Source abstract
Abstract
Theoretically, Cu2O delivers a poor Li storage capacity ∼373.9 mA h g–1 based on a so-called conversion reaction (Cu2O + 2Li → 2Cu + Li2O). Herein, we broke through the bottleneck and acquired an impressive lithium storage capability (1122 mA h g–1) tripled more than the theoretical one by an in situ surface/interface engineering process for the first time. The surface/interface modification enabled us to fabricate ultrasmall nanocrystals of Cu2O with Cu vacancies (VCu) of high concentration, somewhat like monovalent anion doping. Except for the conversion reaction-type capacity, VCu enhancing intercalation pesudocapacitance in Cu2O and its reduction product-Cu also contributed a lot to the Li-storage capability. First-principles calculation substantiated that intercalation energy of Li was severely lowered for both Cu vacancy-rich Cu2O and Cu comparing with their stoichiometric counterparts. Another important factor for the enhancement was the surface/interface organic species themselves which could reversibly store Li by redox reactions. The surface/interface modification for vacancies, vacancy inheritance from metal oxide to single metal, and vacancy-enhancing Li-storage capability in metal oxide and single metal all will inspire us a lot in fabricating new-generation advanced electrodes for rechargeable batteries.
Source: openalex_inverted_index · Quality: baseline
Affiliations
State Key Laboratory of Optoelectronic Materials and Technologies, School of Materials Science and Engineering, Sun Yat-Sen (Zhongshan) University, Guangzhou 510275, People’s Republic of China
Laboratory for Advanced Materials & Electron Microscopy, Beijing National Laboratory for Condensed Matter Physics, Institute of Physics, Chinese Academy of Sciences, Beijing 100190, People’s Republic of China
School of Physics and Electronic Engineering, Jiangsu Normal University, Xuzhou 221116, People’s Republic of China
Funding
National Natural Science Foundation of China