Relevant bibliographies by topics / Ultracold chemistry

Academic literature on the topic 'Ultracold chemistry'

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Published: 10 December 2022
Last updated: 28 January 2023

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Journal articles on the topic "Ultracold chemistry"

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Bell, Martin T., and Timothy P. Softley. "Ultracold molecules and ultracold chemistry." Molecular Physics 107, no. 2 (January 20, 2009): 99–132. http://dx.doi.org/10.1080/00268970902724955.

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Hutson, J. M. "Ultracold Chemistry." Science 327, no. 5967 (February 11, 2010): 788–89. http://dx.doi.org/10.1126/science.1186703.

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Balakrishnan, N., and A. Dalgarno. "Chemistry at ultracold temperatures." Chemical Physics Letters 341, no. 5-6 (June 2001): 652–56. http://dx.doi.org/10.1016/s0009-2614(01)00515-2.

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Pérez-Ríos, Jesús, Maxence Lepers, Romain Vexiau, Nadia Bouloufa-Maafa, and Olivier Dulieu. "Progress toward ultracold chemistry: ultracold atomic and photonic collisions." Journal of Physics: Conference Series 488, no. 1 (April 10, 2014): 012031. http://dx.doi.org/10.1088/1742-6596/488/1/012031.

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Cornish, Simon L., and Jeremy M. Hutson. "Toward a coherent ultracold chemistry." Science 375, no. 6584 (March 4, 2022): 975–76. http://dx.doi.org/10.1126/science.abn1053.

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Benka, Stephen G. "Ultracold chemistry in supersonic beams." Physics Today 65, no. 12 (December 2012): 21. http://dx.doi.org/10.1063/pt.3.1811.

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Saßmannshausen, Heiner, Johannes Deiglmayr, and Frédéric Merkt. "Exotic Chemistry with Ultracold Rydberg Atoms." CHIMIA International Journal for Chemistry 70, no. 4 (April 27, 2016): 263–67. http://dx.doi.org/10.2533/chimia.2016.263.

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Richter, Florian, Daniel Becker, Cédric Bény, Torben A. Schulze, Silke Ospelkaus, and Tobias J. Osborne. "Ultracold chemistry and its reaction kinetics." New Journal of Physics 17, no. 5 (May 7, 2015): 055005. http://dx.doi.org/10.1088/1367-2630/17/5/055005.

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Liu, Yu, David D. Grimes, Ming-Guang Hu, and Kang-Kuen Ni. "Probing ultracold chemistry using ion spectrometry." Physical Chemistry Chemical Physics 22, no. 9 (2020): 4861–74. http://dx.doi.org/10.1039/c9cp07015j.

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Tennyson, Jonathan, Laura K. McKemmish, and Tom Rivlin. "Low-temperature chemistry using the R-matrix method." Faraday Discussions 195 (2016): 31–48. http://dx.doi.org/10.1039/c6fd00110f.

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Techniques for producing cold and ultracold molecules are enabling the study of chemical reactions and scattering at the quantum scattering limit, with only a few partial waves contributing to the incident channel, leading to the observation and even full control of state-to-state collisions in this regime. A new R-matrix formalism is presented for tackling problems involving low- and ultra-low energy collisions. This general formalism is particularly appropriate for slow collisions occurring on potential energy surfaces with deep wells. The many resonance states make such systems hard to treat theoretically but offer the best prospects for novel physics: resonances are already being widely used to control diatomic systems and should provide the route to steering ultracold reactions. Our R-matrix-based formalism builds on the progress made in variational calculations of molecular spectra by using these methods to provide wavefunctions for the whole system at short internuclear distances, (a regime known as the inner region). These wavefunctions are used to construct collision energy-dependent R-matrices which can then be propagated to give cross sections at each collision energy. The method is formulated for ultracold collision systems with differing numbers of atoms.
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Dissertations / Theses on the topic "Ultracold chemistry"

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Richter, Florian [Verfasser]. "Ultracold chemistry and its reaction kinetics / Florian Richter." Hannover : Technische Informationsbibliothek und Universitätsbibliothek Hannover (TIB), 2015. http://d-nb.info/1077017014/34.

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Wolf, Joschka [Verfasser]. "State-to-state chemistry with ultracold neutral Rb atoms / Joschka Wolf." Ulm : Universität Ulm, 2020. http://d-nb.info/1202515541/34.

