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BEGIN:VEVENT
SUMMARY:A Morphotropic Phase Boundary in Samarium-modified Bismuth Ferrite
  Thin Films
DTSTART;VALUE=DATE-TIME:20160204T214500Z
DTEND;VALUE=DATE-TIME:20160204T221500Z
DTSTAMP;VALUE=DATE-TIME:20260809T080213Z
UID:indico-contribution-153-530@events01.synchrotron.org.au
DESCRIPTION:Speakers: Nagarajan Valanoor (UNSW Australia)\nInterfacial con
 trol of a polar (rhombohedral)-to-non-polar (orthorhombic) phase transitio
 n in (001) oriented epitaxial BiFeO3/(Bi1-xSmx)FeO3 superlattices is prese
 nted. We demonstrate controlling the composition at which a polar phase tr
 ansformation takes place by tuning the strength of the interlayer interact
 ions while holding the average composition constant.  It is shown that the
  thickness of the superlattice layers have a strong influence on the inter
 layer polar coupling\, which in turn changes the phase transition. For sho
 rtest periods studied (layers 5 and 10 nm thick) the onset of the phase tr
 ansition is suppressed along with a significant broadening (as a function 
 of Sm3+ concentration) of an incommensurately modulated phase\, determined
  by two-dimensional x-ray diffraction mapping. Consequently\, ferroelectri
 c character with robust polarization hysteresis and enhanced dielectric co
 nstant\, is observed even for substitution concentration of Sm3+ which wou
 ld otherwise lead to a leaky paraelectric in single-layer (Bi1-xSmx)FeO3 f
 ilms. The experimental results are fully consistent with a mean-field ther
 modynamic theory which reveals that the strength of the interlayer couplin
 g is strongly affected by the polar-polar interaction across the interface
 . Part of this work appears in Phys. Rev. B 90\, 245131(2014).\n\nhttps://
 events01.synchrotron.org.au/event/19/contributions/530/
LOCATION:
URL:https://events01.synchrotron.org.au/event/19/contributions/530/
END:VEVENT
BEGIN:VEVENT
SUMMARY:Crystalline self-stratification in polymer thin films
DTSTART;VALUE=DATE-TIME:20160202T230000Z
DTEND;VALUE=DATE-TIME:20160202T233000Z
DTSTAMP;VALUE=DATE-TIME:20260809T080213Z
UID:indico-contribution-153-526@events01.synchrotron.org.au
DESCRIPTION:Speakers: Eliot Gann (Australian Synchrotron)\nThe orientation
  of molecules within thin films is of critical importance to the emerging 
 field of organic electronics.  Particularly in the case of solution proces
 sable polymers and small molecules\, where alkyl side chains\, included fo
 r solubility\, impede conduction along that molecular direction\, understa
 nding and controlling the molecular orientation both at surfaces and in th
 e bulk of thin films is increasingly important to further increase electro
 nic performance.  Grazing Incidence Wide Angle X-ray Scattering has been w
 idely used to look at the orientation of crystallites within films\, but a
  capability which has not been widely used is its potential to characteriz
 e the depth within films at which different kinds of molecular stacking oc
 cur.  Using very fine control over the angle of incidence of the X-ray bea
 m\, we observe a distinct segregation of edge-on crystallinity in a film o
 f the polymer PNDI-SVS which otherwise stacks in a highly face-on orientat
 ion.  Using simulations of the X-ray Electric Field Intensity within the f
 ilm\, the angular variation of scattering intensity can be matched\, resul
 ting in the conclusion that the surface region extends 9 nm into the 72 nm
  film.  \n\nDuring the spin-coating deposition process\, a face-on orienta
 tion is initially observed\, likely the result of preaggregation in soluti
 on in combination with a relatively fast-drying solvent. The stratified mo
 rphology is produced by annealing the film for a brief time\, while upon f
 urther annealing\, the bulk of the film eventually reorients to become edg
 e-on\, suggesting that the stratification is a non-equilibrium\, kinetical
