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Keywords = LIB’s protective coatings

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10 pages, 2161 KiB  
Article
TiO2 Coated with Carbon via Chemical Vapor Deposition as Li-Ion Batteries Anode
by Bin Zhu, Wenjun Li, Wu Tang and Hui Tang
Coatings 2024, 14(11), 1473; https://doi.org/10.3390/coatings14111473 - 20 Nov 2024
Cited by 1 | Viewed by 1284
Abstract
With the increasing demand for renewable energy and sustainable technologies, lithium-ion batteries (LIBs) have become crucial energy storage components. Despite the promising properties of the high capacity and stability of TiO2, its large-scale application as an anode for LIBs is hindered [...] Read more.
With the increasing demand for renewable energy and sustainable technologies, lithium-ion batteries (LIBs) have become crucial energy storage components. Despite the promising properties of the high capacity and stability of TiO2, its large-scale application as an anode for LIBs is hindered by challenges like poor conductivity and volumetric changes during cycling. Here, a rutile TiO2 composite material with a thinned carbon coating (TiO2@TC) was synthesized through chemical vapor deposition (CVD) and a subsequent annealing process, which significantly improved the reversibility, cycling stability, and rate performance of the TiO2 anode materials. The thickness of the carbon layer on TiO2 was precisely controlled and thinned from 4.2 nm to 1.9 nm after secondary annealing treatment, leading to a smaller steric hindrance and an improved conductivity while serving as protective coatings by preventing the electrochemical degradation of the TiO2 surface and hindering volumetric changes during cycling. The resulting TiO2@TC with the thin carbon layer demonstrated a high specific capacity of 167 mAh g−1 at 0.5 C in Li-based half cells, which could stably run for 200 cycles with nearly 100% capacity retention. The thin carbon layer also contributes to an improved rate performance of 90 mAh g−1 at even 20 C. This work provides an innovational strategy for improving the conductivity and volumetric changes during the cycling of TiO2 anodes. Full article
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12 pages, 4521 KiB  
Article
Study on the Impact of Air Pressure on the Laser-Induced Breakdown Spectroscopy of Intumescent Fireproof Coatings
by Jun Wang, Honglin Jian, Shouhe Wang, Fengzhen Zhang and Xilin Wang
Appl. Sci. 2024, 14(19), 8765; https://doi.org/10.3390/app14198765 - 28 Sep 2024
Viewed by 1130
Abstract
Intumescent fireproof coatings protect steel structures and cables by forming a thick, fire-resistant layer under high temperatures. These coatings can deteriorate over time, impacting their fire resistance. Current testing methods are largely lab-based, lacking in-service evaluation platforms. Laser-Induced Breakdown Spectroscopy (LIBS) is emerging [...] Read more.
Intumescent fireproof coatings protect steel structures and cables by forming a thick, fire-resistant layer under high temperatures. These coatings can deteriorate over time, impacting their fire resistance. Current testing methods are largely lab-based, lacking in-service evaluation platforms. Laser-Induced Breakdown Spectroscopy (LIBS) is emerging as a promising in situ detection technology but is influenced by low air pressure in high-altitude areas. This study investigates how air pressure affects LIBS signals in intumescent coatings on galvanized steel. Using pressures between 35 and 101 kPa, a linear model was developed to correlate laser pulses to ablation depth for characterizing coating thickness. Results show that spectral intensity decreases with lower air pressure. However, a strong linear relationship persists between laser pulses and ablation depth, with a fitting accuracy above 0.9. The coating thickness is identified by the number of laser pulses required to detect the Zn spectral line from the underlying galvanized steel. As air pressure decreases, the ablation depth increases. The study effectively models and corrects for air pressure effects on LIBS data, enabling its application for field detection of fireproof coatings. This advancement enhances the reliability of LIBS technology in assessing the fire performance of these materials, providing a reference for their in situ evaluation and ensuring better fire safety standards for building steel structures and cables. Full article
(This article belongs to the Special Issue Development and Application of Laser-Induced Breakdown Spectroscopy)
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31 pages, 9263 KiB  
Article
Bubble Wrap-like Carbon-Coated Rattle-Type silica@silicon Nanoparticles as Hybrid Anode Materials for Lithium-Ion Batteries via Surface-Protected Etching
by Angelica Martino, Jiyun Jeon, Hyun-Ho Park, Hochun Lee and Chang-Seop Lee
Batteries 2024, 10(2), 53; https://doi.org/10.3390/batteries10020053 - 1 Feb 2024
Cited by 2 | Viewed by 4236
Abstract
Severe volumetric expansion (~400%) limits practical application of silicon nanoparticles as anode materials for next-generation lithium-ion batteries (LIBs). Here, we describe the fabrication and characterization of a conformal polydopamine carbon shell encapsulating rattle-type silica@silicon nanoparticles (PDA–PEI@PVP–SiO2@Si) with a tunable void structure [...] Read more.