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Blomdahl, Kajsa-My. "Numerical Calculations of Efimov States in Ultracold Atomic Systems." Thesis, KTH, Skolan för kemivetenskap (CHE), 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-207752.

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In systems of ultracold atoms,  the  quantum  Efimov  effect  can  appear where identical bosons form an infinite tower of bound trimer states in the resonant limit, at the bound dimer dissociation threshold. The most characteristic feature of this effect is that their energy spectrum obey a geometric scaling law, which is universal in the sense that it emerges irrespective of the nature of the two body forces. Using  a  model  potential,  constructed  to  resemble the two body interaction between alkali atoms,  which was  fine tuned to control the  scattering  length,  energy  eigenvalues  for  the  two-  and  threebody problem were calculated numerically. The results where  fitted  to  the analytic theory and the appearance of the first Efimov state was positioned at a scattering length of -9.23rvdW , which is in good  agreement  with  the universal value -9.2rvdW .
I system av ultrakalla atomer kan en kvanteffekt, kallad Efimoveffekt, uppkomma  där  identiska  bosoner  bildar  ett  oändligt  torn  av  bundna  trekroppstillstånd då spridningslängden går mot oändligheten, vid dissociationströskeln för en svagt bunden dimer.  Det mest utmärkande för denna effekt är att Efimovtillståndens energispektrum följer en geometrisk skalningslag, som är universell i den meningen att den framträder oberoende av hur atomernas parvisa växelverkan ser ut.  Med hjälp av en modellpotential som konstruerats för att efterlikna den parvisa växelverkan mellan två alkaliatomer finjusterades spridningslängden.  Energiegenvärdena för två- och tre-kropps problemen  beräknades  numeriskt  vid  olika  spridningslängder.   Resultaten jämfördes  med  den  analytiska  teorin  och  den  första  tre-kroppsresonansen uppkom  vid  spridningslängden  -9.23rvdW ,  vilket  överenstämmer  med  det experimentellt funna universella värdet -9.2rvdW .
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Enderlein, Martin [Verfasser], and Tobias [Akademischer Betreuer] Schätz. "Optical ion trapping for (scalable) quantum simulations and ultracold chemistry experiments = Optisches Ionenfangen für (skalierbare) Quantensimulationen und Ultrakalte-Chemie-Experimente." Freiburg : Universität, 2013. http://d-nb.info/1123474303/34.

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Doherty, William Gerard. "Cold atom production via the photo dissociation of small molecules." Thesis, University of Oxford, 2012. http://ora.ox.ac.uk/objects/uuid:523f87e0-3f19-4382-941c-74b06023b767.

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This thesis describes the development of a relatively novel technique for the gen- eration and subsequent trapping of cold species. Molecules in a pulsed supersonic expansion are photolysed, such that the centre-of-mass velocity vector of one of the fragments is equal in magnitude but opposed in orientation to the lab-frame velocity of the precursor molecule. This technique, known as ‘Photostop’, leaves a fraction of the fragments with a narrow velocity distribution, centered around zero velocity in the lab-frame. They can be shown to have zero velocity by changing the time between photodissociation and ionisation; fragments with a high kinetic energy will leave the ionisation volume prior to interrogation. The underlying velocity distribu- tion is uncovered by using the velocity-map imaging technique, and the temperature of the fragments can be determined. The method was originally optimised for the molecular case. Cold NO has been produced from the dissociation of NO₂ molecules, and a single rotational state has been shown to remain in the ionisation volume 10 μs after dissociation, implying a sample temperature of 1.17 K. Using the optimised experimental conditions de- rived from the velocity cancellation of NO, the atomic case is demonstrated for the dissociation of Br₂ to give zero-velocity Br fragments. The Br atoms are seen for delay times in excess of 100 μs, showing the greater applicability of the method to the atomic case. The temperature of the residual atoms is shown to be in the milliKelvin regime, as determined through detailed Monte Carlo simulation of the motion of the stopped atoms. The possibility of trapping the ultracold Br atoms in a magnetic field is explored, and a quadrupolar trap created between two per- manent bar magnets is demonstrated to confine the atoms spatially, within the ion extraction optics, for delays in excess of 1 ms. The Photostop technique is intended to be a stepping stone on the way to widening the number of chemical species available for study in the ultracold regime. The possibility of improvements to the experiment is considered, in order to increase the efficiency of the experiment such that the number density becomes high enough to be viable as a source of atoms for use in cold chemical reactive studies. The possibility of extending the method so as to be used as a tunable velocity source of atoms is also discussed.
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Harper, Lee D. "Stark deceleration and reactivity of polyatomic molecules and ions at low temperatures." Thesis, University of Oxford, 2013. http://ora.ox.ac.uk/objects/uuid:ac6b9303-3abe-4085-b9fc-6a3e76486619.

