Molecular Engineering towards Safer Lithium-Ion Batteries: A. Highly Stable and Compatible Redox Shuttle for Overcharge.

Similar documents
3,4-Ethylenedioxythiophene (EDOT) and 3,4- Ethylenedioxyselenophene (EDOS): Synthesis and Reactivity of

A dominant homolytic O-Cl bond cleavage with low-spin triplet-state Fe(IV)=O formed is revealed in the mechanism of heme-dependent chlorite dismutase

Supplementary information

Decomposition!of!Malonic!Anhydrides. Charles L. Perrin,* Agnes Flach, and Marlon N. Manalo SUPPORTING INFORMATION

Planar Pentacoordinate Carbon in CAl 5 + : A Global Minimum

SUPPORTING INFORMATION

Aluminum Siting in the ZSM-5 Framework by Combination of

Supporting Information

Supporting Information. for. Silylation of Iron-Bound Carbon Monoxide. Affords a Terminal Fe Carbyne

Supporting Information

Synergistic Effects of Water and SO 2 on Degradation of MIL-125 in the Presence of Acid Gases

Methionine Ligand selectively promotes monofunctional adducts between Trans-EE platinum anticancer drug and Guanine DNA base

Supporting Information

Supporting Information. Copyright Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim, 2008

Electronic Supplementary information

Spin contamination as a major problem in the calculation of spin-spin coupling in triplet biradicals

Phosphine Oxide Jointed Electron Transporters for Reducing Interfacial

Truong Ba Tai, Long Van Duong, Hung Tan Pham, Dang Thi Tuyet Mai and Minh Tho Nguyen*

Supplemental Material

Photoinduced intramolecular charge transfer in trans-2-[4 -(N,Ndimethylamino)styryl]imidazo[4,5-b]pyridine:

Electronic supplementary information (ESI) Infrared spectroscopy of nucleotides in the gas phase 2. The protonated cyclic 3,5 -adenosine monophosphate

Supporting Information. Synthesis, Molecular Structure, and Facile Ring Flipping of a Bicyclo[1.1.0]tetrasilane

Supporting Information. spectroscopy and ab initio calculations of a large. amplitude intramolecular motion

STRUCTURAL DETERMINATION OF A SYNTHETIC POLYMER BY GAUSSIAN COMPUTATIONAL MODELING SOFTWARE

Calculating Accurate Proton Chemical Shifts of Organic Molecules with Density Functional Methods and Modest Basis Sets

Group 13 BN dehydrocoupling reagents, similar to transition metal catalysts but with unique reactivity. Part A: NMR Studies

Supporting Information

Effect of Ionic Size on Solvate Stability of Glyme- Based Solvate Ionic Liquids

Ali Rostami, Alexis Colin, Xiao Yu Li, Michael G. Chudzinski, Alan J. Lough and Mark S. Taylor*

University of Groningen

Electronic Supplementary Information (ESI) for Chem. Commun.

A theoretical study on the thermodynamic parameters for some imidazolium crystals

Electronic Supplementary Information for:

A Redox-Fluorescent Molecular Switch Based on a. Heterobimetallic Ir(III) Complex with a Ferrocenyl. Azaheterocycle as Ancillary Ligand.

Superacid promoted reactions of N-acyliminium salts and evidence for the involvement of superelectrophiles

Metal Enhanced Interactions of Graphene with Monosaccharides. A Manuscript Submitted for publication to. Chemical Physics Letters.

Supporting Information. A rare three-coordinated zinc cluster-organic framework

Supporting Information. O-Acetyl Side-chains in Saccharides: NMR J-Couplings and Statistical Models for Acetate Ester Conformational Analysis

Supporting Information For. metal-free methods for preparation of 2-acylbenzothiazoles and. dialkyl benzothiazole-2-yl phosphonates

Supporting Information For

A Computational Model for the Dimerization of Allene: Supporting Information

Highly sensitive cyanide anion detection with a coumarin-spiropyran conjugate as a fluorescent receptor. Electronic Supplementary Information (ESI )

Supporting Information

China; University of Science and Technology, Nanjing , P R China.