Severe volumetric expansion (~400%) limits practical application of silicon nanoparticles as anode materials for next-generation lithium-ion batteries (LIBs). Here, we describe the fabrication and characterization of a conformal polydopamine carbon shell encapsulating rattle-type silica@silicon nanoparticles (PDA–PEI@PVP–SiO2@Si) with a tunable void structure using a dual template strategy with TEOS and (3-aminopropyl)triethoxysilane (APTES) pretreated with polyvinylpyrrolidone (PVP K30) as SiO2 sacrificial template via a modified Stöber process. Polyethylene imine (PEI) crosslinking facilitated the construction of an interconnected three-dimensional bubble wrap-like carbon matrix structure through hydrothermal treatment, pyrolysis, and subsequent surface-protected etching. The composite anode material delivered satisfactory capacities of 539 mAh g−1 after 100 cycles at 0.1 A g−1, 512.76 mAh g−1 after 200 cycles at 1 A g−1, and 453 mAh g−1 rate performance at 5 A g−1, respectively. The electrochemical performance of PDA–PEI@PVP–SiO2@Si was attributed to the rattle-type structure providing void space for Si volume expansion, PVP K30-pretreated APTES/TEOS SiO2 seeds via catalyst-free, hydrothermal-assisted Stöber protecting Si/C spheres upon etching, carbon coating strategy increasing Si conductivity while stabilizing the solid electrolyte interface (SEI), and PEI carbon crosslinks providing continuous conductive pathways across the electrode structure. The present work describes a promising strategy to synthesize tunable yolk shell C@void@Si composite anode materials for high power/energy-density LIBs applications. Full article
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11 pages, 2401 KiB  
Article
Improved Electrochemical Performance of Li-Rich Cathode Materials via Spinel Li2MoO4 Coating
by Shuhao Zhang, Yun Ye, Zhaoxiong Chen, Qinghao Lai, Tie Liu, Qiang Wang and Shuang Yuan
Materials 2023, 16(16), 5655; https://doi.org/10.3390/ma16165655 - 17 Aug 2023
Cited by 7 | Viewed by 1864
Abstract
Li-rich manganese-based cathode materials (LRMs) are considered one of the most promising cathode materials for the next generation of lithium-ion batteries (LIBs) because of their high energy density. However, there are problems such as a capacity decay, poor rate performance, and continuous voltage [...] Read more.
Li-rich manganese-based cathode materials (LRMs) are considered one of the most promising cathode materials for the next generation of lithium-ion batteries (LIBs) because of their high energy density. However, there are problems such as a capacity decay, poor rate performance, and continuous voltage drop, which seriously limit their large-scale commercial applications. In this work, Li1.2Mn0.54Co0.13Ni0.13O2 coated with Li2MoO4 with a unique spinel structure was prepared with the wet chemistry method and the subsequent calcination process. The Li2MoO4 coating layer with a spinel structure could provide a 3D Li+ transport channel, which is beneficial for improving rate performance, while protecting LRMs from electrolyte corrosion, suppressing interface side reactions, and improving cycling stability. The capacity retention rate of LRMs coated with 3 wt% Li2MoO4 increased from 69.25% to 81.85% after 100 cycles at 1 C, and the voltage attenuation decreased from 7.06 to 4.98 mV per cycle. The lower Rct also exhibited an improved rate performance. The results indicate that the Li2MoO4 coating effectively improves the cyclic stability and electrochemical performance of LRMs. Full article
(This article belongs to the Special Issue Environmentally Friendly Materials)
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21 pages, 3433 KiB  
Article
The Role of Protective Surface Coatings on the Thermal Stability of Delithiated Ni-Rich Layered Oxide Cathode Materials
by Friederike Reissig, Joaquin Ramirez-Rico, Tobias Johannes Placke, Martin Winter, Richard Schmuch and Aurora Gomez-Martin
Batteries 2023, 9(5), 245; https://doi.org/10.3390/batteries9050245 - 25 Apr 2023
Cited by 8 | Viewed by 4284
Abstract
To achieve a broader public acceptance for electric vehicles based on lithium-ion battery (LIB) technology, long driving ranges, low cost, and high safety are needed. A promising pathway to address these key parameters lies in the further improvement of Ni-rich cathode materials for [...] Read more.
