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Investigation Into the Re-Arrangement of Copper Foams Pre- and Post-CO2 Electrocatalysis
Article Investigation into the Re-Arrangement of Copper Foams Pre- and Post-CO2 Electrocatalysis Jennifer A. Rudd 1 , Sandra Hernandez-Aldave 1 , Ewa Kazimierska 1, Louise B. Hamdy 1 , Odin J. E. Bain 1, Andrew R. Barron 1,2,3,4 and Enrico Andreoli 1,* 1 Energy Safety Research Institute, Swansea University, Bay Campus, Swansea SA1 8EN, UK; [email protected] (J.A.R.); [email protected] (S.H.-A.); [email protected] (E.K.); [email protected] (L.B.H.); [email protected] (O.J.E.B.); [email protected] (A.R.B.) 2 Department of Chemistry, Rice University, Houston, TX 77007, USA 3 Department of Materials Science and Nanoengineering, Rice University, Houston, TX 77007, USA 4 Faculty of Engineering, Universiti Teknologi Brunei, Jalan Tungku Link, Gadong BE1410, Brunei * Correspondence: [email protected] Abstract: The utilization of carbon dioxide is a major incentive for the growing field of carbon capture. Carbon dioxide could be an abundant building block to generate higher-value chemical products. Herein, we fabricated a porous copper electrode capable of catalyzing the reduction of carbon dioxide into higher-value products, such as ethylene, ethanol and propanol. We investigated the formation of the foams under different conditions, not only analyzing their morphological and Citation: Rudd, J.A.; crystal structure, but also documenting their performance as a catalyst. In particular, we studied Hernandez-Aldave, S.; Kazimierska, the response of the foams to CO2 electrolysis, including the effect of urea as a potential additive to E.; Hamdy, L.B.; Bain, O.J.E.; Barron, enhance CO catalysis. -
Closed Network Growth of Fullerenes
ARTICLE Received 9 Jan 2012 | Accepted 18 Apr 2012 | Published 22 May 2012 DOI: 10.1038/ncomms1853 Closed network growth of fullerenes Paul W. Dunk1, Nathan K. Kaiser2, Christopher L. Hendrickson1,2, John P. Quinn2, Christopher P. Ewels3, Yusuke Nakanishi4, Yuki Sasaki4, Hisanori Shinohara4, Alan G. Marshall1,2 & Harold W. Kroto1 Tremendous advances in nanoscience have been made since the discovery of the fullerenes; however, the formation of these carbon-caged nanomaterials still remains a mystery. Here we reveal that fullerenes self-assemble through a closed network growth mechanism by incorporation of atomic carbon and C2. The growth processes have been elucidated through experiments that probe direct growth of fullerenes upon exposure to carbon vapour, analysed by state-of-the-art Fourier transform ion cyclotron resonance mass spectrometry. Our results shed new light on the fundamental processes that govern self-assembly of carbon networks, and the processes that we reveal in this study of fullerene growth are likely be involved in the formation of other carbon nanostructures from carbon vapour, such as nanotubes and graphene. Further, the results should be of importance for illuminating astrophysical processes near carbon stars or supernovae that result in C60 formation throughout the Universe. 1 Department of Chemistry and Biochemistry, Florida State University, 95 Chieftan Way, Tallahassee, Florida 32306, USA. 2 Ion Cyclotron Resonance Program, National High Magnetic Field Laboratory, Florida State University, 1800 East Paul Dirac Drive, Tallahassee, Florida 32310, USA. 3 Institut des Matériaux Jean Rouxel, CNRS UMR 6502, Université de Nantes, BP32229 Nantes, France. 4 Department of Chemistry and Institute for Advanced Research, Nagoya University, Nagoya 464-8602, Japan. -
A Post-Buckminsterfullerene View of Carbon Chemistry
A POST-BUCKMINSTERFULLERENE VIEW OF CARBON CHEMISTRY Harold Kroto School of Chemistry and Molecular Sciences, University of Sussex, Brighton, BNI 9QJ UK Keywords: Cs0, Fullerenes, carbon particles INTRODUCTION The discovery of c60 Buckminsterfullerene, Fig 1, has its origins in a research programme involving synthetic chemistry, microwave spectroscopy and radioastronomyl. In 1915, at Sussex (with David Walton), the long chain polyyne H-CeC-CsC-CsN was synthesised and studied by microwave spectroscopy. Subsequently, with Takeshi Oka and NRC(0ttawa) astronomers, the molecule was discovered in space, Fig 2, by radioastronomy using the laboratory microwave frequencies. This discovery led on to the detection of the even longer carbon chain molecules HCTN, HCgN and HCl.lN in the space between