Bao Zhang , Yi Zhao , Minghuang Li , Qi Wang , Lei Cheng , Lei Ming , Xing Ou , Xiaowei Wang
{"title":"Degradation analysis and doping modification optimization for high-voltage P-type layered cathode in sodium-ion batteries","authors":"Bao Zhang , Yi Zhao , Minghuang Li , Qi Wang , Lei Cheng , Lei Ming , Xing Ou , Xiaowei Wang","doi":"10.1016/j.jechem.2023.10.026","DOIUrl":null,"url":null,"abstract":"<div><p><span><span>Advancing high-voltage stability of layered sodium-ion oxides represents a pivotal avenue for their progress in energy storage applications<span>. Despite this, a comprehensive understanding of the mechanisms underpinning their </span></span>structural deterioration<span> at elevated voltages remains insufficiently explored. In this study, we unveil a layer delamination phenomenon of Na</span></span><sub>0.67</sub>Ni<sub>0.3</sub>Mn<sub>0.7</sub>O<sub>2</sub><span> (NNM) within the 2.0–4.3 V voltage, attributed to considerable volumetric fluctuations along the </span><em>c</em>-axis and lattice oxygen reactions induced by the simultaneous Ni<sup>3+</sup>/Ni<sup>4+</sup> and anion redox reactions. By introducing Mg doping to diminished Ni–O antibonding, the anion oxidation-reduction reactions are effectively mitigated, and the structural integrity of the P2 phase remains firmly intact, safeguarding active sites and precluding the formation of novel interfaces. The Na<sub>0.67</sub>Mg<sub>0.05</sub>Ni<sub>0.25</sub>Mn<sub>0.7</sub>O<sub>2</sub> (NMNM-5) exhibits a specific capacity of 100.7 mA h g<sup>−1</sup><span>, signifying an 83% improvement compared to the NNM material within the voltage of 2.0–4.3 V. This investigation underscores the intricate interplay<span> between high-voltage stability and structural degradation mechanisms in layered sodium-ion oxides.</span></span></p></div>","PeriodicalId":14,"journal":{"name":"ACS Combinatorial Science","volume":null,"pages":null},"PeriodicalIF":3.7840,"publicationDate":"2023-10-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Combinatorial Science","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2095495623005958","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Chemistry","Score":null,"Total":0}
引用次数: 0
Abstract
Advancing high-voltage stability of layered sodium-ion oxides represents a pivotal avenue for their progress in energy storage applications. Despite this, a comprehensive understanding of the mechanisms underpinning their structural deterioration at elevated voltages remains insufficiently explored. In this study, we unveil a layer delamination phenomenon of Na0.67Ni0.3Mn0.7O2 (NNM) within the 2.0–4.3 V voltage, attributed to considerable volumetric fluctuations along the c-axis and lattice oxygen reactions induced by the simultaneous Ni3+/Ni4+ and anion redox reactions. By introducing Mg doping to diminished Ni–O antibonding, the anion oxidation-reduction reactions are effectively mitigated, and the structural integrity of the P2 phase remains firmly intact, safeguarding active sites and precluding the formation of novel interfaces. The Na0.67Mg0.05Ni0.25Mn0.7O2 (NMNM-5) exhibits a specific capacity of 100.7 mA h g−1, signifying an 83% improvement compared to the NNM material within the voltage of 2.0–4.3 V. This investigation underscores the intricate interplay between high-voltage stability and structural degradation mechanisms in layered sodium-ion oxides.
提高层状钠离子氧化物的高压稳定性是其在储能应用中取得进展的关键途径。尽管如此,对其在高电压下结构恶化的机制的全面理解仍然没有得到充分的探索。在这项研究中,我们揭示了Na0.67Ni0.3Mn0.7O2 (NNM)在2.0-4.3 V电压下的层脱层现象,这是由于沿c轴的相当大的体积波动和同时发生的Ni3+/Ni4+和阴离子氧化还原反应引起的晶格氧反应。通过将Mg掺杂到减少的Ni-O反键中,可以有效地减轻阴离子氧化还原反应,并保持P2相的结构完整性,保护活性位点并防止新界面的形成。Na0.67Mg0.05Ni0.25Mn0.7O2 (NMNM-5)的比容量为1007 mA h g−1,在2.0-4.3 V电压范围内,比NNM材料提高了83%。这项研究强调了层状钠离子氧化物中高压稳定性和结构降解机制之间复杂的相互作用。
期刊介绍:
The Journal of Combinatorial Chemistry has been relaunched as ACS Combinatorial Science under the leadership of new Editor-in-Chief M.G. Finn of The Scripps Research Institute. The journal features an expanded scope and will build upon the legacy of the Journal of Combinatorial Chemistry, a highly cited leader in the field.