Reversible intercyclobutadiene haptotropism in cyclopentadienylcobalt linear [4]phenylene

Supporting Information. 4-Pyridylnitrene and 2-pyrazinylcarbene

Supporting Information

Supporting Information

Computational Material Science Part II

Supporting Information

Oligo(N-aryl glycines): A New Twist on Structured Peptoids

Scalable synthesis of quaterrylene: solution-phase

Supplementary Material

CICECO, Departamento de Química, Universidade de Aveiro, Aveiro, Portugal

Supporting Information. S1: NMR Spectroscopy and resonance assignments ( 1 H, 13 C)

Supporting information on. Singlet Diradical Character from Experiment

Supporting Information

Concerted halogen and hydrogen bonding in RuI 2 (H 2 dcbpy)(co) 2 ] I 2 (CH 3 OH) I 2 [RuI 2 (H 2 dcbpy)(co) 2 ]

Experimental Evidence for Non-Canonical Thymine Cation Radicals in the Gas Phase

Ferromagnetic Coupling of [Ni(dmit) 2 ] - Anions in. (m-fluoroanilinium)(dicyclohexano[18]crown-6)[ni(dmit) 2 ]

SUPPLEMENTARY INFORMATION

SUPPLEMENTARY INFORMATION

Supporting Information. Detection of Leucine Aminopeptidase Activity in Serum Using. Surface-Enhanced Raman Spectroscopy

Department of Chemistry, School of life Science and Technology, Jinan University, Guangzhou , China b

A phenylbenzoxazole-amide-azacrown linkage as a selective fluorescent receptor for ratiometric sening of Pb(II) in aqueous media

(1) 2. Thermochemical calculations [2,3]

1,5,2,4,6,8-dithiatetrazocine. Synthesis, computation, crystallography and voltammetry of the parent heterocycle. Supplemental Information

Ligand-to-Metal Ratio Controlled Assembly of Nanoporous Metal-Organic Frameworks

Supporting Information

Non-Radiative Decay Paths in Rhodamines: New. Theoretical Insights

Two-Dimensional Carbon Compounds Derived from Graphyne with Chemical Properties Superior to Those of Graphene

Large Hydroazaacene Diimides: Synthesis, Tautomerism, Halochromism, and Redox-switchable NIR Optics

Electrophilicity and Nucleophilicity of Commonly Used. Aldehydes

Supporting Information

Gold Catalyzed Reduction of a Hexavalent Aromatic Sulfonyl Phthalimide to Sulfur

Supporting Information. Copyright Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim, 2006

Supporting information

SUPPORTING INFORMATION. Ammonia-Borane Dehydrogenation Promoted by a Pincer-Square- Planar Rhodium(I)-Monohydride: A Stepwise Hydrogen Transfer

Molecular Modeling of Photoluminescent Copper(I) Cyanide Materials. Jasprina L Ming Advisor: Craig A Bayse

Ionic liquid electrolytes for reversible magnesium electrochemistry

Supporting Information

Reaction of N-(4-methyl-6-oxo-1,6-dihydropyrimidin-2-yl)guanidine with benzaldehyde: experimental and theoretical investigation of the product

Concerted Attack of Frustrated Lewis Acid Base Pairs on Olefinic Double Bonds: A Theoretical Study

Supporting Information. Fluorescent Coronene Monoimide Gels via H-bonding Induced Frustrated Dipolar Assembly

Tuning the electron transport band gap of bovine serum. albumin by doping with Vb12

Supporting Information

Supporting Information

1,4-Benzene-Bridged Covalent Hybrid of Triarylamine and Cyclometalated Ruthenium: A New Type of Organic-Inorganic Mixed-Valent System

Supporting Information. {RuNO} 6 vs. Co-Ligand Oxidation: Two Non-Innocent Groups in One Ruthenium Nitrosyl Complex

Supporting information

Supporting Information

» ß π«õß 1 H-NMR 13 C-NMR ª ªï Õß

Supporting Information. for. Angew. Chem. Int. Ed. Z Wiley-VCH 2003

Supporting Information

Which NICS Aromaticity Index for Planar π Rings is Best?

Motooka, Nishi, Fukuoka , Japan.

Electronic Supplementary Information. Electron Mobility for All-Polymer Solar Cells

The Activation of Carboxylic Acids via Self Assembly Asymmetric Organocatalysis: A Combined Experimental and Computational Investigation

The Chemist Journal of the American Institute of Chemists

Supporting Information

Transcription:

Supporting Information Molecular Engineering towards Safer Lithium-Ion Batteries: A Highly Stable and Compatible Redox Shuttle for vercharge Protection Lu Zhang, Zhengcheng Zhang,*, Paul C. Redfern, Larry A. Curtiss, and Khalil Amine*,1 Chemical Sciences and Engineering Division, Material Sciences Division, Argonne National Laboratory 9700 South Cass Avenue, Argonne, IL 60439, USA E-mail: zzhang@anl.gov; amine@anl.gov Experiments: 1. Synthesis 1,4-di-tert-butyl-2,5-bis(2-methoxyethoxy)methoxybenzene (DBMEB) and 1,4-bis(2- methoxyethoxy)-2,5-di-tert-butylbenzene (DBBB) are not commercially available and were synthesized in our lab according to the following procedure (Figure S1). 2,5-di-tertbutylhydroquinone (9 mmol) was dissolved in anhydrous THF (20 ml). Sodium hydride (27 mmol) and 2-methoxyethoxymethyl chloride or 2-chloroethyl methyl ether (18 mmol) was added to the solution. The reaction was stirred at room temperature for overnight.

