Abstract Layered oxide cathode with a Li‐O‐vacancy configuration offers high capacity by leveraging additional oxygen redox reactions. However, it faces severe challenges of sluggish kinetics of oxygen redox reactions and lattice oxygen loss, resulting in slow Li+diffusion and rapid electrochemical degradation. Herein, Ti is introduced as electrochemical inactive element into Li‐O‐vacancy configuration to form Mn/vacancy/Ti arrangement within transition metal layers of layered oxide, achieving a marked increase in average output voltage at high current density compared with Ti‐free counterpart. Not only voltage hysteresis between charge and discharge processes can be significantly reduced, but rate capability can be heightened in Li4/7[□1/7Ti1/7Mn5/7]O2by means of retrained over‐potential and improved Li+diffusivity. Furthermore, theoretical calculations suggest that these improvements stem from Ti substitution, which elongates the Li─O bond and lowers the Li+migration energy barrier. Besides, in situ differential electrochemical mass spectrometry and soft X‐ray absorption spectroscopy reveal the modified Li‐O‐vacancy configuration enables reversible anionic and cationic redox behaviors during cycling. These findings provide a promising strategy for tailoring oxygen redox activity and accelerating Li+diffusion kinetics in layered cathode materials with oxygen redox chemistry.
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Structure–Property Relationships in High-Rate Anode Materials Based on Niobium Tungsten Oxide Shear Structures
Nb16W5O55 emerged as a high-rate anode material for Li-ion batteries in 2018 [Griffith et al., Nature2018, 559 (7715), 556−563]. This exciting discovery ignited research in Wadsley−Roth (W−R) compounds, but systematic experimental studies have not focused on how to tune material chemistry and structure to achieve desirable properties for energy storage applications. In this work, we systematically investigate how structure and composition influences capacity, Li-ion diffusivity, charge−discharge profiles, and capacity loss in a series of niobium tungsten oxide W−R compounds: (3 × 4)-Nb12WO33, (4 × 4)-Nb14W3O44, and (4 × 5)-Nb16W5O55. Potentiostatic intermittent titration (PITT) data confirmed that Li-ion diffusivity increases with block size, which can be attributed to an increasing number of tunnels for Li-ion diffusion. The small (3 × 4)-Nb12WO33 block size compound with preferential W ordering on tetrahedral sites exhibits single electron redox and, therefore, the smallest measured capacity despite having the largest theoretical capacity. This observation signals that introducing cation disorder (W occupancy at the octahedral sites in the block center) is a viable strategy to assess multi-electron redox behavior in (3 × 4) Nb12WO33. The asymmetric block size compounds [i.e., (3 × 4) and (4 × 5) blocks] exhibit the greatest capacity loss after the first cycle, possibly due to Li-ion trapping at a unique low energy pocket site along the shear plane. Finally, the slope of the charge−discharge profile increases with increasing block size, likely because the total number of energy-equivalent Li-ion binding sites also increases. This unfavorable characteristic prohibits the large block sizes from delivering constant power at a fixed C-rate more so than the smaller block sizes. Based on these findings, we discuss design principles for Li-ion insertion hosts made from W−R materials.
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- Award ID(s):
- 2046948
- PAR ID:
- 10394421
- Date Published:
- Journal Name:
- ACS Applied Energy Materials
- ISSN:
- 2574-0962
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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null (Ed.)In this investigation, the improved electrochemical behavior in Si-doped Li-rich cathodes is studied with scanning transmission electron microscopy (STEM) and electron energy loss spectroscopy (EELS). Z-contrast images show a layered structure that develops a thin, spinel-like surface layer after the first charge cycle. Si-doping increases discharge capacity by ∼25% and appears to retard the surface phase transformation. Based on electron energy loss spectra, the surface layer in the doped material has an altered oxygen electronic environment, which supports the STEM findings. Furthermore, Si-doping changes the redox behavior during the activation cycle. Density functional theory calculations indicate that Si-doping can increase oxygen vacancy formation, and change the sequence of the redox couples by introducing more oxygen vacancies before or during the typical high voltage activation process. The results of this work indicate that the type of doping employed here is an effective strategy for controlling the complex charge compensation mechanisms in lithium-rich cathodes.more » « less
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In addition, sulfur is a cost effective and environmentally friendly material due to its abundance and low-toxicity. 2 Despite all of these advantages, the practical application of lithium sulfur batteries to date has been hindered by a series of obstacles, including low active material loading, poor cycle life, and sluggish sulfur conversion kinetics. 3 Achieving high mass loading cathode in the traditional 2D planar thick electrode has been challenged. The high distorsion of the traditional planar thick electrodes for ion/electron transfer leads to the limited utilization of active materials and high resistance, which eventually results in restricted energy density and accelerated electrode failure. 4 Furthermore, of the electrolyte to pores in the cathode and utilization ratio of active materials. Catalysts such as MnO 2 and Co dopants were employed to accelerate the sulfur conversion reaction during the charge and discharge process. 5 However, catalysts based on transition metals suffer from poor electronic conductivity. Other catalysts such as transition metal dopants are also limited due to the increased process complexities. . In addition, the severe shuttle effects in Li-S batteries may lead to fast failures of the battery. Constructing a protection layer on the separator for limiting the transmission of soluble polysulfides is considered an effective way to eliminate the shuttle phenomenon. However, the soluble sulfides still can largely dissolve around the cathode side causing the sluggish reaction condition for sulfur conversion. 5 To mitigate the issues above, herein we demonstrate a novel sulfur electrode design strategy enabled by additive manufacturing and oxidative vapor deposition (oCVD). 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Density functional theory calculation reveals the electronic state variance between the structures with and without defects, the structure with defects demonstrates the higher kinetic condition for sulfur conversion. To further identify the favorable reaction dynamic process, the in-situ XRD is used to characterize the transformation between soluble and insoluble polysulfides, which is the main barrier in the charge and discharge process of Li-S batteries. The results show the oCVD coated 3D printed sulfur cathode exhibits a much higher kinetic process for sulfur conversion, which benefits from the highly tailored hierarchal hollow structure and the defects engineering on the cathode. Further, the oCVD coated 3D printed sulfur cathode also demonstrates higher stability during long cycling enabled by the oCVD PEDOT protection layer, which is verified by an absorption energy calculation of polysulfides at PEDOT. Such modeling and analysis help to elucidate the fundamental mechanisms that govern cathode performance and degradation in Li-S batteries. The current study also provides design strategies for the sulfur cathode as well as selection approaches to novel battery systems. References: Bhargav, A., (2020). Lithium-Sulfur Batteries: Attaining the Critical Metrics. Joule 4 , 285-291. Chung, S.-H., (2018). Progress on the Critical Parameters for Lithium–Sulfur Batteries to be Practically Viable. Advanced Functional Materials 28 , 1801188. Peng, H.-J.,(2017). Review on High-Loading and High-Energy Lithium–Sulfur Batteries. Advanced Energy Materials 7 , 1700260. Chu, T., (2021). 3D printing‐enabled advanced electrode architecture design. Carbon Energy 3 , 424-439. Shi, Z., (2021). Defect Engineering for Expediting Li–S Chemistry: Strategies, Mechanisms, and Perspectives. Advanced Energy Materials 11 . Figure 1more » « less
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