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This thesis describes the development of a new experimental technique for studying tunable-collision-energy, quantum state-selected, low-temperature ion-molecule reactions. This has been achieved through the combination of a Stark decelerator for neutral dipolar molecules, and a linear Paul ion trap. The Stark deceleration process for ND3 was examined in detail, through the analysis of experimental data in combination with newly written molecular dynamics simulation programs. In order to prepare a sample of molecules appropriate for collision studies, additional beamline components were introduced after the decelerator. These components were: two hexapoles, to provide transverse focussing, maximising the molecular density; a molecular buncher, providing increased longitudinal velocity resolution; and a fast-opening shutter, to separate decelerated molecules from undecelerated molecules. The sympathetic-cooling of Xe+ ions and ND+3 ions by laser-cooled, Coulomb crystallised 40Ca+ ions with the ion trap was also studied. In particular, the stable trapping of Xe+ was demonstrated for the first time, and the experimental developments that led to this are discussed. The work in this thesis represents significant progress towards studying the reaction of tunable-energy ND3 in the |j,mk> = |1,−1> quantum state with cold Xe+ ions. Ion-molecule reactions utilising ND3 molecules electrostatically guided through the Stark decelerator were performed. It was observed that the main source of error in these experiments was in the calculation of the initial number of Xe+ ions that had been sympathetically cooled into the Coulomb crystal. The sensitivity of the crystal morphology to the number of Xe+ ions was evaluated using molecular dynamics simulations. Strategies have been developed to reduce this uncertainty in future studies. In addition to experimental work, the theory of low temperature ion-molecule reactions has been developed further. The temperature at which classical and quantum mechanical calculations diverge due to purely statistical effects has been investigated using different model intermolecular potentials, for closed-shell and open-shell species, and in the ground and rotationally excited states. From the results of these calculations, several promising candidate reactions have been suggested that might exhibit statistical quantum behaviour at experimentally achievable temperatures.
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Deb, Nabanita. "Towards cold state-selected ion-molecule reactions." Thesis, University of Oxford, 2014. http://ora.ox.ac.uk/objects/uuid:1a3899d3-7476-49ac-8f4b-3c0e7a7e8680.

