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Institution

Paul Scherrer Institute

FacilityVilligen, Switzerland
About: Paul Scherrer Institute is a facility organization based out in Villigen, Switzerland. It is known for research contribution in the topics: Neutron & Large Hadron Collider. The organization has 9248 authors who have published 23984 publications receiving 890129 citations. The organization is also known as: PSI.


Papers
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Journal ArticleDOI
TL;DR: In this article, the Weyl semimetal state in an inversion-symmetry-breaking single-crystalline solid, Niobium arsenide (NbAs), has been discovered.
Abstract: Three types of fermions play a fundamental role in our understanding of nature: Dirac, Majorana and Weyl. Whereas Dirac fermions have been known for decades, the latter two have not been observed as any fundamental particle in high-energy physics, and have emerged as a much-sought-out treasure in condensed matter physics. A Weyl semimetal is a novel crystal whose low-energy electronic excitations behave as Weyl fermions. It has received worldwide interest and is believed to open the next era of condensed matter physics after graphene and three-dimensional topological insulators. However, experimental research has been held back because Weyl semimetals are extremely rare in nature. Here, we present the experimental discovery of the Weyl semimetal state in an inversion-symmetry-breaking single-crystalline solid, niobium arsenide (NbAs). Utilizing the combination of soft X-ray and ultraviolet photoemission spectroscopy, we systematically study both the surface and bulk electronic structure of NbAs. We experimentally observe both the Weyl cones in the bulk and the Fermi arcs on the surface of this system. Our ARPES data, in agreement with our theoretical band structure calculations, identify the Weyl semimetal state in NbAs, which provides a real platform to test the potential of Weyltronics. Experiments show that niobium arsenide is a Weyl semimetal.

754 citations

Journal ArticleDOI
S. Chatrchyan, Vardan Khachatryan, Albert M. Sirunyan, A. Tumasyan  +2268 moreInstitutions (158)
TL;DR: In this article, the transverse momentum balance in dijet and γ/Z+jets events is used to measure the jet energy response in the CMS detector, as well as the transversal momentum resolution.
Abstract: Measurements of the jet energy calibration and transverse momentum resolution in CMS are presented, performed with a data sample collected in proton-proton collisions at a centre-of-mass energy of 7TeV, corresponding to an integrated luminosity of 36pb−1. The transverse momentum balance in dijet and γ/Z+jets events is used to measure the jet energy response in the CMS detector, as well as the transverse momentum resolution. The results are presented for three different methods to reconstruct jets: a calorimeter-based approach, the ``Jet-Plus-Track'' approach, which improves the measurement of calorimeter jets by exploiting the associated tracks, and the ``Particle Flow'' approach, which attempts to reconstruct individually each particle in the event, prior to the jet clustering, based on information from all relevant subdetectors

750 citations

Journal ArticleDOI
01 May 2005-Carbon
TL;DR: In this paper, the authors suggest that the limitation of C g can be attributed to a space constriction for charge accommodation inside the pore walls, and that the use of extremely high surface area carbons for EDLCs may be unprofitable.

739 citations

Journal ArticleDOI
Joao Almeida1, Joao Almeida2, Siegfried Schobesberger3, Andreas Kürten2, Ismael K. Ortega3, Oona Kupiainen-Määttä3, Arnaud P. Praplan4, Alexey Adamov3, António Amorim5, F. Bianchi4, Martin Breitenlechner6, A. David1, Josef Dommen4, Neil M. Donahue7, Andrew J. Downard8, Eimear M. Dunne9, Jonathan Duplissy3, Sebastian Ehrhart2, Richard C. Flagan8, Alessandro Franchin3, Roberto Guida1, Jani Hakala3, Armin Hansel6, Martin Heinritzi6, Henning Henschel3, Tuija Jokinen3, Heikki Junninen3, Maija Kajos3, Juha Kangasluoma3, Helmi Keskinen10, Agnieszka Kupc11, Theo Kurtén3, Alexander N. Kvashin12, Ari Laaksonen13, Ari Laaksonen10, Katrianne Lehtipalo3, Markus Leiminger2, Johannes Leppä13, Ville Loukonen3, Vladimir Makhmutov12, Serge Mathot1, Matthew J. McGrath14, Tuomo Nieminen3, Tuomo Nieminen15, Tinja Olenius3, Antti Onnela1, Tuukka Petäjä3, Francesco Riccobono4, Ilona Riipinen16, Matti P. Rissanen3, Linda Rondo2, Taina Ruuskanen3, Filipe Duarte Santos5, Nina Sarnela3, Simon Schallhart3, R. Schnitzhofer6, John H. Seinfeld8, Mario Simon2, Mikko Sipilä15, Mikko Sipilä3, Yuri Stozhkov12, Frank Stratmann17, António Tomé5, Jasmin Tröstl4, Georgios Tsagkogeorgas17, Petri Vaattovaara10, Yrjö Viisanen13, Annele Virtanen10, Aron Vrtala11, Paul E. Wagner11, Ernest Weingartner4, Heike Wex17, Christina Williamson2, Daniela Wimmer3, Daniela Wimmer2, Penglin Ye7, Taina Yli-Juuti3, Kenneth S. Carslaw9, Markku Kulmala3, Markku Kulmala15, Joachim Curtius2, Urs Baltensperger4, Douglas R. Worsnop, Hanna Vehkamäki3, Jasper Kirkby1, Jasper Kirkby2 
17 Oct 2013-Nature
TL;DR: The results show that, in regions of the atmosphere near amine sources, both amines and sulphur dioxide should be considered when assessing the impact of anthropogenic activities on particle formation.
Abstract: Nucleation of aerosol particles from trace atmospheric vapours is thought to provide up to half of global cloud condensation nuclei(1). Aerosols can cause a net cooling of climate by scattering sun ...

