Graphene Oxide: Stable Carbon Framework for Functionalization Siegfried Eigler,* a Stefan Grimm, a Ferdinand Hof, a Andreas Hirsch a

Similar documents
Supporting Information. Controlled Functionalization of Graphene Oxide with Sodium Azide

Investigation of the Thermal Stability of the Carbon Framework of Graphene Oxide

Skalierbare Oxo-Funktionalisierung von sp 2 -hybridisierten Kohlenstoffallotropen

SUPPLEMENTARY INFORMATION

Photocatalytic degradation of dyes over graphene-gold nanocomposites under visible light irradiation

Iodide-mediated room temperature reduction of graphene oxide: a rapid chemical route for the synthesis of a bifunctional electrocatalyst

Solution-processable graphene nanomeshes with controlled

Surfactant-free exfoliation of graphite in aqueous solutions

Graphene Oxide / Polyaniline Nanostructures: Transformation of 2D sheet to 1D Nanotube and in-situ Reduction

Supporting Information

Supporting Information

The GO was synthesized by oxidation of purified natural small graphite and graphite

SUPPORTING INFORMATION

The photoluminescent graphene oxide serves as an acceptor rather. than a donor in the fluorescence resonance energy transfer pair of

Supporting Information

Synthesis of a highly conductive and large surface area graphene oxide hydrogel and its use in a supercapacitor

Supporting Information

Growth of 2D sheets of a MOF on graphene surfaces to yield composites with novel gas adsorption characteristics

Supporting Information. Simple Bacterial Detection and High-Throughput Drug Screening. Based on Graphene-Enzyme Complex

PREPARATION, CHARACTERISATION AND PHOTOCATALYTIC ACTIVITY OF TERNARY GRAPHENE-Fe 3 O 4 :TiO 2 NANOCOMPOSITES

Supporting information

Supporting Information:

Vertical Alignment of Reduced Graphene Oxide/Fe-oxide Hybrids Using the Magneto-Evaporation Method

Electronic Supplementary Information

Sonochemical Degradation of N-Methylpyrrolidone and Its Influence on Single Walled Carbon Nanotube Dispersion

Chemical functionalization of graphene sheets by solvothermal reduction of suspension of

In situ formation of metal Cd x Zn 1-x S nanocrystals on graphene surface: A novel method to synthesis sulfide-graphene nanocomposites

Functionalization of Graphene by Electrophilic Alkylation of Reduced Graphite

Reductive Arylation of Graphene: Insights into a Reversible Carbon Allotrope Functionalization Reaction

Characterization of partially reduced graphene oxide as room

Enhanced Electrochemical Catalytic Activity by Copper Oxide Grown on Nitrogen-doped Reduced Graphene Oxide

Instantaneous reduction of graphene oxide at room temperature

Supporting Information

Please do not adjust margins. New Approach for the Reduction of Graphene Oxide with Triphenylphosphine Dihalide

Electronic Supplementary Information

Supporting Information

Graphene oxide as acid catalyst for the room temperature. ring opening of epoxides

Graphene oxide was synthesized from graphite using the MH (modified Hummer s method) 30 and

Real-Time, In Situ Monitoring of the Oxidation of Graphite: Lessons Learned

--> Buy True-PDF --> Auto-delivered in 0~10 minutes. GB Translated English of Chinese Standard: GB5009.

Supplementary Material

Electronic Supporting Information

Supporting Information

Understanding Aqueous Dispersibility of Graphene Oxide and Reduced Graphene Oxide through pka Measurements

Optical Science of Nano-graphene (graphene oxide and graphene quantum dot) Introduction of optical properties of nano-carbon materials

Supporting Information

Synthesis of 2 ) Structures by Small Molecule-Assisted Nucleation for Plasmon-Enhanced Photocatalytic Activity

Enhanced Cr(VI) removal using iron nanoparticle decorated graphene

Supporting Information for: Inkjet Printing of High Conductivity, Flexible Graphene Patterns

SUPPLEMENTARY INFORMATION

Electronic Supplementary Information

Capacitive Behavior of Azide Functionalized Graphene Oxide as Electrode Materials

Supporting Information. Capping Nanoparticles with Graphene Quantum Dots for Enhanced Thermoelectric Performance

Electronic Supplementary Information. Noninvasive Functionalization of Polymers of Intrinsic Microporosity for Enhanced CO 2 Capture

Supporting Information

A Biosensor for the Detection of Single Base Mismatches in microrna

Three-dimensional Multi-recognition Flexible Wearable

Rapid dehalogenation of pesticides and organics at the interface of reduced. graphene oxide-silver nanocomposite

