4.7 Article

Tannic Acid as a Small-Molecule Binder for Silicon Anodes

期刊

ACS APPLIED ENERGY MATERIALS
卷 3, 期 7, 页码 6985-6994

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsaem.0c01051

关键词

lithium-ion batteries; silicon anode; tannic acid; hydroxyl groups; small molecule binder; noncovalent interactions

资金

  1. National Science Foundation [1604666, 1604682, CBET-1626418]
  2. National Research Foundation of Korea [NRF-2019R1A2C1004593]
  3. Shared Equipment Authority at Rice University
  4. Directorate For Engineering
  5. Div Of Chem, Bioeng, Env, & Transp Sys [1604666, 1604682] Funding Source: National Science Foundation

向作者/读者索取更多资源

Increasing demand for portable electronic devices, electric vehicles, and grid scale energy storage has spurred interest in developing high-capacity rechargeable lithium-ion batteries (LIBs). Silicon is an abundantly available anode material that has a theoretical gravimetric capacity of 3579 mAh/g and a low operating potential of 0-1 V vs Li/Li+. However, silicon suffers from large volume variation (>300%) during lithiation and delithiation that leads to pulverization, causing delamination from the current collector and battery failure. These issues may be improved by using a binder that hydrogen bonds with the silicon nanoparticle surface. Here, we demonstrate the use of tannic acid, a natural polyphenol, as a binder for silicon anodes in lithium-ion batteries. Whereas the vast majority of silicon anode binders are high molecular weight polymers, tannic acid is explored here as a small molecule binder with abundant hydroxyl (-OH) groups (14.8 mmol of OH/g of tannic acid). This allows for the specific evaluation of hydrogen-bonding interactions toward effective binder performance without the consideration of particle bridging that occurs otherwise with high molecular weight polymers. The resultant silicon electrodes demonstrated a capacity of 850 mAh/g for 200 cycles and a higher capacity when compared to electrodes fabricated by using high molecular weight polymers such as poly(acrylic acid), sodium alginate, and poly(vinylidene fluoride). This work demonstrates that a small molecule with high hydrogen-bonding capability can be used a binder and provides insights into the behavior of small molecule binders for silicon anodes.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

Article Chemistry, Multidisciplinary

Advances in the Chemical Stabilization of MXenes

Swarnima Athavale, Stefano Micci-Barreca, Kailash Arole, Vrushali Kotasthane, Jackson Blivin, Huaixuan Cao, Jodie L. Lutkenhaus, Miladin Radovic, Micah J. Green

Summary: This passage introduces the personal backgrounds and research areas of several graduate students, focusing on the study of MXenes materials.

LANGMUIR (2023)

Article Nanoscience & Nanotechnology

Selective Etching of Ti3AlC2 MAX Phases Using Quaternary Ammonium Fluorides Directly Yields Ti3C2TZ MXene Nanosheets: Implications for Energy Storage

Vrushali Kotasthane, Zeyi Tan, Junyeong Yun, Emily B. Pentzer, Jodie L. Lutkenhaus, Micah J. Green, Miladin Radovic

Summary: MXene synthesis often involves the use of toxic chemicals, limiting its scalability. To overcome this challenge, a safer method is proposed using a mixture of tetramethylammonium fluoride tetrahydrate and hydrochloric acid at room temperature for simultaneous etching and exfoliation. This method results in high MXene yields and MXenes with stable pseudocapacitive behavior and slower degradation rate.

ACS APPLIED NANO MATERIALS (2023)

Article Chemistry, Physical

Molecular mechanisms of pH-tunable stability and surface coverage of polypeptide films

Adam L. Harmat, Maria Morga, Jodie L. Lutkenhaus, Piotr Batys, Maria Sammalkorpi

Summary: Streaming potential and quartz crystal microbalance measurements were used to investigate the pH dependency of the adsorption of poly-L-lysine (PLL) and poly-L-arginine (PARG) on alpha-quartz surface, which was further supported by all-atom molecular dynamics simulations. The adsorption behavior was determined by the change in the number of peptide-surface ion pairs and the repulsive electrostatic interactions between the polypeptides. Low pH favored strong adsorption and stable monolayers, while high pH resulted in weakly bound but denser peptide films with limited stability. Electrostatic interactions, hydrogen bonding, and non-specific interactions played important roles in the adsorption process.