 ly-trapped state. With brief annealing\, only the surface region of the fi
 lm has time to reorient to the ultimately lower energy edge-on orientation
 .  The time and temperature of this reorganization can reveal the differen
 ce in energetics at different depths within the film\, illustrating how gr
 azing incidence scattering can open up the possibility of examining thin f
 ilms in novel and important ways.\n\nhttps://events01.synchrotron.org.au/e
 vent/19/contributions/526/
LOCATION:
URL:https://events01.synchrotron.org.au/event/19/contributions/526/
END:VEVENT
BEGIN:VEVENT
SUMMARY:The endless possibilities of graphene on heteroepitaxial silicon c
 arbide
DTSTART;VALUE=DATE-TIME:20160203T214500Z
DTEND;VALUE=DATE-TIME:20160203T221500Z
DTSTAMP;VALUE=DATE-TIME:20260809T080213Z
UID:indico-contribution-153-521@events01.synchrotron.org.au
DESCRIPTION:Speakers: Francesca Iacopi (Griffith University\, Queensland M
 icro and Nanotechnology Centre)\nEpitaxial graphene grown using solid sour
 ce carbon from silicon carbide wafers has been for long time the only rout
 e to obtain high quality graphene directly grown at the wafer –level\, w
 hich is crucial to realise the promise of graphene for nanodevices. Noneth
 eless\, the capability of obtaining comparable quality of graphene on sili
 con as opposed to silicon carbide wafers\, would open an immense opportuni
 ty for graphene in integrated circuits and micro-systems in general. While
  encouraging results have been obtained through thermal decomposition of h
 eteroepitaxial SiC films on silicon wafers\, this has usually been limited
  to small areas and to the use of Si (111) surfaces. Moreover\, the obtain
 ed graphene quality tends to be strongly hampered by the upper limitation 
 in synthesis temperature set by the melting temperature of silicon.  \nWe 
 have recently demonstrated for the first time that most of those limitatio
 ns can be overcome with the use of heteroepitaxial silicon carbide films i
 n combination with a catalytic alloy of nickel and copper. With this appro
 ach we obtain 2 layers graphene on silicon carbide with uniform coverage o
 ver the silicon wafer and an average ID/IG ratio of about 0.2 +/- 0.05 [1]
 \, indicating a substantial improvement as compared to a ratio of ~1 and a
 bove of graphene through the more conventional thermal decomposition. This
  novel catalytic approach on silicon holds high promise for integrated app
 lications also through the capability for straightforward graphene micropa
 tterning through self-aligned synthesis on pre-structured silicon carbide 
 on silicon [2]. Moreover\, we have demonstrated the potential for this app
 roach to fabricate high –performing electrodes for integrated supercapac
 itor structures [3].\n[1] F.Iacopi\, N.Mishra\, B.V.Cunning\, D.Goding\, S
 .Dimitrijev\, R.Brock\, R.H.Dauskardt\, B.Wood and J.J.Boeckl\, “A catal
 ytic alloy approach for highly uniform graphene on epitaxial SiC on silico
 n wafers”\, J.Mater.Res.30(5)\, 609-616\, 2015.\n[2] B.V.Cunning\, M.Ahm
 ed\, N.Mishra\, A.R.Kermany\, B.Wood\, F.Iacopi\, “Graphitized silicon c
 arbide microbeams on silicon: wafer-level\, self -aligned graphene on sili
 con wafers”\, Nanotechnology 25\, 325301\, 2014.\n[3] M.Ahmed\, M.Khawaj
 a\, M.Notarianni\, B.Wang\, D.Goding\, B.Gupta\, J.J. Boeckl\, A.Takshi\, 
 N.Motta\, S.E.Saddow\, F.Iacopi\, “A thin film approach for SiC–derive
 d graphene as an on-chip electrode for supercapacitors”\, Nanotechnology
  26\, 434005\, 2015.\n\nhttps://events01.synchrotron.org.au/event/19/contr
 ibutions/521/
LOCATION:
URL:https://events01.synchrotron.org.au/event/19/contributions/521/
END:VEVENT
BEGIN:VEVENT
SUMMARY:Pluto: the next frontier for studies of condensed matter
DTSTART;VALUE=DATE-TIME:20160202T220000Z
DTEND;VALUE=DATE-TIME:20160202T223000Z
DTSTAMP;VALUE=DATE-TIME:20260809T080213Z
UID:indico-contribution-153-520@events01.synchrotron.org.au
DESCRIPTION:Speakers: Helen Brand (Australian Synchrotron.)\nIn July this 