738 citations

Journal ArticleDOI
19 Nov 2015-Nature
TL;DR: Flexible compounds Fe(bdp) and Co(BDp) (bdp2− = 1,4-benzenedipyrazolate) are shown to undergo a structural phase transition in response to specific CH4 pressures, resulting in adsorption and desorption isotherms that feature a sharp ‘step’.
Abstract: Two flexible metal-organic frameworks are presented as solid adsorbents for methane that undergo reversible phase transitions at specific methane pressures, enabling greater storage capacities of usable methane than have been achieved previously, while also providing internal heat management of the system. Natural gas — methane — is a clean and cheap fuel but its usefulness in transport applications is limited by storage problems, given its low energy density per unit volume under ambient conditions compared with petrol or diesel. One way of increasing methane storage capacity is to use tanks containing porous materials, such as metal–organic frameworks, as a storage medium. However, for every methane molecule adsorbed and desorbed there is an associated thermal fluctuation that could cause overheating or reduce storage efficiency if left unchecked. Here Jeffrey Long and colleagues describe two flexible metal–organic frameworks that undergo reversible phase transitions at specific methane pressures, enabling greater storage capacities of usable methane than have been achieved previously, while also providing internal heat management of the system. As a cleaner, cheaper, and more globally evenly distributed fuel, natural gas has considerable environmental, economic, and political advantages over petroleum as a source of energy for the transportation sector1,2. Despite these benefits, its low volumetric energy density at ambient temperature and pressure presents substantial challenges, particularly for light-duty vehicles with little space available for on-board fuel storage3. Adsorbed natural gas systems have the potential to store high densities of methane (CH4, the principal component of natural gas) within a porous material at ambient temperature and moderate pressures4. Although activated carbons, zeolites, and metal–organic frameworks have been investigated extensively for CH4 storage5,6,7,8, there are practical challenges involved in designing systems with high capacities and in managing the thermal fluctuations associated with adsorbing and desorbing gas from the adsorbent. Here, we use a reversible phase transition in a metal–organic framework to maximize the deliverable capacity of CH4 while also providing internal heat management during adsorption and desorption. In particular, the flexible compounds Fe(bdp) and Co(bdp) (bdp2− = 1,4-benzenedipyrazolate) are shown to undergo a structural phase transition in response to specific CH4 pressures, resulting in adsorption and desorption isotherms that feature a sharp ‘step’. Such behaviour enables greater storage capacities than have been achieved for classical adsorbents9, while also reducing the amount of heat released during adsorption and the impact of cooling during desorption. The pressure and energy associated with the phase transition can be tuned either chemically or by application of mechanical pressure.

737 citations


Authors

Showing all 9348 results

NameH-indexPapersCitations
Andrea Bocci1722402176461
Tobin J. Marks1591621111604
Wolfgang Wagner1562342123391
David D'Enterria1501592116210
Andreas Pfeiffer1491756131080
Christoph Grab1441359144174
Maurizio Pierini1431782104406
Alexander Belyaev1421895100796
Ajit Kumar Mohanty141112493062
Felicitas Pauss1411623104493
Chiara Mariotti141142698157
Luc Pape1411441130253
Rainer Wallny1411661105387
Roland Horisberger1391471100458
Emmanuelle Perez138155099016
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
202363
2022199
20211,299
20201,442
20191,330
20181,298