APPLIED SURFACE SCIENCE (2023)

Article Engineering, Environmental

Precise Cation Separations with Composite Cation-Exchange Membranes: Role of Base Layer Properties

Ryan M. DuChanois, Lauren Mazurowski, Hanqing Fan, Rafael Verduzco, Oded Nir, Menachem Elimelech

Summary: The separation of specific ions in water is essential for the recovery and reuse of metals and nutrients, but current membrane technologies lack the required precision selectivity for a circular resource economy. This study investigates whether the cation/cation selectivity of a composite cation-exchange membrane (CEM) is affected by the mass transfer resistance of the underlying CEM. The results show that eliminating resistance from the base layer of the CEM can significantly increase selectivity, highlighting the importance of low-resistance CEMs for precise separations with composite membranes.

ENVIRONMENTAL SCIENCE & TECHNOLOGY (2023)

Article Chemistry, Multidisciplinary

Tailoring the Wettability and Substrate Adherence of Thin Polymer Films with Surface-Segregating Bottlebrush Copolymer Additives

Travis S. S. Laws, Hao Mei, Tanguy Terlier, Rafael Verduzco, Gila E. E. Stein

Summary: Reactive bottlebrush polymers based on S and tBA were developed as additives for PS coatings. The hydrophilicity and substrate adherence of PS films can be controlled by the thermal activation of tBA deprotection. By incorporating a mixture of PtBA and PS side chains into the bottlebrush, the water contact angle decreases and the substrate adherence improves proportionally.

LANGMUIR (2023)

Article Chemistry, Physical

The role of the electrolyte in non-conjugated radical polymers for metal-free aqueous energy storage electrodes

Ting Ma, Cheng-Han Li, Ratul Mitra Thakur, Daniel P. Tabor, Jodie L. Lutkenhaus

Summary: Metal-free aqueous batteries are potential solutions to the shortages of strategic metals and safety issues in lithium-ion batteries. Redox-active non-conjugated radical polymers show promising properties for metal-free aqueous batteries, but their energy storage mechanism in an aqueous environment remains unclear.

NATURE MATERIALS (2023)

Article Polymer Science

Mixed Ionic-Electronic Conduction Increases the Rate Capability of Polynaphthalenediimide for Energy Storage

Yilin Li, Sohee Park, Kasturi Sarang, Hao Mei, Chia-Ping Tseng, Zhiqi Hu, Dongyang Zhu, Xiaoyi Li, Jodie Lutkenhaus, Rafael Verduzco

Summary: Conjugated polymers as battery electrodes have unique and useful properties, and recent research has shown that they can exhibit excellent rate performance due to electron transport. However, increasing the ionic conductivity of conjugated polymer electrodes is currently a challenge. In this study, we investigated a series of conjugated polynapthalene dicarboximide (PNDI) polymers containing oligo(ethylene glycol) (EG) side chains to enhance ion transport. We found that incorporating EG side chains improved both ionic and electronic conductivities, resulting in exceptional rate performance and cycling stability.

ACS POLYMERS AU (2023)

Article Chemistry, Multidisciplinary

Solutions Are the Problem: Ordered Two-Dimensional Covalent Organic Framework Films by Chemical Vapor Deposition

Jeremy P. Daum, Alec Ajnsztajn, Sathvik Ajay Iyengar, Jacob Lowenstein, Soumyabrata Roy, Guan-hui Gao, Esther H. R. Tsai, Pulickel M. Ajayan, Rafael Verduzco

Summary: Covalent organic frameworks (COFs) are a promising class of crystalline polymer networks with high porosity and versatile functionality. A chemical vapor deposition (CVD) approach is developed to produce highly crystalline COF films and coatings in a fast and facile manner. The synthesized COF films are characterized by various techniques and show potential applications in size exclusion membranes, catalytic platforms, and organic transistors.