 year\, the NASA New Horizons spacecraft completed an historic flyby of the
  Plutonian system\, the first spacecraft to visit Pluto. The long-awaited 
 data from this mission will take months to be returned in full to Earth. H
 owever\, the wealth of data received so far\, although small in volume\, i
 s already providing amazing insights into the surface morphology and geoch
 emistry of Pluto and providing important clues into the inner workings of 
 this dwarf planet.\n\nNew Horizons is equipped with high resolution imagin
 g cameras as well as geochemical equipment to investigate surface and atmo
 spheric compositions. Using a combination of geological mapping\, geochemi
 cal data and other physical measurements\, planetary scientists aim to det
 ermine the processes that shape the interior and surface of Pluto and othe
 r outer solar system objects. \n\nIn situ studies of the materials found o
 n bodies within the outer solar system is an emerging area\, both for plan
 etary science and for research in Australia. The conditions of the icy sat
 ellites are simulated while data\, typically diffraction\, (X-ray or neutr
 on)\, or IR data\, is recorded. The observations and material properties o
 btained in these studies can then be used as a comparison to spacecraft da
 ta or an input to models of geological processes. \n\nThis contribution wi
 ll include a background introduction to the New Horizons mission\, an over
 view of the findings and data so far\, and a discussion of how structural 
 condensed matter studies\, particularly synchrotron and neutron studies\, 
 can unlock the processes that govern the outer solar system.\n\nhttps://ev
 ents01.synchrotron.org.au/event/19/contributions/520/
LOCATION:
URL:https://events01.synchrotron.org.au/event/19/contributions/520/
END:VEVENT
BEGIN:VEVENT
SUMMARY:Towards Realisation of High-Performance Thermoelectrics for Energy
  Conversion
DTSTART;VALUE=DATE-TIME:20160203T040000Z
DTEND;VALUE=DATE-TIME:20160203T043000Z
DTSTAMP;VALUE=DATE-TIME:20260809T080213Z
UID:indico-contribution-153-507@events01.synchrotron.org.au
DESCRIPTION:Speakers: Zhigang Chen (the University of Queensland)\nThermoe
 lectric materials directly convert thermal energy into electrical energy\,
  offering a green and sustainable alternative for the global energy market
 .[1\, 2] So far\, extensive investigations have been made to improve the t
 hermoelectric efficiency\, which governed by the dimensionless figure-of-m
 erit ZT ( )\, where σ is the electrical conductivity\, S is the Seebeck c
 oefficient\, T is the absolute temperature\, and  is the total thermal 
 conductivity which is the sum of the contributions from its electron (e
 ) and lattice (L) components. Here\, we developed cost-effective\, and 
 low-toxic thermoelectrics for high-efficiency energy conversion using nove
 l industry-level approach\, coupled with nanostructure and band engineerin
 g strategies. Through effective design of thermoelectric materials with en
 gineered chemistry and unique structure\, and advanced manufacturing\, hig
 h-performance thermoelectrics\, such as Cu2Se\,[3] Bi2Se3\,[4] Bi2Te3\,[5-
 8] In3Se4\,[9\, 10] etc.\, have been realised in our group. Such innovativ
 e technology can be used for harvesting electricity from waste heat or sun
  light. \n\nReferences\n[1]    Z.-G. Chen\, G. Han\, L. Yang\, et al.\, Pr
 og. Nat. Sci. 2012\, 22\, 535.\n[2]    G. Han\, Z.-G. Chen\, J. Drennan\, 
 et al.\, Small 2014\, 10\, 2747.\n[3]    L. Yang\, Z.-G. Chen\, G. Han\, e
 t al.\, Nano Energy 2015\, 16\, 367.\n[4]    M. Hong\, Z.-G. Chen\, L. Yan
 g\, et al.\, Adv. Elect. Mater. 2015\, 1\, 201500025.\n[5]    G. Han\, Z.-
 G. Chen\, L. Yang\, et al.\, Acs Appl. Mater. Inter. 2015\, 7\, 989.\n[6] 
    L. Cheng\, Z.-G. Chen\, L. Yang\, et al.\, J. Phy. Chem. C 2013\, 117\,
  12458.\n[7]    L. Yang\, Z.-G. Chen\, M. Hong\, et al.\, ACS Appl. Mater.