After removal of the solvent, the residue was partitioned between dichloromethane (DCM) and NaHC 3 (0.1 M). The organic portion was separated and dried over Na 2 S 4 before solvent was removed under vacuum. The crude product was chromatographed (silica, hexanes/dcm from 5:1 to 1:1) to afford oligo(ethylene glycol) functionalized compounds, which were further purified by crystallization from saturated dichloromethane solution under low temperature. For DBMEB, the yield was 65% and it has been fully characterized by the following methods: 1 H NMR (300 MHz, CDCl 3 ): /ppm 7.14 (s, 2H), 5.25 (s, 4H), 3.86 (t, J = 4.5 Hz, 4H), 3.60 (t, J = 4.5 Hz, 4H), 3.40 (s, 6H), 1.36 (s, 18 H); 13 C NMR (125 MHz, CDCl 3 ): /ppm 151.01, 137.00, 114.53, 94.37, 71.93, 67.53, 59.26, 34.80; Mass spectroscopy (EI + ): calcd. (M+Na) + 421.2561, found (M+Na) + 421.2562. H H + 2 Cl NaH THF H H + 2 Cl NaH THF Figure S1. Synthesis routes of 1,4-di-tert-butyl-2,5-bis(2- methoxyethoxy)methoxybenzene (DBMEB) and 1,4-bis(2-methoxyethoxy)-2,5-di-tertbutylbenzene (DBBB).

Figure S2. 1 H-NMR spectrum of the DBMEB. Figure S3. 13 C-NMR spectrum of the DBMEB.

Figure S4. Mass spectrum of the DBMEB. For DBBB, the yield was 70% and it has been fully characterized by the following methods: 1 H NMR (300 MHz, CDCl 3 ): /ppm 6.86 (s, 2H), 4.14 (t, J = 1.5 Hz, 4H), 3.79 (t, J = 1.5 Hz, 4H), 3.47 (s, 6H), 1.39 (s, 18 H); 13 C NMR (125 MHz, CDCl 3 ): /ppm 151.53, 136.76, 112.82, 71.89, 68.28, 59.41, 34.95; Melting point: 69.3-70.1 o C; Mass spectroscopy (EI + ): calcd. (M+Na) + 361.2364, found (M+Na) + 361.2365.

Figure S5. 1 H-NMR spectrum of the DBBB. Figure S6. 13 C-NMR spectrum of the DBBB.

Figure S7. Mass spectrum of the DBBB. 2. Electrochemical measurements Cyclic voltammetry (CV) experiments were performed in custom-made three electrode cells with 1 mm diameter Pt working electrode, a Li metal reference electrode, and a Li counter electrode using Solartron Analytical 1470E system. The overcharge test was conducted by assembling LiFeP 4 /graphite 2032 coin cells. Graphite electrode used is mesocarbon microbeads (MCMB). The lamination of LiFeP 4 electrode is composed of 80% LiFeP 4 active material, 12% acetylene carbon black and 8% PVDF as binder. The electrolyte used was 1.2 M LiPF 6 in EC/EMC in a weight ratio of 3:7 (Gen 2 electrolyte). The concentrations of the shuttle molecule varied from 0.1 M to 0.4 M. The cells were charged using a constant current to 200% capacity (100% overcharge ratio) or until a specific upper cutoff voltage was reached (normally 4.95V vs Li/Li + ), whichever occurred first. After the charging process, the cells were discharged to a normal cutoff voltage using the same constant current.