Electronic Supplementary Information

Electronic Supplementary information (ESI) Nanodiamonds as Metal-Free Catalyst. 5 Few-Layer Graphene-Graphene Oxide Composite containing

Supporting Information

Supplementary Material (ESI) for CrystEngComm. An ideal metal-organic rhombic dodecahedron for highly efficient

Driving forces for the self-assembly of graphene oxide on organic monolayers

Supporting Information

SUPPORTING INFORMATION

Supplementary information for:

Amphiphilic diselenide-containing supramolecular polymers

Mechanically Strong and Highly Conductive Graphene Aerogels and Its Use as. Electrodes for Electrochemical Power Sources

Supporting Information

Electronic Supplementary Information

Supplementary Information

A project report on SYNTHESIS AND CHARACTERISATION OF COPPER NANOPARTICLE-GRAPHENE COMPOSITE. Submitted by Arun Kumar Yelshetty Roll no 410 CY 5066

Probing the Kinetics of Ligand Exchange on Colloidal Gold. Nanoparticles by Surface-Enhanced Raman Scattering

A biphasic oxidation of alcohols to aldehydes and ketones using a simplified packed-bed microreactor

Supporting Information

Electronic Supplementary Information

Effects of interaction of electron-donor and accepter molecules on the electronic structure of graphene

*Corresponding author. Tel.: , ; fax: ; Materials and Method 2. Preparation of GO nanosheets 3

Tianyang Li, Yi-Hsin Liu, Basant Chitara and Joshua E. Goldberger*

Supporting Information

Electronic Supplementary Information. Facile Synthesis of Germanium-Graphene Nanocomposites. and Their Application as Anode Material for Lithium Ion

J. Am. Chem. Soc. 2009, 131,

Electronic Supplementary Information

Figure S-2. The high resolution XPS spectra of C 1s with corresponding fitting.

SUPPORTING INFORMATION. A New Approach for the Surface Enhanced Resonance Raman Scattering (SERRS)

Unless otherwise specified, reagents were used as received without further purification. FeCl 3

Supporting Information

Electronic Supporting Information for

Higher Chemistry PPA Questions Unit 1 PPA1 Effect of Concentration Changes On Reaction Rate Unit 1 PPA2 Effect of Temperature On Reaction Rate

Supporting Information

In Situ synthesis of architecture for Strong Light-Matter Interactions

Supplementary methods

Supplementary information. Derivatization and Interlaminar Debonding of Graphite-Iron Nanoparticles Hybrid

The sacrificial role of graphene oxide in stabilising Fenton-like catalyst GO Fe 3 O 4

Electronic Supplementary Information

O-Allylation of phenols with allylic acetates in aqueous medium using a magnetically separable catalytic system

Supporting Information Acid loaded porphyrin-based metal-organic framework for ammonia uptake

Platinum nanoparticles in suspension are as efficient as Karstedt s catalyst for alkene hydrosilylation

One-pot, green, rapid synthesis of flower-like gold. nanoparticles/reduced graphene oxide with. regenerated silk fibroin as efficient oxygen reduction

Recovery of Copper Renee Y. Becker Manatee Community College

Transcription:

Graphene Oxide: Stable Carbon Framework for Functionalization Siegfried Eigler,* a Stefan Grimm, a Ferdinand Hof, a Andreas Hirsch a a Department of Chemistry and Pharmacy and Institute of Advanced Materials and Processes (ZMP), Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Dr.-Mack Str. 81,90762 Fürth, Germany. Fax: +49 (0)911 6507865015; Tel: +49 (0)911 6507865005; E-mail: siegfried.eigler@zmp.unierlangen.de Experimental Section: Natural flake graphite was obtained from Asbury Carbon. The grade used was 3061. Potassium permanganate, sodium nitrate, sulfuric acid, hydriodic acid and trifluoroacetic acid were obtained from Sigma-Aldrich. Freeze-drying was accomplished on an ALPHA 1-4 LDplus from Matrtin Christ, Germany. For centrifugation a Sigma 4K15 centrifuge, Sigma Laborzentrifugen GmbH, Germany, was used. Elemental analysis was performed by combustion and gas chromatographic analysis with a VarioMicro CHNS analyzer from Elementar Analysensysteme GmbH, Hanau, Germany. Langmuir- Blodgett films were prepared using Langmuir-Blodgett Minitrough from KSV NIMA and films are prepared from MeOH/water mixtures on water as subphase at a pressure of 1.5 mn/m to yield slightly over packed films. These films were used for AFM imaging and scanning Raman spectroscopy. Thermogravimetric analysis (TGA) equipped with a mass spectrometer (MS) was accomplished on a Pyris 1 TGA equipped with Clarus SQ 8 C mass spectrometer with the following programmed time dependent temperature profile: RT-700 C (TGA-MS) with 10 K/min gradient, and cooling to RT. The initial sample weights were about 1.5 mg and the whole experiment was accomplished under inert gas atmosphere with a N 2 gas flow of 70 ml/min. Bruker Tensor FTIR spectrometer equipped with ZnSe was used for the measurements of GO films. UV/Vis spectroscopy was performed using Lamda 1050 from Perkin Elmer. Preparation of GO: The method for preparation is adopted from an earlier publication. 1 No pre-treatment of graphite was applied. Graphite (1 g, 83 mmol grade 3061, Asbury Carbon) and sodium nitrate (0.5 g, 5.9 mmol) were dispersed in concentrated sulphuric acid (24 ml). The dispersion was cooled to about 0 C. After that, over a period of three hours potassium permanganate (3.0 g, 19 mmol) was added. The temperature of the reaction mixture was kept below 10 C and stirred