  Inter. 2015\, 7\, 23694.\n[8]    L. Cheng\, Z.-G. Chen\, S. Ma\, et al.\,
  J. Am. Chem. Soc. 2012\, 134\, 18920.\n[9]    G. Han\, Z.-G. Chen\, L. Ya
 ng\, et al.\, Cryst. Growth & Design 2013\, 13\, 5092.\n[10]    G. Han\, Z
 .-G. Chen\, C. Sun\, et al.\, CrystEngComm 2014\, 16\, 393.\n\nhttps://eve
 nts01.synchrotron.org.au/event/19/contributions/507/
LOCATION:
URL:https://events01.synchrotron.org.au/event/19/contributions/507/
END:VEVENT
BEGIN:VEVENT
SUMMARY:Atomic-scale understanding of CO2 adsorption processes in metal-or
 ganic framework (MOF) materials using neutron scattering and ab initio cal
 culations
DTSTART;VALUE=DATE-TIME:20160204T000000Z
DTEND;VALUE=DATE-TIME:20160204T003000Z
DTSTAMP;VALUE=DATE-TIME:20260809T080213Z
UID:indico-contribution-153-497@events01.synchrotron.org.au
DESCRIPTION:Speakers: Josie Auckett (ANSTO)\nThe dependence of the industr
 ialised world on fossil-fuel energy generation technologies and consequent
  increase in atmospheric CO2 concentrations has been blamed for emerging a
 dverse climate effects\, including an increase in global mean temperatures
  [1]. Until renewable\, carbon-free energy sources can be efficiently harn
 essed to meet the world’s energy needs\, interim measures are sought to 
 suppress the atmospheric release of CO2 from traditional coal and natural 
 gas combustion processes. Microporous materials such as zeolites and metal
 -organic frameworks (MOFs) are therefore being investigated for the separa
 tion and capture of CO2 at various stages of the combustion cycle. \n\nMOF
 s represent one of the most promising classes of materials for this applic
 ation\, offering unrivalled tunability of structural and chemical characte
 ristics via the substitution of metals and choice and functionalisation of
  ligands [2]. In order for a MOF to be rationally tuned for improved perfo
 rmance\, the nature of the interactions between the host framework and gue
 st molecules must be well-understood at the atomic level. Our research tar
 gets this detailed understanding of MOFs using neutron scattering and comp
 utational methods. \n\nWe are currently investigating several MOFs which d
 isplay unexpected sorption properties such as “reverse sieving” – th
 at is\, selectively absorbing larger gas molecules while rejecting smaller
  ones – and unusual lattice expansion effects. Using in situ diffraction
  to locate the preferred binding sites of guest molecules in the framework
 \, inelastic neutron scattering to probe system dynamics\, and density fun
 ctional theory-based molecular dynamics simulations to validate and interp
 ret our experimental results\, we are able to gain detailed information ab
 out the mechanisms of gas uptake and diffusion in these exciting new MOF m
 aterials.\n\n[1] S. Solomon\, G.K. Plattner et al.\, Proc. Natl. Acad. Sci
 . USA **106** (2009) 1704-1709.\n\n[2] G.J. Kearley & V.K. Peterson (eds.)
 \, Neutron Applications in Materials\, Springer (2015).\n\nhttps://events0
 1.synchrotron.org.au/event/19/contributions/497/
LOCATION:
URL:https://events01.synchrotron.org.au/event/19/contributions/497/
END:VEVENT
BEGIN:VEVENT
SUMMARY:X-radiation in health and disease: Novel approaches to the study o
 f disease processes and therapy
DTSTART;VALUE=DATE-TIME:20160204T030000Z
DTEND;VALUE=DATE-TIME:20160204T033000Z
DTSTAMP;VALUE=DATE-TIME:20260809T080213Z
UID:indico-contribution-153-476@events01.synchrotron.org.au
DESCRIPTION:Speakers: Damian Myers (The University of Melbourne)\nOur curr
 ent medical knowledge and understanding of human biology and physiology ha
 ve been predicated by our capacity to image organs\, body structures\, dif
 ferent types of tissues and particular cell types. These imaging modalitie
 s range from advanced microscopy for imaging of cells and tissues through 
 to 2D and 3D macroscopic techniques for imaging of tissues and organs. Sof
 t tissues in particular are difficult to image\, especially when surrounde
 d by dense structures such as bone. Also\, some regions\, such as the brai
 n\, require special investigative techniques as they are closed tissue/org
 an structures with low contrast features.\n\nMedical diagnoses\, monitorin