the stars2. Further work aimed at understanding the formation of the chains in space focussed attention on the possibility that they are produced at the same time as carbon dust in red giant stars1,*. During experiments at Rice University in 1985 (with James Heath, Sean O'Brien, Robert Curl and Richard Smalley), designed to simulate the conditions in these stars and explore their capacity for carbon chain formation, the exciting discovery that C60 was remarkably stable was made3. It was found that under conditions where almost all the atoms in a carbon plasma had nucleated to form microparticles the molecule c60 remained behind - together with some CTO. This result was, as is now well 'known, rationalised on the basis of the closed cage structure shown in Fig 1. It was proposed that the geodesic and aromatic factors inherent in such a structure could account for the stability of the molecule. -
Metallofullerene and Fullerene Formation from Condensing Carbon Gas Under Conditions of Stellar Outflows and Implication to Star
Metallofullerene and fullerene formation from condensing carbon gas under conditions of stellar outflows and implication to stardust Paul W. Dunka,b,1, Jean-Joseph Adjizianc, Nathan K. Kaiserb, John P. Quinnb, Gregory T. Blakneyb, Christopher P. Ewelsc,1, Alan G. Marshalla,b,1, and Harold W. Krotoa,1 aDepartment of Chemistry and Biochemistry, Florida State University, Tallahassee, FL 32306; bIon Cyclotron Resonance Program, National High Magnetic Field Laboratory, Florida State University, Tallahassee, FL 32310; and cInstitut des Matériaux Jean Rouxel, Centre National de la Recherche Scientifique, Unité Mixte de Recherche 6502, Université de Nantes, BP 32229 Nantes, France Contributed by Harold W. Kroto, August 29, 2013 (sent for review June 13, 2013) Carbonaceous presolar grains of supernovae origin have long confirmed to exist in circumstellar and interstellar environments. been isolated and are determined to be the carrier of anomalous C60 and C70 were first unequivocally detected in a planetary 22Ne in ancient meteorites. That exotic 22Ne is, in fact, the decay nebula in 2010, which was thought to be hydrogen deficient (11). isotope of relatively short-lived 22Na formed by explosive nucleo- Thereafter, Buckminsterfullerene was detected in hydrogen- synthesis, and therefore, a selective and rapid Na physical trapping rich [including the least H-deficient R Coronae Borealis stars] mechanism must take place during carbon condensation in super- (12, 13) and oxygen-rich environments (14), as well as the ISM nova ejecta. Elucidation of the processes that trap Na and produce (15) and a protoplanetary nebula (16). Moreover, fullerenes large carbon molecules should yield insight into carbon stardust have been detected in a host of other circumstellar and in- enrichment and formation. -
Formation of Buckminsterfullerene (C60) in Interstellar Space
Formation of buckminsterfullerene ( ) C60 in interstellar space Olivier Berné1 and A. G. G. M. Tielens Leiden Observatory, Leiden University, P.O. Box 9513, NL- 2300 RA Leiden, The Netherlands Edited by Neta A. Bahcall, Princeton University, Princeton, NJ, and approved November 2, 2011 (received for review August 31, 2011) Buckminsterfullerene (C60) was recently confirmed as the largest region, at high angular resolution (Fig. 1). This measurement can molecule identified in space. However, it remains unclear how be used to derive the integrated intensity radiated by the nebula, and where this molecule is formed. It is generally believed that which can be used as a calibrator, to convert the Spitzer observa- C60 is formed from the buildup of small carbonaceous compounds tions of the PAHs and C60 bands into absolute chemical abun- in the hot and dense envelopes of evolved stars. Analyzing infrared dances of these species, allowing a quantitive study of PAH and observations, obtained by Spitzer and Herschel, we found that C60 C60 chemical evolution. is efficiently formed in the tenuous and cold environment of an interstellar cloud illuminated by strong ultraviolet (UV) radiation Measurement of the Far Infrared Integrated Intensity of Dust Emission I fields. This implies that another formation pathway, efficient at in the Nebula. The far infrared integrated intensity FIR was ex- low densities, must exist. Based on recent laboratory and theore- tracted by fitting the spectral energy distribution (SED) at each tical studies, we argue that polycyclic aromatic hydrocarbons are position in the cross-cut shown in Fig. 1. For these positions, we converted into graphene, and subsequently C60, under UV irradia- have used the brightnesses as measured by Herschel Photodetec- tion from massive stars. -