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In recent years there has been much progress in the field of cold and ultracold molecular physics and a variety of experimental techniques for producing cold matter now exist. In particular, the generation of trapped molecular ions at mK temperatures has been achieved by sympathetic-cooling with laser-cooled atomic ions. By implementing schemes to selectively prepare and control the internal quantum state of molecular ions, and developing detection techniques, it will be increasingly possible to study cold state-selected chemical collisions in an ion-trap. Most molecular species produced in a selected rovibrational state have a lifetime of a few seconds, before the population is redistributed across numerous rovibrational states by interaction with the ambient blackbody radiation (BBR). Consequently, the investigation of state-selected reaction dynamics at low temperatures in experiments where long time scales (minutes to hours) are required, is hindered. This thesis looks into developing strategies that maintain state selection in molecular ions, allowing one to observe state-selected reactions in cold environments, in particular the state-selected reaction between C2H+2 and ND3. Examining reactive ion molecule collisions under cold conditions provides insight into fundamental reaction dynamics, which are thermally averaged out at higher temperatures. A theoretical model is used to investigate laser-driven, blackbody-mediated, rotational cooling schemes for several 1Σ and 2Π diatomic species. The rotational cooling is particularly effective for DCl+ and HCl+, for which 92% and >99% (respectively) of the population can be driven into the rovibrational ground state. For the other systems a broadband optical pumping source is found to enhance the population that can be accumulated in the rovibrational ground state by up to 29% more than that achieved when exciting a single transition. The influence of the rotational constant, dipole moments and electronic state of the diatomics on the achievable rotational cooling is also studied. This approach is extended to consider the BBR interaction and rotational cooling of a linear polyatomic ion, C2H+2, which has a 2Π electronic ground state. The (1-0) band of the ν5 cis-bending mode is infrared active and strongly overlaps the 300 K blackbody spectrum. Hence the lifetimes of state-selected rotational levels are found to be short compared to the typical timescale of ion trapping experiments. Laser cooling schemes are proposed that could be experimentally viable, which involves simultaneous pumping of a set of closely spaced Q-branch transitions on the 2Δ5/2-2Π3/2 band together with two 2Σ+– 2Π1/2 lines. It is shown that this should lead to >70% of total population in the lowest rotational level at 300 K and over 99% at 77 K. In order to identify states of the acetylene ion that could be trapped sufficiently long enough for state-selected reactions in the ion trap with decelerated ND3, the theoretical work has been complemented by experimental investigations into the production of C2H+2 in selected states, and ion trapping of the same using sinusoidal and digital trapping voltages. Appropriate (2+1) REMPI (Resonance Enhanced Multiphoton Ionization) schemes are used to produce C2H+2 in different quantum states, with (1+1) Resonance Enhanced Multiphoton Dissociation (REMPD) employed to detect the ion thus produced. The concept of digital ion trapping for ejection onto MCPs is introduced. A comprehensive comparison between sinusoidal and digital trapping fields has been performed with respect to trap depth and stability regions. Programs have been developed to calculate the stability regions for different ions under varying experimental conditions. The trap depth has been derived for both digital and sinusoidal trapping fields. It is observed that as τ increases, the trap depth of a digital trap increases. For τ = 0.293, the trap depth and stability diagram for both sinusoidal and digital trapping fields would be equivalent. The trap depth at which the sinusoidal trap operates experimentally in our research group is ~1.36 eV. In contrast, the experimental parameters at which the digital trap operates generates a trap depth of 1.21 eV. Ca+ Coulomb crystals have been formed, stably trapped and stored for extended periods of time in both sinusoidally and digitally time-varying trapping fields. The sympathetic cooling of a diverse range of ions into Ca+ Coulomb crystals is demonstrated, again using both sinusoidal and digital trapping fields. Mass spectrometric detection of ionic reaction products using a novel ejection scheme has been developed, where ejection is achieved by switching off the trapping voltage and converting the quadrupole trap into an extractor-repeller pair by providing the ion trap electrodes with appropriate ejection pulses. This technique is developed using a digital trapping voltage rather than the sinusoidal trapping voltage, as ejection with sinusoidal trapping voltages is not clean (resonance circuitry used in the electronics induces ringing after switching off the trapping voltage). Coulomb crystals, both pure Ca+ and multi-component crystals, are ejected from the ion trap and the TOF trace obtained is recorded on an oscilloscope. When the integrated, base-line subtracted TOF peak is plotted against the number of ions in a Ca+ crystal and sympathetically-cooled Ca+ – CaF+ crystal, a linear relationship is obtained. This technique is found to be well mass-resolved, with the signal arising from CaOH+ (57 amu) and CaOD+ (58 amu) resolvable on the TOF trace. This technique would enable one to monitor a reaction in a Coulomb crystal where the reactant and product species are both either lighter or heavier than calcium, such as the reaction between C2H+2 and ND3, something which has not been previously possible. It is, also, potentially a very important technique for reactions with many product channels.
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Borsalino, Dimitri. "Molécules polaires ultra-froides : structure électronique et contrôle optique." Thesis, Paris 11, 2015. http://www.theses.fr/2015PA112232/document.