 g of disease progression\, efficacy of therapies and the recent advent of 
 ‘targeted imaging’ rely upon techniques such as X-ray analysis\, MRI\,
  Positron Emission Tomography (PET) and more.  In this seminar several rec
 ent adaptions of X-ray and synchrotron-based X-ray science will be related
 . In particular\, Phase-contrast X-ray imaging (PCXI)\, also termed microf
 ocus imaging\, X-ray Fluorescence Microscopy (XFM) and Microbeam X-ray The
 rapy (MRT) will be discussed. \n\nSince the discovery of X-rays and develo
 pment of medical X-ray sources\, X-ray imaging has accounted for approxima
 tely 60% of medical diagnostic procedures\; X-ray imaging is still the pre
 dominant technology used in medicine. Over the past 30 years radioisotope-
 based imaging has expanded substantially with 3D positron emission tomogra
 phy (PET) and combined PET/MRI being developed for simultaneous structural
  and functional imaging.  More recently\, advanced 3D imaging techniques h
 ave been aligned with targeted therapies and high resolution multi-modal i
 maging to improve our capabilities in definition of organ boundaries and p
 articular tumours and organ abnormalities. Microbeam radiation therapy (MR
 T) is another capability and this is currently being developed at the Aust
 ralian Synchrotron. \n\nSynchrotrons produce a broad range of electromagne
 tic radiation applicable for diverse analyses such protein crystallography
 \, X-radiation for fluorescence spectroscopy\, for mapping and quantificat
 ion of trace metals\, and for fast X-ray tomography for structural imaging
 . Access to synchrotron light sources has led to a renaissance in utilisat
 ion of X-rays for diverse imaging applications and novel radiation therapi
 es.  \n\nDuring this seminar the importance of advanced imaging techniques
  and synchrotron radiation to enable investigation of a range of diseases 
 will be related. This presentation will include specific studies in which 
 application of synchrotron radiation has aided investigations into bone di
 sease and bone cancers\, the study of brain abnormalities including epilep
 sy and traumatic brain injury and targeted therapy using MRT. \n\nAdvanced
  medical imaging techniques have been central to our understanding of dise
 ase processes and have the potential to aid clinicians when considering th
 erapeutic interventions. The strong synergy that occurs in interdisciplina
 ry research has been crucial to these developments. Project design and eff
 icient implementation of advanced imaging techniques to achieve meaningful
  outcomes in science and medicine will also be discussed.\n\nAcknowledgeme
 nt: The contribution of the many scientists and organisations involved wit
 h this work will be related during delivery of this invited seminar.\n\nht
 tps://events01.synchrotron.org.au/event/19/contributions/476/
LOCATION:
URL:https://events01.synchrotron.org.au/event/19/contributions/476/
END:VEVENT
BEGIN:VEVENT
SUMMARY:Two-dimensional Coulomb gas at negative temperature
DTSTART;VALUE=DATE-TIME:20160205T000000Z
DTEND;VALUE=DATE-TIME:20160205T003000Z
DTSTAMP;VALUE=DATE-TIME:20260809T080213Z
UID:indico-contribution-153-468@events01.synchrotron.org.au
DESCRIPTION:Speakers: Tapio Simula (Monash University)\nLars Onsager is pe
 rhaps best known as the recipient of 1968 Nobel Prize in chemistry and by 
 his tour de force solution to the two-dimensional Ising model. However\, h
 is remarkable insight predicting the quantisation of vorticity in superflu
 id helium and the statistical mechanics description of two-dimensional tur
 bulence have received much less attention. In this talk\, I will  briefly 
 review certain aspects of the problem of two-dimensional turbulence with a
  particular emphasis on Onsager’s statistical hydrodynamics model. I wil
 l then apply this model to turbulent superfluid Bose—Einstein condensate
 s in which the quantised vortices have a long-range effective interaction 
 and can be mapped to a two-dimensional Coulomb gas of positive and negativ
 e charged particles. By observing the dynamics of such vortex charges in n
 umerical simulations we have found them to spontaneously arrange to large 