Reactions of Graphene Oxide and Buckminsterfullerene in the Aquatic Environment Yingcan Zhao Purdue University
Purdue University Purdue e-Pubs Open Access Dissertations Theses and Dissertations 8-2016 Reactions of graphene oxide and buckminsterfullerene in the aquatic environment Yingcan Zhao Purdue University Follow this and additional works at: https://docs.lib.purdue.edu/open_access_dissertations Part of the Environmental Engineering Commons Recommended Citation Zhao, Yingcan, "Reactions of graphene oxide and buckminsterfullerene in the aquatic environment" (2016). Open Access Dissertations. 896. https://docs.lib.purdue.edu/open_access_dissertations/896 This document has been made available through Purdue e-Pubs, a service of the Purdue University Libraries. Please contact [email protected] for additional information. Graduate School Form 30 Updated PURDUE UNIVERSITY GRADUATE SCHOOL Thesis/Dissertation Acceptance This is to certify that the thesis/dissertation prepared By Yingcan Zhao Entitled REACTIONS OF GRAPHENE OXIDE AND BUCKMINSTERFULLERENE IN THE AQUATIC ENVIRONMENT For the degree of Doctor of Philosophy Is approved by the final examining committee: Chad T. Jafvert Chair Timothy R. Filley Inez Hua Ronald F. Turco To the best of my knowledge and as understood by the student in the Thesis/Dissertation Agreement, Publication Delay, and Certification Disclaimer (Graduate School Form 32), this thesis/dissertation adheres to the provisions of Purdue University’s “Policy of Integrity in Research” and the use of copyright material. Approved by Major Professor(s): Chad T. Jafvert Approved by: Dulcy M. Abraham 6/21/2016 Head of the Departmental Graduate Program Date i REACTIONS OF GRAPHENE OXIDE AND BUCKMINSTERFULLERENE IN THE AQUATIC ENVIRONMENT A Dissertation Submitted to the Faculty of Purdue University by Yingcan Zhao In Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy August 2016 Purdue University West Lafayette, Indiana ii To my parents and Liang, for their love, support and encouragement. -
From Quantum Mechanics to Nanoparticles and Their Applications
Part 2 Learning Station XIa: From quantum mechanics to nanoparticles and their applications Quantum Spin-Off 2 LEARNING STATION XIa: FROM QUANTUM MECHANICS TO NANOPARTICLES AND THEIR APPLICATIONS Introduction ..................................................................................................................................................... 3 1. Elementary particles in nanotechnology ...................................................................................................... 3 2. Size matters .................................................................................................................................................. 4 3. Can we observe this phenomenon in a real-life experiment? ....................................................................... 4 3.a Emission spectrum of single atoms............................................................................................................... 4 3.b How can we observe the emission spectrum? ............................................................................................. 5 3.c Step-by-step instructions to make your own spectrometer ......................................................................... 5 3.d What can we observe and investigate with our spectrometer?................................................................... 9 3.e How does fluorescence spectrometry work? ............................................................................................... 9 4. Quantum dots ............................................................................................................................................. -
Nanostructure Quantification of Carbon Blacks