To achieve a broader public acceptance for electric vehicles based on lithium-ion battery (LIB) technology, long driving ranges, low cost, and high safety are needed. A promising pathway to address these key parameters lies in the further improvement of Ni-rich cathode materials for LIB cells. Despite the higher achieved capacities and thus energy densities, there are major drawbacks in terms of capacity retention and thermal stability (of the charged cathode) which are crucial for customer acceptance and can be mitigated by protecting cathode particles. We studied the impact of surface modifications on cycle life and thermal stability of LiNi0.90Co0.05Mn0.05O2 layered oxide cathodes with WO3 by a simple sol–gel coating process. Several advanced analytical techniques such as low-energy ion scattering, differential scanning calorimetry, and high-temperature synchrotron X-ray powder diffraction of delithiated cathode materials, as well as charge/discharge cycling give significant insights into the impact of surface coverage of the coatings on mitigating degradation mechanisms. The results show that successful surface modifications of WO3 with a surface coverage of only 20% can prolong the cycle life of an LIB cell and play a crucial role in improving the thermal stability and, hence, the safety of LIBs. Full article
(This article belongs to the Special Issue Li-Ion Battery Materials: Latest Advances and Prospects)
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19 pages, 4489 KiB  
Article
Toward the Improvement of Silicon-Based Composite Electrodes via an In-Situ Si@C-Graphene Composite Synthesis for Li-Ion Battery Applications
by Adrien Mery, Yves Chenavier, Coralie Marcucci, Anass Benayad, John P. Alper, Lionel Dubois, Cédric Haon, Nathalie Herlin Boime, Saïd Sadki and Florence Duclairoir
Materials 2023, 16(6), 2451; https://doi.org/10.3390/ma16062451 - 19 Mar 2023
Cited by 5 | Viewed by 3061
Abstract
Using Si as anode materials for Li-ion batteries remain challenging due to its morphological evolution and SEI modification upon cycling. The present work aims at developing a composite consisting of carbon-coated Si nanoparticles (Si@C NPs) intimately embedded in a three-dimensional (3D) graphene hydrogel [...] Read more.
Using Si as anode materials for Li-ion batteries remain challenging due to its morphological evolution and SEI modification upon cycling. The present work aims at developing a composite consisting of carbon-coated Si nanoparticles (Si@C NPs) intimately embedded in a three-dimensional (3D) graphene hydrogel (GHG) architecture to stabilize Si inside LiB electrodes. Instead of simply mixing both components, the novelty of the synthesis procedure lies in the in situ hydrothermal process, which was shown to successfully yield graphene oxide reduction, 3D graphene assembly production, and homogeneous distribution of Si@C NPs in the GHG matrix. Electrochemical characterizations in half-cells, on electrodes not containing additional conductive additive, revealed the importance of the protective C shell to achieve high specific capacity (up to 2200 mAh.g−1), along with good stability (200 cycles with an average Ceff > 99%). These performances are far superior to that of electrodes made with non-C-coated Si NPs or prepared by mixing both components. These observations highlight the synergetic effects of C shell on Si NPs, and of the single-step in situ preparation that enables the yield of a Si@C-GHG hybrid composite with physicochemical, structural, and morphological properties promoting sample conductivity and Li-ion diffusion pathways. Full article
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19 pages, 16443 KiB  
Article
Al2O3-Coated Si-Alloy Prepared by Atomic Layer Deposition as Anodes for Lithium-Ion Batteries
by Kikang Lee, Sungho Yoon, Sunghoon Hong, Hyunmi Kim, Kyuhwan Oh and Jeongtak Moon
Materials 2022, 15(12), 4189; https://doi.org/10.3390/ma15124189 - 13 Jun 2022
Cited by 13 | Viewed by 3055
Abstract
Silicon-based anodes can increase the energy density of Li-ion batteries (LIBs) owing to their large weights and volumetric capacities. However, repeated charging and discharging can rapidly deteriorate the electrochemical properties because of a large volume change in the electrode. In this study, a [...] Read more.
