Tuning the Electronic Structure of Niobium Oxyphosphate/Reduced Graphene Oxide Composites by Vanadium-Doping for High-Performance Na+ Storage Application
Zhongteng Chen, Tao Tao, Chenglong Shi, Xiaoyan Shi, Lianyi Shao, Junling Xu, Zhipeng Sun
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引用次数: 0
Abstract
Sodium-ion batteries have become a significant research focus in academia. As a novel sodium anode material, layered NbOPO4, consisting of octahedral NbO6 units sharing oxygen atoms with tetrahedral PO₄ units, exhibits stability due to strong phosphorus-oxygen covalent bonds that prevent oxygen loss from the framework. However, its inherently low electrical conductivity and sluggish charge transfer kinetics limit its electrochemical performance. To address these challenges, we designed and synthesized vanadium-doped niobium oxyphosphate coated with reduced graphene oxide (V-NbOPO4@rGO) via a microwave hydrothermal method followed by calcination. Vanadium doping effectively modulated the electronic structure of NbOPO4 and significantly enhanced its conductivity, as corroborated by density functional theory (DFT) calculations. Consequently, the V0.15-NbOPO4@rGO electrode demonstrated exceptional rate capability, achieving 418 mAh g−1 at a low current density of 0.1 A g−1 and maintaining a reversible capacity exceeding 100 mAh g−1 even at an ultrahigh current density of 50 A g−1. Furthermore, the reversible sodium storage mechanism of V0.15-NbOPO4@rGO was validated through in-situ XRD, TEM, and XPS analyses. This study provides an effective strategy for improving the electrochemical performance of NbOPO4based anodes and deepens understanding of the sodium storage mechanism in V-doped NbOPO4, emphasizing its potential for practical application in sodium-ion batteries.
钠离子电池已成为学术界的一个重要研究热点。作为一种新型的钠阳极材料,层状nbo4由八面体NbO6单元与四面体PO₄单元共享氧原子组成,由于其强大的磷氧共价键可以防止氧从框架中流失,因此具有很强的稳定性。然而,其固有的低电导率和缓慢的电荷转移动力学限制了其电化学性能。为了解决这些挑战,我们设计并合成了钒掺杂的氧化铌包覆还原性氧化石墨烯(V-NbOPO4@rGO),方法是微波水热法,然后煅烧。通过密度泛函理论(DFT)计算证实,钒的掺杂有效地调节了NbOPO4的电子结构,并显著提高了其电导率。因此,V0.15-NbOPO4@rGO电极表现出优异的倍率能力,在0.1 a g−1的低电流密度下达到418 mAh g−1,即使在50 a g−1的超高电流密度下也保持超过100 mAh g−1的可逆容量。此外,通过原位XRD、TEM和XPS分析验证了V0.15-NbOPO4@rGO的可逆储钠机理。本研究为提高NbOPO4基阳极的电化学性能提供了有效的策略,加深了对v掺杂NbOPO4的钠储存机制的理解,强调了其在钠离子电池中的实际应用潜力。