for an additional 16 h. The reaction mixture was still cooled and during cooling diluted sulphuric acid (20 ml, 10 %) was continuously added to the reaction mixture over 2 h. After that water was added (60 ml, 6 h) and the temperature of the reaction mixture was kept below 10 C. The reaction mixture was then poured on ice (500 ml) and hydrogen peroxide (20 ml, 3 %) was added drop wise until gas evolution was completed, and the temperature was kept below 10 C. The obtained graphite oxide was purified by repeated centrifugation and dispersion in cooled water (below 10 C) until the ph of the supernatant was neutral. Finally, GO was yielded by mild sonication using a bath sonicator. Even without sonication, graphite oxide exfoliated to GO in some extent. The suspension was finally centrifuged three times at 5,000g to remove remaining graphite oxide. Elemental Analysis: C 45.68, H 2.28, N 0.03, S 3.62. Total weight loss according to thermogravimetric analysis (N 2, 25-700 C): 51.0 %; yield: 750 mg freeze dried. Preparation of GO-HCl: Freeze-dried GO (100 mg) was dispersed in water (100 ml) and sonicated using a cup-horn sonicator (30 W, pulsed 1s on, 1s off, 30 s). After sonication the dispersion was centrifuged at (10000g, 20 min) to remove minor amounts of few layered GO. The GO was further washed by water using a centrifuge (20000g, 1 h) for five times. The centrifuged GO was dispersed in hydrochloric acid (0.1 M) and centrifuged (20000g, 1 h). The contact time of acid with GO was kept about 30 min including 20 min centrifugation time. The GO was further washed by water using a centrifuge (20000g, 1 h) for five times. Totally this procedure took about 10 h. Finally, the GO solution was freeze-dried to yield a brownish/greenish fluffy felt that was stored in the fridge at 5 C. Elemental Analysis: C 44.86, H 2.72, N 0.03, S 3.45. Total weight loss according to thermogravimetric analysis (N 2, 25-700 C): 51.0 %. For reference and probing the stability of GO against HCl the procedure was repeated using HCl (1 M) yielding GO-HCl-2. Elemental Analysis: C 44.80, H 2.68, N 0.03, S 3.44. Total weight loss according to thermogravimetric analysis (N 2, 25-700 C): 55.0 %. Preparation of GO-NaOH: The method for preparation is adopted from an earlier publication. 2 Freeze-dried GO (100 mg) was dispersed in water (100 ml) and sonicated using a cup-horn sonicator (30 W, pulsed 1s on, 1s off, 30 s). After sonication the dispersion was centrifuged at (10000g, 20 min) to remove minor amounts of few layered GO. The GO was further washed by water using a centrifuge

(20000g, 1 h) for five times. The centrifuged GO was dispersed in sodium hydroxide solution (0.1 M) and centrifuged (20000g, 1 h). The contact time of base with GO was kept about 30 min including 20 min centrifugation time to avoid decomposition reactions. The GO was further washed by water using a centrifuge (20000g, 1 h) for five times. Totally this procedure took about 10 h. Finally, the GO solution was freeze-dried to yield a brownish fluffy felt that was stored in the fridge at 5 C. Elemental Analysis: C 43.38, H 2.95, N 0.08, S 1.53. Total weight loss according to thermogravimetric analysis (N 2, 25-700 C): 48.0 %. Treated samples at 40 C: Procedures for GO-NaOH and GO-HCl were repeated and a dispersion of GO (1 mg/ml) was prepared. Each dispersion was stored at 40 C for 16 h and purified afterwards, as described above. Results from elemental analysis are summarized in Table S1. The samples are labeled GO-40, GO-HCl-40 and GO-NaOH-40. GO-40: Elemental Analysis: C 42.11, H 2.86, N 0.12, S 1.16; Total weight loss according to thermogravimetric analysis (N 2, 25-700 C): 52.0 %. GO-HCl-40: Elemental Analysis: C 44.11, H 3.04, N 0.21, S 0.41; Total weight loss according to thermogravimetric analysis (N 2, 25-700 C): 49.0 %. GO-NaOH-40: Elemental Analysis: C 44.60, H 2.71, N 0.15, S 1.10; Total weight loss according to thermogravimetric analysis (N 2, 25-700 C): 47.0 %. Reduction of Langmuir-Blodgett films on Si/SiO 2 wafers: The wafers were paced in a vial on glass wool and some drops of hydriodic acid (57% in water) were placed on the glass wool. After that some drops of trifluoro acetic acid were dropped on the glass wool also. The vial was closed and after five minutes at room temperature the vial was heated to 80 C for an additional 10 minutes. After that the wafers were rinsed with water and dried at 80 C.