 scale vortex clusters\, coined Onsager vortices\, that correspond to absol
 ute negative Boltzmann temperatures [1]. I will discuss the microscopic me
 chanism leading to the emergence of such novel states of matter. Finally\,
  I will outline the recent progress in Australia and elsewhere toward expe
 rimentally observing such states [2] with the prospect of realising Onsage
 r’s prediction of super vortices in two-dimensional fluid turbulence.  \
 n\n\n[1]  “Emergence of Order from Turbulence in an Isolated Planar Supe
 rfluid”\,\nTapio Simula\, Matthew J. Davis\, and Kristian Helmerson\,\nP
 hysical Review Letters **113**\, 165302 (2014).\n\n[2] “Vortex Gyroscope
  Imaging of Planar Superfluids”\, A. T. Powis\, S. J. Sammut\, and T
 . P. Simula\, Physical Review Letters **113**\, 165303 (2014).\n\nhttps:
 //events01.synchrotron.org.au/event/19/contributions/468/
LOCATION:
URL:https://events01.synchrotron.org.au/event/19/contributions/468/
END:VEVENT
BEGIN:VEVENT
SUMMARY:Engineering the Diamond Surface for Quantum Technologies
DTSTART;VALUE=DATE-TIME:20160203T030000Z
DTEND;VALUE=DATE-TIME:20160203T033000Z
DTSTAMP;VALUE=DATE-TIME:20260809T080213Z
UID:indico-contribution-153-455@events01.synchrotron.org.au
DESCRIPTION:Speakers: Alastair Stacey (Centre of Excellence for Quantum Co
 mputation and Communication Technology\, The University of Melbourne)\nQua
 ntum technologies promise exciting and transformative futures in many area
 s of human endeavour. An example is the field of bio-sensing\, where quant
 um probes are already being used to answer fundamental questions about liv
 ing cells. In these applications diamond often takes centre stage\, as a m
 aterial which simultaneously exhibits both bio-friendly and quantum-friend
 ly properties. This presentation will review efforts to exploit diamond fo
 r quantum bio-sensing applications\, encompassing practical cellular measu
 rements to the development of fundamentally new sensing techniques. In par
 ticular\, I will address the biggest materials challenge we currently face
 \, which is the presence of uncontrolled defects at the solid state surfac
 e\, and detail the use of surface science techniques\, based at the Austra
 lian Synchrotron\, to understand and re-engineer this important quantum/li
 fe interface.\n\nhttps://events01.synchrotron.org.au/event/19/contribution
 s/455/
LOCATION:
URL:https://events01.synchrotron.org.au/event/19/contributions/455/
END:VEVENT
BEGIN:VEVENT
SUMMARY:Quantitative Femtosecond Charge Transfer Dynamics at Organic/Elect
 rode Interfaces Studied by Core-Hole Clock Spectroscopy
DTSTART;VALUE=DATE-TIME:20160203T000000Z
DTEND;VALUE=DATE-TIME:20160203T003000Z
DTSTAMP;VALUE=DATE-TIME:20260809T080213Z
UID:indico-contribution-153-434@events01.synchrotron.org.au
DESCRIPTION:Speakers: Dongchen Qi (Department of Chemistry and Physics\, L
 IMS\, La Trobe University)\nOrganic semiconductors have important applicat
 ions in organic electronics and other novel hybrid devices. In these devic
 es\, the transport of charge carriers across the interfaces between organi
 c molecules and electrodes plays an important role in determining the devi
 ce performance. Charge transfer dynamics at these interfaces usually occur
 s at the several femtoseconds timescale which presents tremendous challeng
 es to conventional pumb-probe based time-resolved techniques. In this talk
 \, I will introduce our recent work in the application of synchrotron-base
 d core-hole clock (CHC) spectroscopy on the quantitative characterisation 
 of charge transfer dynamics in several model organic/electrode systems. Th
 e CHC technique allows us to quantify the interfacial charge transfer time
 s with element and site/orbital specificity. Combined with other soft x-ra
 y spectroscopies\, it enables us to identify a few critical factors affect
 ing the charge transfer dynamics at organic/electrode interfaces.\n\n\n\n\
 n**Reference**\n\nL. Cao\, X.-Y. Gao\, A. T. S. Wee\, and D.-C. Qi\, *Adv.
  Mater.* **26**\, 7880 (2014).\n\nhttps://events01.synchrotron.org.au/even
 t/19/contributions/434/
LOCATION:
URL:https://events01.synchrotron.org.au/event/19/contributions/434/
END:VEVENT
END:VCALENDAR