Journal of C Carbon Research Article Nanostructure Quantification of Carbon Blacks Madhu Singh and Randy L. Vander Wal * John and Willie Leone Family Department of Energy and Mineral Engineering and the Earth and Mineral Sciences (EMS) Energy Institute, Penn State University, University Park, State College, PA 16802, USA; [email protected] * Correspondence: [email protected]; Tel.: +1-814-865-5813 Received: 20 November 2018; Accepted: 21 December 2018; Published: 31 December 2018 Abstract: Carbon blacks are an extensively used manufactured product. There exist different grades by which the carbon black is classified, based on its purpose and end use. Different properties inherent to the various carbon black types are a result of their production processes. Based on the combustion condition and fuel used, each process results in a carbon black separate from those obtained from other processes. These carbons differ in their aggregate morphology, particle size, and particle nanostructure. Nanostructure is key in determining the material’s behavior in bulk form. A variety of carbon blacks have been analyzed and quantified for their lattice parameters and structure at the nanometer scale, using transmission electron microscopy and custom-developed fringe analysis algorithms, to illustrate differences in nanostructure and their potential relation to observed material properties. Keywords: carbon; nanostructure; HRTEM; fringe; quantification 1. Introduction Carbon black is manufactured elemental carbon with customized particle size and aggregate morphology [1]. Produced from the partial combustion or thermal decomposition of hydrocarbons, carbon black is an engineered material, primarily composed of >98% elemental carbon. This number may vary based on its production process and final desired application, where carbon black may be doped with other elements like oxygen, nitrogen, or sulfur to impart solubility, better dispersion or binding properties to the material. -
Production and Functionalization of Cobalt Nanofoams for Energy Storage Energy Engineering and Management
Production and functionalization of cobalt nanofoams for energy storage Naureen Khanam Thesis to obtain the Master of Science Degree in Energy Engineering and Management Supervisors: Prof. Maria de Fátima Grilo da Costa Montemor Prof. Maria Teresa Oliveira de Moura e Silva Examination Committee Chairperson: Duarte de Mesquita e Sousa Supervisor: Prof. Maria Teresa Oliveira de Moura e Silva Members of the Committee: Prof. Raquel Alexandra Galamba Duarte Dr. Alberto Adán Más October 2019 I declare that this document is an original work of my own authorship and that it fulfils all the requirements of the Code of Conduct and Good Practices of the Universidade de Lisboa. ii Acknowledgements Acknowledgements All praise to the Almighty, the Most Merciful. I would like to express gratitude to my supervisors Professor Fátima Montemor and Professor Maria Terresa Moura e Silva for their continuous guidance, advices and support during this work. My heartful gratitude to Dr. Alberto Adán Más for his support and all the endeavours to teach me everything from zero. I would like to thank EIT KIC InnoEnergy for providing scholarship under CFAFE program for my master study. This research work was developed under IDI&CA/SuperStore 0712045/ISEL project funded by Instituto Politécnico de Lisboa. I would like to thank this institution for offering me the scientific initiation fellowship under this project. I appreciate all the support of my colleagues for their help, support and kindness throughout this master study in two different countries. Finally, respect and love for my family and friends who helped keeping my moral spirit high during this journey from thousand miles apart. -
Diatomic Carbon Measurements with Laser-Induced Breakdown Spectroscopy
University of Tennessee, Knoxville TRACE: Tennessee Research and Creative Exchange Masters Theses Graduate School 5-2015 Diatomic Carbon Measurements with Laser-Induced Breakdown Spectroscopy Michael Jonathan Witte University of Tennessee - Knoxville, [email protected] Follow this and additional works at: https://trace.tennessee.edu/utk_gradthes Part of the Atomic, Molecular and Optical Physics Commons, and the Plasma and Beam Physics Commons Recommended Citation Witte, Michael Jonathan, "Diatomic Carbon Measurements with Laser-Induced Breakdown Spectroscopy. " Master's Thesis, University of Tennessee, 2015. https://trace.tennessee.edu/utk_gradthes/3423 This Thesis is brought to you for free and open access by the Graduate School at TRACE: Tennessee Research and Creative Exchange. It has been accepted for inclusion in Masters Theses by an authorized administrator of TRACE: Tennessee Research and Creative Exchange. For more