Figure S1. left: UV-Vis spectra of GO, GO-NaOH and GO-HCl (treated with 0.1M HCl; normalized on absorption at 235 nm) and right: UV-Vis spectra of GO-40, GO-NaOH-40 and GO-HCl-40: There are two transitions visible in all spectra. The first at 235 nm is due to π-π* transitions that were assigned C-C and C=C sp 2 hybrid regions. The shoulder at about 300 nm was described as n- π* transition and was assigned to C=O in sp 3 hybrid regions. 3, 4

Figure S2. FTIR spectra of GO, GO-HCl and GO-NaOH and GO-40, GO-HCl-40 and GO-NaOH-40; A) and B) overview of GO samples treated at 10 C or 40 C and C and D) enlargement of the fingerprint region (1800-900 cm -1 ) of GO samples treated at 10 C or 40 C.

Figure S3. TG-MS analysis of left: GO (black), GO-HCl (treated GO with 0.1M HCl, green) and GO- HCl (treated GO with 1M HCl, green dashed line) and GO-NaOH (blue); right: GO-40 (black), GO- HCl-40 (green) and GO-NaOH-40 (blue); numbers correlate to the remaining weight; the main weightloss is due to the decomposition of hydroxy groups and epoxy groups up to about 200 C; the weightloss step between 200 and 300 C originates from the decomposition of organosulfate as described earlier. 2, 5 Table S1. Elemental analyses of GO, GO-HCl, GO-HCl-2 GO-NaOH, GO-40, GO-HCl-40 and GO- NaOH-40 Sample C (%) H (%) N (%) S (%) GO 45.68 2.28 0.03 3.62 GO-HCl 44.86 2.72 0.03 3.45 GO-HCl-2 44.80 2.68 0.03 3.44 GO-NaOH 43.38 2.95 0.08 1.53 GO-40 42.11 2.86 0.12 1.16 GO-HCl-40 44.11 3.04 0.21 0.41 GO-NaOH-40 44.60 2.71 0.15 1.10

Figure S4. AFM images of reduced GO (rgo), rgo-hcl and rgo-naoh on Si/SiO 2 substrates with height-profiles below. Figure S5. AFM images of rgo-40, rgo-hcl-40 and rgo-naoh-40 on Si/SiO 2 substrates with height-profiles below.

Figure S6. Typical Raman spectra of rgo; left: mean quality of spectra (rgo, rgo-hcl, rgo-naoh, rgo-40, rgo-hcl-40 and middle: Raman spectrum of high-quality flakes; right: Raman spectra of rgo-naoh-40; mean quality with Γ 2D =130 cm -1 and highest quality with Γ 2D =52 cm -1. 1. S. Eigler, M. Enzelberger-Heim, S. Grimm, P. Hofmann, W. Kroener, A. Geworski, C. Dotzer, M. Rockert, J. Xiao, C. Papp, O. Lytken, H. P. Steinruck, P. Muller and A. Hirsch, Adv. Mater., 2013, 25, 3583-3587. 2. S. Eigler, C. Dotzer, F. Hof, W. Bauer and A. Hirsch, Chem. Eur. J., 2013, 19, 9490-9496. 3. Z. Luo, Y. Lu, L. A. Somers and A. T. C. Johnson, J. Am. Chem. Soc., 2009, 131, 898-899. 4. G. Eda, Y. Y. Lin, C. Mattevi, H. Yamaguchi, H. A. Chen, I. S. Chen, C. W. Chen and M. Chhowalla, Adv. Mater., 2010, 22, 505-509. 5. S. Eigler, C. Dotzer, A. Hirsch, M. Enzelberger and P. Müller, Chem. Mater., 2012, 24, 1276-1282.