Silicon-based anodes can increase the energy density of Li-ion batteries (LIBs) owing to their large weights and volumetric capacities. However, repeated charging and discharging can rapidly deteriorate the electrochemical properties because of a large volume change in the electrode. In this study, a commercial Fe-Si powder was coated with Al2O3 layers of different thicknesses via atomic layer deposition (ALD) to prevent the volume expansion of Si and suppress the formation of crack-induced solid electrolyte interfaces. The Al2O3 content was controlled by adjusting the trimethyl aluminum exposure time, and higher Al2O3 contents significantly improved the electrochemical properties. In 300 cycles, the capacity retention rate of a pouch full-cell containing the fabricated anodes increased from 69.8% to 72.3% and 79.1% depending on the Al2O3 content. The powder characterization and coin and pouch cell cycle evaluation results confirmed the formation of an Al2O3 layer on the powder surface. Furthermore, the expansion rate observed during the charging/discharging of the pouch cell indicated that the deposited layer suppressed the powder expansion and improved the cell stability. Thus, the performance of an LIB containing Si-alloy anodes can be improved by coating an ALD-synthesized protective Al2O3 layer. Full article
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51 pages, 12095 KiB  
Review
Remedies to Avoid Failure Mechanisms of Lithium-Metal Anode in Li-Ion Batteries
by Alain Mauger and Christian M. Julien
Inorganics 2022, 10(1), 5; https://doi.org/10.3390/inorganics10010005 - 31 Dec 2021
Cited by 7 | Viewed by 7846
Abstract
Rechargeable lithium-metal batteries (LMBs), which have high power and energy density, are very attractive to solve the intermittence problem of the energy supplied either by wind mills or solar plants or to power electric vehicles. However, two failure modes limit the commercial use [...] Read more.
Rechargeable lithium-metal batteries (LMBs), which have high power and energy density, are very attractive to solve the intermittence problem of the energy supplied either by wind mills or solar plants or to power electric vehicles. However, two failure modes limit the commercial use of LMBs, i.e., dendrite growth at the surface of Li metal and side reactions with the electrolyte. Substantial research is being accomplished to mitigate these drawbacks. This article reviews the different strategies for fabricating safe LMBs, aiming to outperform lithium-ion batteries (LIBs). They include modification of the electrolyte (salt and solvents) to obtain a highly conductive solid–electrolyte interphase (SEI) layer, protection of the Li anode by in situ and ex situ coatings, use of three-dimensional porous skeletons, and anchoring Li on 3D current collectors. Full article
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15 pages, 2982 KiB  
Article
Plasma Enhanced Atomic Layer Deposition of Tantalum (V) Oxide
by Pavel Fedorov, Denis Nazarov, Oleg Medvedev, Yury Koshtyal, Aleksander Rumyantsev, Vladimir Tolmachev, Anatoly Popovich and Maxim Yu Maximov
Coatings 2021, 11(10), 1206; https://doi.org/10.3390/coatings11101206 - 1 Oct 2021
Cited by 3 | Viewed by 4813
Abstract
The tantalum oxide thin films are promising materials for various applications: as coatings in optical devices, as dielectric layers for micro and nanoelectronics, and for thin-films solid-state lithium-ion batteries (SSLIBs). This article is dedicated to the Ta-O thin-film system synthesis by the atomic [...] Read more.