ACS NANO (2023)

Article Chemistry, Physical

A Synergistic Three-Phase, Triple-Conducting Air Electrode for Reversible Proton-Conducting Solid Oxide Cells

Weilin Zhang, Yucun Zhou, Xueyu Hu, Yong Ding, Jun Gao, Zheyu Luo, Tongtong Li, Nicholas Kane, Xiao-Ying Yu, Tanguy Terlier, Meilin Liu

Summary: Reversible proton-conducting solid oxide cells (R-PSOCs) have the potential to be the most efficient and cost-effective electrochemical device for energy storage and conversion. In this study, researchers developed a class of triple-conducting air electrode materials by doping transition- and rare-earth metal ions into a proton-conducting electrolyte material. These materials showed outstanding activity and durability for R-PSOC applications.

ACS ENERGY LETTERS (2023)

Article Chemistry, Multidisciplinary

Effect of terminal groups on the degradation stability of Ti3C2Tz MXenes

Swarnima Athavale, Stefano A. A. Micci-Barreca, Kailash Arole, Vrushali Kotasthane, Jodie L. L. Lutkenhaus, Miladin Radovic, Micah J. J. Green

Summary: MXenes, as 2D nanomaterials, have attracted significant attention since their discovery in 2011, but their degradation tendency affects their shelf life. While external factors affecting the degradation of MXenes have been extensively studied, the impact of internal factors such as terminal groups remains unclear. In this paper, we compare the degradation stability of MXenes using -Br and -Cl terminations as model terminal groups. Our experiments show that -Br terminated ML-Ti3C2Tz degrades faster than -Cl terminated ML-Ti3C2Tz. We confirm that terminal groups do affect the degradation rate of Ti3C2Tz. The differences in bond dissociation energy of the M-X bond are responsible for the variations in the degradation stability of MXenes. This model study can be generalized to compare the effect of terminal groups on the degradation stability of MXenes.

NANOSCALE (2023)

Article Chemistry, Physical

pH dependence of the assembly mechanism and properties of poly(l-lysine) and poly(l-glutamic acid) complexes

Tuuva Kastinen, Dawid Lupa, Piotr Bonarek, Dmitrii Fedorov, Maria Morga, Markus B. Linder, Jodie L. Lutkenhaus, Piotr Batys, Maria Sammalkorpi

Summary: We demonstrate that pH significantly affects the assembly mechanism and properties of PLL and PGA complexes through a combination of experimental characterization and molecular simulations. Various techniques, including DLS, LDV, ITC, CD, and AUC, are employed to assess the complexation, charge state, thermodynamics, secondary structure, and molecular weights of the peptides. Molecular dynamics simulations provide insights into the binding changes and hydrogen bonding involved in the complex formation. Our findings reveal the pH dependency of PLL/PGA complexation and highlight the potential of pH control in designing peptide materials.

PHYSICAL CHEMISTRY CHEMICAL PHYSICS (2023)

Article Chemistry, Physical

Water-coupled monovalent and divalent ion transport in polyviologen networks

Alexandra D. Easley, Khirabdhi Mohanty, Jodie L. Lutkenhaus

Summary: This study investigates the energy storage mechanism of a cross-linked viologen using electrochemical quartz crystal microbalance with dissipation monitoring (EQCM-D) and compares the effects of NaCl and Na2SO4 electrolytes. The results reveal that electrolyte design and ion valency significantly impact the mass transport properties of polymer-based electrodes. This work provides insights for improving the performance of next-generation polymer batteries through electrolyte selection.

JOURNAL OF MATERIALS CHEMISTRY A (2023)

Article Materials Science, Multidisciplinary

Structural organic battery cathodes comprised of organic redox active polymers, reduced graphene oxide, and aramid nanofibers

Suyash S. Oka, Ratul Mitra Thakur, Alexandra D. Easley, Micah J. Green, Jodie L. Lutkenhaus

Summary: Structural batteries have gained attention due to their multifunctionality and potential for mass and volume savings. This study focuses on using a redox-active polymer as the active material for the cathode, resulting in high rate capabilities and excellent mechanical properties.

MATERIALS ADVANCES (2023)

暂无数据