通过高频 Na+ 激活稳定的多电子转移跳跃到一个 Sc-doped Na3.97VMn0.97Sc0.03(PO4) 3
Hui Gao1,2, Cheng Peng2, Rui Xu2
1School of Materials Science and Engineering, Dalian Jiaotong University, Dalian, 116028, China.
Small (Weinheim an der Bergstrasse, Germany)
|August 14, 2025
概括
兴奋剂通过激活多电子转移和改善动力学来提高离子电池阴极容量. 这种修改提高了下一代储能系统的性能和稳定性.
科学领域:
- 材料科学 材料科学 材料科学
- 电化学 电化学 电化学
- 储能 储能 储能 储能 储能 储能
背景情况:
- 离子电池 (SIB) 对储能充满希望,但正极容量限制阻碍了它们的广泛采用.
- Na4VMn(PO4) 3 (NVMP) 阴极显示出潜力,但在其原生V3+/V4+和Mn2+/Mn3+氧化还原对中遭受缓慢动力学的影响.
- 激活像V4+/V5+这样的更高价值状态可以增加容量,但通常需要高潜力 (>4.0 V vs Na+/Na),并导致结构不稳定.
研究的目的:
- 设计一个修改后的NVMP阴极,激活多电子转移以获得更高的容量.
- 为了增强电化学动力学和改善在稳定的电压范围内的氧化还原反应的可逆性.
- 调查兴奋剂在改善Na+扩散和循环稳定性方面的作用.
主要方法:
- 合成与 (Sc) 合的Na3.97VMn0.97Sc0.03(PO4) 3材料.
- 电化学表征包括循环电压测量和静电循环来评估容量和动力学.
- 在循环过程中分析Na+扩散机制和结构稳定性.
主要成果:
- 通过启用2.05电子传输,sc-doped NVMP实现了16.7%的容量增加,达到113.8 mAh g-1.
- V3+/V4+和Mn2+/Mn3+的氧化还原反应在2.0-3.8V范围内加速,改善了动力学.
- 由于Sc诱导的VNa'空缺,增强的Na+扩散动力学导致了优异的容量保留 (80.2%在5C下1400个循环后).
结论:
- 兴奋剂有效地激活了NVMP阴极中的多电子转移,同时保持了结构完整性.
- 该策略提供了合理的电压窗口,减轻了与高潜力氧化还原对相关的可逆性问题.
- 这项工作为SIBs开发高性能,稳定的多电子转移阴极提供了一种可行的方法.
更多相关视频
08:30Monovalent Cation Doping of CH3NH3PbI3 for Efficient Perovskite Solar Cells
Published on: March 19, 2017
16.8K
06:49Radio Frequency Magnetron Sputtering of GdBa2Cu3O7âˆ'ÃŽ ´/ La0.67Sr0.33MnO3 Quasi-bilayer Films on SrTiO3 STO Single-crystal Substrates
Published on: April 12, 2019
7.7K
相关概念视频
Electron Configuration of Multielectron Atoms
54.3K
The alkali metal sodium (atomic number 11) has one more electron than the neon atom. This electron must go into the lowest-energy subshell available, the 3s orbital, giving a 1s22s22p63s1 configuration. The electrons occupying the outermost shell orbital(s) (highest value of n) are called valence electrons, and those occupying the inner shell orbitals are called core electrons. Since the core electron shells correspond to noble gas electron configurations, we can abbreviate electron...
54.3K
Colors and Magnetism
12.3K
Color in Coordination Complexes
When atoms or molecules absorb light at the proper frequency, their electrons are excited to higher-energy orbitals. For many main group atoms and molecules, the absorbed photons are in the ultraviolet range of the electromagnetic spectrum, which cannot be detected by the human eye. For coordination compounds, the energy difference between the d orbitals often allows photons in the visible range to be absorbed and emitted, which is seen as colors by the human...
When atoms or molecules absorb light at the proper frequency, their electrons are excited to higher-energy orbitals. For many main group atoms and molecules, the absorbed photons are in the ultraviolet range of the electromagnetic spectrum, which cannot be detected by the human eye. For coordination compounds, the energy difference between the d orbitals often allows photons in the visible range to be absorbed and emitted, which is seen as colors by the human...
12.3K
Atomic Nuclei: Nuclear Relaxation Processes
723
In the absence of an external magnetic field, nuclear spin states are degenerate and randomly oriented. When a magnetic field is applied, the spins begin to precess and orient themselves along (lower energy) or against (higher energy) the direction of the field. At equilibrium, a slight excess population of spins exists in the lower energy state. Because the direction of the magnetic field is fixed as the z-axis, the precessing magnetic moments are randomly oriented around the z-axis.
723
Valence Bond Theory
9.7K
Coordination compounds and complexes exhibit different colors, geometries, and magnetic behavior, depending on the metal atom/ion and ligands from which they are composed. In an attempt to explain the bonding and structure of coordination complexes, Linus Pauling proposed the valence bond theory, or VBT, using the concepts of hybridization and the overlapping of the atomic orbitals. According to VBT, the central metal atom or ion (Lewis acid) hybridizes to provide empty orbitals of suitable...
9.7K
SN2 Reaction: Transition State
10.2K
An SN2 reaction of an alkyl halide is a single-step process in which bond formation between the nucleophile and the substrate and bond breaking between the substrate and the halide occurs simultaneously through a transition state without forming an intermediate.
When the nucleophile approaches the electrophilic carbon with its lone pairs, the halide acts as a leaving group and moves away with the electron-pair bonded to the carbon. Dotted partial bonds represent the bonds being formed or broken...
When the nucleophile approaches the electrophilic carbon with its lone pairs, the halide acts as a leaving group and moves away with the electron-pair bonded to the carbon. Dotted partial bonds represent the bonds being formed or broken...
10.2K
Nuclear Transmutation
18.0K
Nuclear transmutation is the conversion of one nuclide into another. It can occur by the radioactive decay of a nucleus, or the reaction of a nucleus with another particle. The first manmade nucleus was produced in Ernest Rutherford’s laboratory in 1919 by a transmutation reaction, the bombardment of one type of nuclei with other nuclei or with neutrons. Rutherford bombarded nitrogen-14 atoms with high-speed α particles from a natural radioactive isotope of radium and observed...
18.0K