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Ce mémoire s’inscrit dans le cadre des recherches sur les molécules ultra-froides, en forte expansion depuis plusieurs années. Contrairement aux atomes, les molécules ne peuvent que très difficilement être refroidies par laser. Il est donc nécessaire d’explorer des méthodes alternatives pour parvenir à la création de gaz moléculaires ultra-froids. Ce travail théorique s’est focalisé sur une classe particulière de molécules diatomiques hétéronucléaires, présentant un moment dipolaire électrique ou magnétique intrinsèque à l’origine de leurs interactions mutuelles anisotropes.Sur la base de la connaissance précise de la spectroscopie des molécules KRb et KCs (présentant un moment dipolaire électrique intrinsèque notable), combinée à des résultats théoriques, nous avons modélisé le refroidissement de leurs degrés de liberté internes au moyen du passage adiabatique Raman stimulé (STIRAP), processus laser conduisant les molécules dans leur état fondamental absolu. Plusieurs schémas STIRAP ont été discutés et comparés entre eux du point de vue de leur efficacité.Nous avons ensuite étudié la molécule RbCa, dont la spectroscopie est encore inconnue. Cette espèce est caractérisée par la présence conjointe d’un moment dipolaire électrique et magnétique permanent, qui présente un fort intérêt pour les possibilités de contrôle des interactions anisotropes qu’ils engendrent. Nous avons déterminé la structure électronique de RbCa par deux méthodes différentes de chimie quantique, permettant ainsi de qualifier la précision des résultats. Nous avons aussi proposé un schéma de transitions laser conduisant à la formation de molécules froides de RbCa à partir des atomes séparés.La manipulation et le piégeage de molécules repose sur la connaissance de leur réponse à un champ électromagnétique externe, caractérisée par leur polarisabilité dipolaire dynamique. Les calculs de chimie quantique entrepris plus haut nous ayant permis d’accéder à des états moléculaires très excités, nous avons déterminé cette quantité pour toute une série de molécules diatomiques (dimères alcalins, RbCa, RbSr,…). Nous avons ainsi pu déterminer les paramètres optimaux pour le piégeage laser de ces molécules
This thesis deals with ultracold molecules research, which interest has been growing for several years. Unlike atoms, laser-cooling molecules is very difficult. Alternative methods are necessary to be searched for in order to create ultracold molecular gases. This theoretical work focuses on a particular type of heteronuclear diatomic molecules, possessing an intrinsic electric or magnetic dipole moment, from which originates their mutual anisotropic interactions.Based on the precise knowledge of KRb and KCs molecules (possessing a significant intrinsic electric dipole moment) spectroscopy, combined with theoretical results, the cooling of their internal degrees of freedom using Stimulated Raman Adiabatic Passage (STIRAP), a laser process bringing molecules towards their absolute ground state, has been modelled. Several STIRAP schemes have been investigated and compared regarding their efficiency. The RbCa molecule has then been studied, which spectroscopy is still unknown. The ability of controlling the anisotropic interactions induced by the simultaneous presence of an electric and magnetic dipole moment provided by this species is a clear advantage. The electronic structure of RbCa has been computed with two methods, thus allowing to estimate the reliability of the results. A scheme of laser transitions bringing to the formation of cold RbCa molecules from separate atoms has been proposed.Manipulating and trapping molecules relies on the precise knowledge of their response to an external electromagnetic field, characterised by their dynamic dipolar polarisability. The quantum chemistry calculations mentioned earlier allowed us to compute high-lying excited states, dynamic polarisability has then been computed for a whole set of diatomic molecules (alkali dimers, RbCa, RbSr, …). The optimal parameters for trapping those molecules has then been determined
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Abraham, Eric Roy I. "Photoassociative spectroscopy of collisions between ultracold lithium atoms." Thesis, 1996. http://hdl.handle.net/1911/16990.

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The spectra of the high-lying vibrational levels of the $A\sp1\Sigma\sbsp{u}{+}$ and $1\sp3\Sigma\sbsp{g}{+}$ singly excited states of both $\sp6\rm Li\sb2$ and $\sp7\rm Li\sb2$ are obtained via photoassociation of colliding ultracold atoms confined in a magneto-optical trap. The least bound state of the $a\sp3\Sigma\sbsp{u}{+}$ ground state potential, obtained by two-photon photoassociative spectroscopy, is also presented for both $\sp7\rm Li\sb2$ and $\sp6\rm Li\sb2$. The vibrational levels have resolved hyperfine structure, whose relative energy splittings and transition strengths are accurately modeled. The photoassociative spectra are used to precisely determine both the singlet and triplet s-wave scattering lengths for both isotopes, which are important parameters in systems designed to observe quantum degenerate effects and Bose-Einstein condensation.
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Ospelkaus, Christian [Verfasser]. "Fermi-Bose mixtures : from mean field interactions to ultracold chemistry / vorgelegt von Christian Ospelkaus." 2007. http://d-nb.info/983442231/34.

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Books on the topic "Ultracold chemistry"

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Pérez Ríos, Jesús. An Introduction to Cold and Ultracold Chemistry. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-55936-6.

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Mendoza, Rose Marie O. Introduction to Cold and Ultracold Chemistry. Arcler Education Inc, 2021.

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Krems, Roman V. Molecules in Electromagnetic Fields: From Ultracold Physics to Controlled Chemistry. Wiley & Sons, Limited, John, 2018.

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Krems, Roman V. Molecules in Electromagnetic Fields: From Ultracold Physics to Controlled Chemistry. Wiley & Sons, Limited, John, 2018.

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Krems, Roman V. Molecules in Electromagnetic Fields: From Ultracold Physics to Controlled Chemistry. Wiley & Sons, Incorporated, John, 2018.

