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Featured researches published by Joseph Pacold.


Review of Scientific Instruments | 2012

A plastic miniature x-ray emission spectrometer based on the cylindrical von Hamos geometry

B. A. Mattern; Gerald T. Seidler; M. Haave; Joseph Pacold; R. A. Gordon; J. Planillo; J. Quintana; B. Rusthoven

We present a short working distance miniature x-ray emission spectrometer (miniXES) based on the cylindrical von Hamos geometry. We describe the general design principles for the spectrometer and detail a specific implementation that covers Kβ and valence level emission from Fe. Large spatial and angular access to the sample region provides compatibility with environmental chambers, microprobe, and pump/probe measurements. The primary spectrometer structure and optic is plastic, printed using a 3-dimensional rapid-prototype machine. The spectrometer is inexpensive to construct and is portable; it can be quickly set up at any focused beamline with a tunable narrow bandwidth monochromator. The sample clearance is over 27 mm, providing compatibility with a variety of environment chambers. An overview is also given of the calibration and data processing procedures, which are implemented by a multiplatform user-friendly software package. Finally, representative measurements are presented. Background levels are below the level of the Kβ(2, 5) valence emission, the weakest diagram line in the system, and photometric analysis of count rates finds that the instrument is performing at the theoretical limit.


Journal of the American Chemical Society | 2014

Direct Observation of 4f Intrashell Excitation in Luminescent Eu Complexes by Time-Resolved X-ray Absorption Near Edge Spectroscopy

Joseph Pacold; David S. Tatum; Gerald T. Seidler; Kenneth N. Raymond; Xiaoyi Zhang; Andrew B. Stickrath; Devon R. Mortensen

We report time-resolved X-ray absorption near edge structure (TR-XANES) measurements at the Eu L3 edge upon photoexcitation of several Eu(III)-based luminescent lanthanide complexes. We find an unambiguous signature of the 4f intrashell excitation that occurs upon energy transfer from the photoactive organic antennas to the lanthanide species. Phenomenologically, this observation provides the basis for direct investigation of a crucial step in the energy transfer pathways that lead to sensitized luminescence in lanthanide-based dyes. Interestingly, the details of the TR-XANES feature suggest that the degree of 4f-5d hybridization may itself vary depending on the excited state of the Eu(III) ion.


Journal of Synchrotron Radiation | 2012

A miniature X-ray emission spectrometer (miniXES) for high-pressure studies in a diamond anvil cell.

Joseph Pacold; Joseph A. Bradley; Brian A. Mattern; Magnus Lipp; Gerald T. Seidler; Paul Chow; Yuming Xiao; Eric Rod; B. Rusthoven; John P. Quintana

Core-shell X-ray emission spectroscopy (XES) is a valuable complement to X-ray absorption spectroscopy (XAS) techniques. However, XES in the hard X-ray regime is much less frequently employed than XAS, often as a consequence of the relative scarcity of XES instrumentation having energy resolutions comparable with the relevant core-hole lifetimes. To address this, a family of inexpensive and easily operated short-working-distance X-ray emission spectrometers has been developed. The use of computer-aided design and rapid prototype machining of plastics allows customization for various emission lines having energies from ∼3 keV to ∼10 keV. The specific instrument described here, based on a coarsely diced approximant of the Johansson optic, is intended to study volume collapse in Pr metal and compounds by observing the pressure dependence of the Pr Lα emission spectrum. The collection solid angle is ∼50 msr, roughly equivalent to that of six traditional spherically bent crystal analyzers. The miniature X-ray emission spectrometer (miniXES) methodology will help encourage the adoption and broad application of high-resolution XES capabilities at hard X-ray synchrotron facilities.