information, please contact [email protected]. To the Graduate Council: I am submitting herewith a thesis written by Michael Jonathan Witte entitled "Diatomic Carbon Measurements with Laser-Induced Breakdown Spectroscopy." I have examined the final electronic copy of this thesis for form and content and recommend that it be accepted in partial fulfillment of the equirr ements for the degree of Master of Science, with a major in Physics. Christian G. Parigger, Major Professor We have read this thesis and recommend its acceptance: Horace Crater, Joseph Majdalani Accepted for the Council: Carolyn R. Hodges Vice Provost and Dean of the Graduate School (Original signatures are on file with official studentecor r ds.) Diatomic Carbon Measurements with Laser-Induced Breakdown Spectroscopy A Thesis Presented for the Master of Science Degree The University of Tennessee, Knoxville Michael Jonathan Witte May 2015 c by Michael Jonathan Witte, 2015 All Rights Reserved. -
Studies of Cobalt and Iron Oxides/ Oxyhydroxides Nanostructures for Electrochemical Applications
STUDIES OF COBALT AND IRON OXIDES/ OXYHYDROXIDES NANOSTRUCTURES FOR ELECTROCHEMICAL APPLICATIONS LEE KIAN KEAT NATIONAL UNIVERSITY OF SINGAPORE 2014 STUDIES OF COBALT AND IRON OXIDES/ OXYHYDROXIDES NANOSTRUCTURES FOR ELECTROCHEMICAL APPLICATIONS LEE KIAN KEAT (M. Sc., Universiti Teknologi Malaysia) A THESIS SUBMITTED FOR THE DEGREE OF DOCTOR OF PHILOSOPHY DEPARTMENT OF CHEMISTRY NATIONAL UNIVERSITY OF SINGAPORE 2014 DECLARATION I hereby declare that the thesis is my original work and it has been written by me in its entirely, under the supervision of Assoc. Prof. Sow Chorng Haur (Department of Physics) and Assoc. Prof. Chin Wee Shong (Department of Chemistry), National University of Singapore, between 3 August 2009 and 31 Jan 2014. I have duly acknowledged all the sources of information which have been used in the thesis. This thesis has also not been submitted for any degree in any university previously. The content of the thesis has been partly published in: 1. Lee, K. K., Loh, P. Y., Sow, C. H., Chin, W. S. CoOOH nanosheet electrodes: Simple fabrication for sensitive electrochemical sensing of hydrogen peroxide and hydrazine. Biosensors and Bioelectronics, 2013, 39, 255-260. (Chapter 3 & 5) 2. Lee, K. K., Loh, P. Y., Sow, C. H., Chin, W. S. CoOOH nanosheets on cobalt substrate as a non-enzymatic glucose sensor. Electrochemistry Communications, 2012, 20, 128-132. (Chapter 4) 3. Lee, K. K.#, Deng, S.#, Fan, H. M., Mhaisalkar, S., Tan, H. R., Tok, E. S., Loh, K. P., Chin, W. S, Sow, C. H. α-Fe2O3 nanotubes-reduced graphene oxide composites as synergistic electrochemical capacitor materials. Nanoscale, 2012, 4, 2958-2961. -
Nanotechnology - Fundamentals and Applications 1
D. Cremer, CHEM 6342, Nanotechnology - Fundamentals and Applications 1 CHEM 6342 Nanotechnology – Fundamentals and Applications Class location: TBD Lectures, time and location: TBD Lab times and location: TBD Instructor: Dieter Cremer, 325 FOSC, ext 8-1300, [email protected] http://smu.edu/catco/ Office Hours: By appointment Units: 3 Grading: ABC Letter Grade Class number TBD 1. Rationale: Nanotechnology (NT) is a rather young discipline, which came up in the nineties. Nevertheless, NT has gained so much importance within the last years that universities at all rankings have introduced or are going to introduce NT teaching programs. Predictions say that NT will change our lives and society more than computer technology and electricity have done together. The course will provide an overview over NT. It will show that the nano regime is so different from other regimes because both classical and quantum effects can be active thus leading to unique properties of nano devices. NT is a highly interdisciplinary science, which will be reflected in the course by making reference to chemistry, physics, biology, pharmacy, and engineering. Applications of NT, as they are already in use today or as they are planned for the future, will be discussed. 2. Course Recommendations: The course is designed to reach all graduate students who had have an education in chemistry, physics, engineering or biology. It does not require special knowledge in mathematics or theoretical physics. The course contents will be presented in self-sustained modules, which make it possible to follow the course without special knowledge. The course will prepare for the interdisciplinary work in NT.