The tantalum oxide thin films are promising materials for various applications: as coatings in optical devices, as dielectric layers for micro and nanoelectronics, and for thin-films solid-state lithium-ion batteries (SSLIBs). This article is dedicated to the Ta-O thin-film system synthesis by the atomic layer deposition (ALD) which allows to deposit high quality films and coatings with excellent uniformity and conformality. Tantalum (V) ethoxide (Ta(OEt)5) and remote oxygen plasma were used as tantalum-containing reagent and oxidizing co-reagent, respectively. The influence of deposition parameters (reactor and evaporator temperature, pulse and purge times) on the growth rate were studied. The thickness of the films were measured by spectroscopic ellipsometry, scanning electron microscopy and X-ray reflectometry. The temperature range of the ALD window was 250–300 °C, the growth per cycle was about 0.05 nm/cycle. Different morphology of films deposited on silicon and stainless steel was found. According to the X-ray diffraction data, the as-prepared films were amorphous. But the heat treatment study shows crystallization at 800 °C with the formation of the polycrystalline Ta2O5 phase with a rhombic structural type (Pmm2). The results of the X-ray reflectometry show the Ta-O films’ density is 7.98 g/cm3, which is close to the density of crystalline Ta2O5 of the rhombic structure (8.18 g/cm3). The obtained thin films have a low roughness and high uniformity. The chemical composition of the surface and bulk of Ta-O coatings was studied by X-ray photoelectron spectroscopy and energy-dispersive X-ray spectroscopy. Surface of the films contain Ta2O5 and some carbon contamination, but the bulk of the films does not contain carbon and any precursor residues. Cyclic voltammetry (CVA) showed that there is no current increase for tantalum (V) oxide in a potential window of 3–4.2 V and has prospects of use as protective coatings for cathode materials of SSLIBs. Full article
(This article belongs to the Special Issue Atomic Layer Deposition: Recent Developments and Future Challenges)
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13 pages, 3300 KiB  
Article
In-Situ Arc Discharge-Derived FeSn2/Onion-Like Carbon Nanocapsules as Improved Stannide-Based Electrocatalytic Anode Materials for Lithium-Ion Batteries
by Dandan Han, Amrita Chatterjee, Long Hin Man and Siu Wing Or
Catalysts 2019, 9(11), 950; https://doi.org/10.3390/catal9110950 - 13 Nov 2019
Cited by 10 | Viewed by 3782
Abstract
Core/shell-structured FeSn2/onion-like carbon (FeSn2/OLC) nanocapsules of confined size range of sub-50 nm are synthesized via an in-situ arc-discharge process, and are evaluated in comparison with FeSn2 nanoparticles as an improved stannide-based electrocatalytic anode material for Li-ion batteries (LIBs). [...] Read more.
Core/shell-structured FeSn2/onion-like carbon (FeSn2/OLC) nanocapsules of confined size range of sub-50 nm are synthesized via an in-situ arc-discharge process, and are evaluated in comparison with FeSn2 nanoparticles as an improved stannide-based electrocatalytic anode material for Li-ion batteries (LIBs). The in-situ arc-discharge process allows a facile one-pot procedure for forming crystalline FeSn2 stannide alloy nanoparticle cores coated by defective OLC thin shells in addition to a confined crystal growth of the FeSn2 nanoparticle cores. The LIB cells assembled using the FeSn2/OLC nanocapsules as the electrocatalytic anodes exhibit superior full specific discharge capacity of 519 mAh·g−1 and specific discharge capacity retention of ~62.1% after 100 charge-discharge cycles at 50 mA·g−1 specific current. The electrochemical stability of FeSn2/OLC nanocapsules is demonstrated from the good cycle stability of the LIBs with a high specific discharge capacity retention of 67.5% on a drastic change in specific current from 4000 to 50 mA·g−1. A formation mechanism is proposed to describe the confined crystal growth of the FeSn2 nanoparticle cores and the formation of the FeSn2/OLC core/shell structure. The observed electrochemical performance enhancement is ascribed to the synergetic effects of the enabling of a reversible lithiation process during charge-discharge of the LIB cells by the FeSn2 nanoparticle cores as well as the protection of the FeSn2 nanoparticle cores from volume change-induced pulverization and solid electrolyte interphase-induced passivation by the OLC shells. Full article
(This article belongs to the Special Issue Metal Nanomaterials for Electrocatalysis)
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