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Krems, Roman V. Molecules in Electromagnetic Fields: From Ultracold Physics to Controlled Chemistry. Wiley & Sons, Incorporated, John, 2018.

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Ríos, Jesús Pérez. Introduction to Cold and Ultracold Chemistry: Atoms, Molecules, Ions and Rydbergs. Springer International Publishing AG, 2020.

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Ríos, Jesús Pérez. Introduction to Cold and Ultracold Chemistry: Atoms, Molecules, Ions and Rydbergs. Springer International Publishing AG, 2021.

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Book chapters on the topic "Ultracold chemistry"

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McDonald, Mickey. "Photodissociation and Ultracold Chemistry." In High Precision Optical Spectroscopy and Quantum State Selected Photodissociation of Ultracold 88Sr2 Molecules in an Optical Lattice, 161–82. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-68735-3_8.

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Pérez Ríos, Jesús. "Ultracold Gases." In An Introduction to Cold and Ultracold Chemistry, 37–53. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-55936-6_3.

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Pérez Ríos, Jesús. "Ultracold Molecular Collisions." In An Introduction to Cold and Ultracold Chemistry, 83–118. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-55936-6_5.

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Pérez Ríos, Jesús. "Rydberg-Neutral Ultracold Chemical Reactions." In An Introduction to Cold and Ultracold Chemistry, 155–70. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-55936-6_8.

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Quéméner, Goulven. "CHAPTER 12. Ultracold Collisions of Molecules." In Theoretical and Computational Chemistry Series, 579–632. Cambridge: Royal Society of Chemistry, 2017. http://dx.doi.org/10.1039/9781782626800-00579.

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Pérez Ríos, Jesús. "The Realm of Cold and Ultracold." In An Introduction to Cold and Ultracold Chemistry, 1–7. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-55936-6_1.

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Côté, Robin. "CHAPTER 7. Role of Resonances at Ultracold Temperatures." In Theoretical and Computational Chemistry Series, 313–88. Cambridge: Royal Society of Chemistry, 2017. http://dx.doi.org/10.1039/9781782626800-00313.

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Pérez Ríos, Jesús. "Ultracold Physics and the Quest of New Physics." In An Introduction to Cold and Ultracold Chemistry, 235–46. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-55936-6_12.

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Pérez Ríos, Jesús. "Ultracold Rydberg Atoms and Ultralong-Range Rydberg Molecules." In An Introduction to Cold and Ultracold Chemistry, 137–53. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-55936-6_7.

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Pérez Ríos, Jesús. "Few-Body Processes Involving Ions and Neutrals at Cold Temperatures." In An Introduction to Cold and Ultracold Chemistry, 193–214. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-55936-6_10.

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Conference papers on the topic "Ultracold chemistry"

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Bohn, John L. "Manipulation of Ultracold Chemistry." In Laser Science. Washington, D.C.: OSA, 2010. http://dx.doi.org/10.1364/ls.2010.lthb1.

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Kupper, J., H. L. Bethlem, F. M. H. Crompvoets, S. Y. T. van de Meerakker, N. Vanhaecke, J. van Veldhoven, K. Wohlfart, and G. Meijer. "Towards ultracold chemistry; manipulation of polar molecules with electric fields." In International Quantum Electronics Conference, 2005. IEEE, 2005. http://dx.doi.org/10.1109/iqec.2005.1560872.

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Ospelkaus, Silke, Amodsen Chotia, Marcio de Miranda, Brian Neyenhuis, Kang-Kuen Ni, Dajun Wang, Jun Ye, and Deborah Jin. "Ultracold chemistry and dipolar collisions in a quantum gas of polar molecules." In 12th European Quantum Electronics Conference CLEO EUROPE/EQEC. IEEE, 2011. http://dx.doi.org/10.1109/cleoe.2011.5942919.

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Ni, Kang-Kuen. "CHEMISTRY IN THE ULTRACOLD REGIME: PRECISION MOLECULAR ASSEMBLY AND TEST OF STATISTICAL REACTION DYNAMICS." In 2022 International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2022. http://dx.doi.org/10.15278/isms.2022.ma02.

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Reports on the topic "Ultracold chemistry"

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Dudley R. Herschbach. Chemistrty with Ultracold Molecules. Office of Scientific and Technical Information (OSTI), December 2008. http://dx.doi.org/10.2172/942272.

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Journal articles
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