3. Computational Methods B3LYP calculations were performed with Gaussian 03 1. Free energies were calculated as follows. B3LYP/6-31G* optimization and frequency calculations were performed followed by PCM SCRF calculations at the B3LYP/6-31+G* level with modified water solvent. A dielectric constant of 55.725 was used to represent a typical 25% EC/25% ethyl methyl carbonate/50% PC electrolyte. B3LYP/6-311+g(3df,2p) energies were then calculated to account for the effects of a larger basis set. 4. Diffusion coefficient Diffusion coefficient is an important parameter to evaluate the efficiency of the charge shunting process of redox shuttles. Figure S9 plots the anodic peak current (I p ) versus the square root of the sweep rates (ν 1/2 ). The resulting slope was then substituted into the Randles-Sevcik 2 equation (1) to calculate the diffusion coefficient, where I p is the anodic peak current, n is the number of electrons involved in the redox process, C is the concentration of redox shuttle and D is the diffusion coefficient. The linear slope derived from Figure S9 suggests diffusion-controlled redox chemistry. The calculated diffusion coefficient for DBBB is 9.26 10-7 cm/s. i p = (269,000)n 3/2 AD 1/2 Cν 1/2 (1)

I AP (A 1e-5 ) Electronic Supplementary Material (ESI) for Energy & Environmental Science 12 data ponits Linear Fit 8 4 y = a + b*x Equation No Weighting Weight 2.80096E-11 Residual Sum of Squares Pearson's r 0.99731 Adj. R-Square 0.99284 Value Standard Error B Intercept 1.42047E-5 2.87803E-6 B Slope 1.62663E-4 6.89963E-6 0 0.0 0.2 0.4 0.6 0.8 (dv/dt) 1/2 (V/sec) 1/2 Figure S9. Plot of I p vs. ν 1/2 used for determination of diffusion constant. Figure S10. Voltage profiles of overcharge abuse tests using Li/LiFeP 4 coin cells containing 0.1 M DBBB in Gen 2 electrolyte during the course of 0-3000 h. Charging rate is C/10 and overcharge ratio is 100%.

Discharge capacity (mah) Capacity (mah) Capacity (mah) Electronic Supplementary Material (ESI) for Energy & Environmental Science 4 4 3 3 2 a 2 b 1 Charge capacity Discharge capacity 0 0 20 40 60 80 100 Cycle number 1 Charge capacity Discharge capacity 0 0 20 40 60 80 100 Cycle number Figure S11. Capacity profiles of overcharge abuse tests using MCMB/ LiFeP 4 (a) and Li/LiFeP 4 (b) coin cells containing 0.1 M DBBB in Gen 2 electrolyte. Charging rate is C/10 and overcharge ratio is 100%. The difference of charge and discharge capacity comes from the electricity shunted by redox shuttle additive during overcharge. 2.0 1.5 1.0 Gen 2 electrolyte 0.35 M ANL-2 in Gen 2 electrolyte 0.5 0.0 0 50 100 150 200 Cycle number Figure S12. Capacity retention profiles of normal cycle tests using MCMB/LiFeP 4 coin cells containing none or 0.35 M DBBB in Gen 2 electrolyte. Charging rate is C/3 and cut off voltage is 2.3 ~3.6 V.

Reference: (1) M. J. Frisch, G. W. T., H. B. Schlegel, G. E. Scuseria, M. A. Robb, J. R. Cheeseman, J. A. Montgomery, Jr., T. Vreven, K. N. Kudin, J. C. Burant, J. M. Millam, S. S. Iyengar, J. Tomasi, V. Barone, B. Mennucci, M. Cossi, G. Scalmani, N. Rega, G. A. Petersson, H. Nakatsuji, M. Hada, M. Ehara, K. Toyota, R. Fukuda, J. Hasegawa, M. Ishida, T. Nakajima, Y. Honda,. Kitao, H. Nakai, M. Klene, X. Li, J. E. Knox, H. P. Hratchian, J. B. Cross, V. Bakken, C. Adamo, J. Jaramillo, R. Gomperts, R. E. Stratmann,. Yazyev, A. J. Austin, R. Cammi, C. Pomelli, J. W. chterski, P. Y. Ayala, K. Morokuma, G. A. Voth, P. Salvador, J. J. Dannenberg, V. G. Zakrzewski, S. Dapprich, A. D. Daniels, M. C. Strain,. Farkas, D. K. Malick, A. D. Rabuck, K. Raghavachari, J. B. Foresman, J. V. rtiz, Q. Cui, A. G. Baboul, S. Clifford, J. Cioslowski, B. B. Stefanov, G. Liu, A. Liashenko, P. Piskorz, I. Komaromi, R. L. Martin, D. J. Fox, T. Keith, M. A. Al-Laham, C. Y. Peng, A. Nanayakkara, M. Challacombe, P. M. W. Gill, B. Johnson, W. Chen, M. W. Wong, C. Gonzalez, and J. A. Pople, Gaussian, Inc., Wallingford CT, 2004. 2003. (2) Feng, J. K.; Ai, X. P.; Cao, Y. L.; Yang, H. X. Electrochemistry Communications 2007, 9, 25.