2. Research Center for Energy and Environmental Materials (GREEN) National Institute for Materials Science (NIMS) 1‐1 Namiki Tsukuba Ibaraki 305‐0044 Japan
Abstract
AbstractHard carbon (HC) is a promising negative‐electrode material for Na‐ion batteries. HC electrochemically stores Na+ ions, resulting in a non‐stoichiometric chemical composition depending on their nanoscale structure, including the carbon framework, and interstitial pores. Therefore, optimizing these structures for Na storage by altering the synthesis conditions can enhance the capacity of Na‐ion batteries. In this study, HCs using MgO, ZnO, and CaCO3 as nanopore templates are systematically investigated, and the ZnO template is found to be particularly effective. By optimizing the concentration of ZnO embedded in the carbon matrix, utilizing a blend of zinc gluconate, and zinc acetate as starting materials, the optimal ZnO‐template HC demonstrates a reversible capacity of 464 mAh g−1 (corresponding to NaC4.8) with high initial coulombic efficiency of 91.7% and low average potential of 0.18 V versus Na+/Na. Thus, a Na‐ion battery full cell consisting of Na5/6Ni1/3Fe1/6Mn1/6Ti1/3O2 and the optimized ZnO‐template HC demonstrates a remarkable energy density of 312 Wh kg−1, comparable to that of a Li‐ion battery with LiFePO4 and graphite. Moreover, the ZnO‐template HC in a K half‐cell also displays a significant capacity of 381 mAh g−1, that is, KC5.8 where the alkali content is higher than stage‐1 graphite intercalation compounds, LiC6 and KC8.
Funder
Japan Society for the Promotion of Science
New Energy and Industrial Technology Development Organization
Japan Science and Technology Agency
Subject
General Materials Science,Renewable Energy, Sustainability and the Environment