| Literature DB >> 34369781 |
Chao Geng1, Tulai Sun2, Zhencui Wang1, Jin-Ming Wu3, Yi-Jie Gu4, Hisayoshi Kobayashi5, Peng Yang1, Jianhang Hai1, Wei Wen1.
Abstract
Hydrogen ion is an attractive charge carrier for energy storage due to its smallest radius. However, hydrogen ions usually exist in the form of hydronium ion (H3O+) because of its high dehydration energy; the choice of electrode materials is thus greatly limited to open frameworks and layered structures with large ionic channels. Here, the desolvation of H3O+ is achieved by using anatase TiO2 as anodes, enabling the H+ intercalation with a strain-free characteristic. Density functional theory calculations show that the desolvation effects are dependent on the facets of anatase TiO2. Anatase TiO2 (001) surface, a highly reactive surface, impels the desolvation of H3O+ into H+. When coupled with a MnO2 cathode, the proton battery delivers a high specific energy of 143.2 Wh/kg at an ultrahigh specific power of 47.9 kW/kg. The modulation of the interactions between ions and electrodes opens new perspectives for battery optimizations.Entities:
Keywords: Crystal plane engineering; Desolvation effect; Energy storage; Hydrogen ion batteries; Titanium dioxide
Year: 2021 PMID: 34369781 DOI: 10.1021/acs.nanolett.1c02421
Source DB: PubMed Journal: Nano Lett ISSN: 1530-6984 Impact factor: 11.189