Review of Scientific Instruments | 2014

A Laboratory-based Hard X-ray Monochromator for High-Resolution X-ray Emission Spectroscopy and X-ray Absorption Near Edge Structure Measurements

Gerald T. Seidler; Devon R. Mortensen; Aj Remesnik; Joseph Pacold; Na Ball; N. Barry; M. Styczinski; Oliver R. Hoidn

We report the development of a laboratory-based Rowland-circle monochromator that incorporates a low power x-ray (bremsstrahlung) tube source, a spherically bent crystal analyzer, and an energy-resolving solid-state detector. This relatively inexpensive, introductory level instrument achieves 1-eV energy resolution for photon energies of ∼5 keV to ∼10 keV while also demonstrating a net efficiency previously seen only in laboratory monochromators having much coarser energy resolution. Despite the use of only a compact, air-cooled 10 W x-ray tube, we find count rates for nonresonant x-ray emission spectroscopy comparable to those achieved at monochromatized spectroscopy beamlines at synchrotron light sources. For x-ray absorption near edge structure, the monochromatized flux is small (due to the use of a low-powered x-ray generator) but still useful for routine transmission-mode studies of concentrated samples. These results indicate that upgrading to a standard commercial high-power line-focused x-ray tube or rotating anode x-ray generator would result in monochromatized fluxes of order 10(6)-10(7) photons/s with no loss in energy resolution. This work establishes core technical capabilities for a rejuvenation of laboratory-based hard x-ray spectroscopies that could have special relevance for contemporary research on catalytic or electrical energy storage systems using transition-metal, lanthanide, or noble-metal active species.


Acta Crystallographica Section A | 2014

A Rebirth of Laboratory XANES and XES

Gerald T. Seidler; Devon R. Mortensen; Joseph Pacold; Oliver R. Hoidn

We have recently launched a reinvestigation of laboratory-based measurement of x-ray absorption near edge structure (XANES) and high-resolution x-ray emission spectroscopy (XES). Driven by the roughly one-hundred-fold improvement in the efficiency of high resolution x-ray optics compared to the 1970s, we have demonstrated that surprisingly impressive performance is now possible with laboratory XES instruments and that quite useful performance is possible for laboratory XANES. For applications in the 5 keV10 keV energy range, i.e., appropriate for 3d transition metal K edges and lanthanide L edges, we find XES performance that is intermediate between what can be achieved at bending-magnet and insertion-device beamlines at third generation synchrotron light sources. In the same energy range, we find that high quality XANES measurements can be performed in transmission mode on concentrated samples with the present instrument and should be possible, in many cases, in fluorescence mode after a planned upgrade brings the monochromatic beam flux up to approximately 10M/sec.


Journal of Physical Chemistry Letters | 2012

Fast Detection Allows Analysis of the Electronic Structure of Metalloprotein by X-ray Emission Spectroscopy at Room Temperature

Kathy Davis; Brian A. Mattern; Joseph Pacold; Taisiya Zakharova; Dale Brewe; Irina Kosheleva; Robert Henning; Tim Graber; Steve M. Heald; Gerald T. Seidler; Yulia Pushkar


Physical Review B | 2012

4f electron delocalization and volume collapse in praseodymium metal

Joseph A. Bradley; K. T. Moore; Magnus Lipp; Brian A. Mattern; Joseph Pacold; Gerald T. Seidler; Paul Chow; Eric Rod; Yuming Xiao; William J. Evans; CIW


Physical Review B | 2012

Real-space Green;s function calculations of Compton profiles

Brian A. Mattern; Gerald T. Seidler; Joshua J. Kas; Joseph Pacold; J. J. Rehr


Bulletin of the American Physical Society | 2015

Cross-relaxation quenching of x-ray excited luminescence in Eu-activated phosphors

Joseph Pacold; Devon R. Mortensen; William Reichlin; Zou Finfrock; Anthony Diaz; Gerald T. Seidler


Bulletin of the American Physical Society | 2014

Observation of internal excitation transfer in luminescent lanthanide materials by time-resolved X-ray absorption spectroscopy

Joseph Pacold; David S. Tatum; Gerald T. Seidler; Kenneth N. Raymond

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Eric Rod

Carnegie Institution for Science

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Joseph A. Bradley

Lawrence Livermore National Laboratory

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Magnus Lipp

Lawrence Livermore National Laboratory

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Paul Chow

Carnegie Institution for Science

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Yuming Xiao

Carnegie Institution for Science

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