skip to main content
US FlagAn official website of the United States government
dot gov icon
Official websites use .gov
A .gov website belongs to an official government organization in the United States.
https lock icon
Secure .gov websites use HTTPS
A lock ( lock ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.


Title: Externally Heated Diamond ANvil Cell Experimentation (EH-DANCE) for studying materials and processes under extreme conditions
Externally heated diamond anvil cells provide a stable and uniform thermal environment, making them a versatile device to simultaneously generate high-pressure and high-temperature conditions in various fields of research, such as condensed matter physics, materials science, chemistry, and geosciences. The present study features the Externally Heated Diamond ANvil Cell Experimentation (EH-DANCE) system, a versatile configuration consisting of a diamond anvil cell with a customized microheater for stable resistive heating, bidirectional pressure control facilitated by compression and decompression membranes, and a water-cooled enclosure suitable for vacuum and controlled atmospheres. This integrated system excels with its precise control of both pressure and temperature for mineral and materials science research under extreme conditions. We showcase the capabilities of the system through its successful application in the investigation of the melting temperature and thermal equation of state of high-pressure ice-VII at temperatures up to 1400 K. The system was also used to measure the elastic properties of solid ice-VII and liquid H2O using Brillouin scattering and Raman spectra of carbonates using Raman spectroscopy, highlighting the potential of the EH-DANCE system in high-pressure research.  more » « less
Award ID(s):
2246686 1829273 2127807
PAR ID:
10498495
Author(s) / Creator(s):
; ; ; ; ; ; ; ; ;
Publisher / Repository:
AIP Publishing
Date Published:
Journal Name:
Review of Scientific Instruments
Volume:
94
Issue:
12
ISSN:
0034-6748
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. When diamond anvil cell (DAC) sample chambers are outfitted with both thermal insulation and electrodes, two cutting-edge experimental methods are enabled: Joule heating with spectroradiometric temperature measurement and electrical resistance measurements of samples heated to thousands of kelvin. The accuracy of temperature and resistance measurements, however, often suffers from poor control of the shape and location of the sample, electrodes, and thermal insulation. Here, we present a recipe for the reproducible and precise fabrication of DAC sample, electrodes, and thermal insulation using a three-layer microassembly. The microassembly contains two potassium chloride thermal insulation layers, four electrical leads, a sample, and a buttressing layer made of polycrystalline alumina. The sample, innermost electrodes, and buttress layer are fabricated by focused-ion-beam milling. Three iron samples are presented as proof of concept. Each is successfully compressed and pulsed Joule heated while maintaining a four-point probe configuration. The highest pressure-temperature condition achieved is ∼150 GPa and 4000 K. 
    more » « less
  2. null (Ed.)
    In this work, the formation of carbide with the concertation of carbon at 0.1 at.% in refractory high-entropy alloy (RHEA) Mo15Nb20Re15Ta30W20 was studied under both ambient and high-pressure high-temperature conditions. The x-ray diffraction of dilute carbon (C)-doped RHEA under ambient pressure showed that the phases and lattice constant of RHEA were not influenced by the addition of 0.1 at.% C. In contrast, C-doped RHEA showed unexpected phase formation and transformation under combined high-pressure and high-temperature conditions by resistively employing the heated diamond anvil cell (DAC) technique. The new FCC_L12 phase appeared at 6 GPa and 809 °C and preserved the ambient temperature and pressure. High-pressure and high-temperature promoted the formation of carbides Ta3C and Nb3C, which are stable and may further improve the mechanical performance of the dilute C-doped alloy Mo15Nb20Re15Ta30W20. 
    more » « less
  3. Abstract Synchrotron‐based high‐pressure/high‐temperature single‐crystal X‐ray diffraction experiments to ~24 GPa and 700 K were conducted on eclogitic garnets (low‐Fe: Prp28Alm38Grs33Sps1and high‐Fe: Prp14Alm62Grs19Adr3Sps2) and omphacites (low‐Fe: Quad57Jd42Ae1and high‐Fe: Quad53Jd27Ae20), using an externally heated diamond anvil cell. Fitting the pressure‐volume‐temperature data to a third‐order Birch‐Murnaghan equation of state yields the thermoelastic parameters including bulk modulus (KT0), its pressure derivative (K′T0), temperature derivative ((∂KT/∂T)P), and thermal expansion coefficient (αT). The densities of the high‐Fe and low‐Fe eclogites were then modeled along typical geotherms of the normal mantle and the subducted oceanic crust to the transition zone depth (550 km). The metastable low‐Fe eclogite could be a reason for the stagnant slabs within the upper range of the transition zone. Eclogite would be responsible for density anomalies within 100–200 km in the upper mantle of Asia. 
    more » « less
  4. Severe plastic deformations (SPD) under high pressure, mostly by high-pressure torsion, are employed for producing nanostructured materials and stable or metastable high-pressure phases. However, they were studied postmortem after pressure release. Here, we review recent in situ experimental and theoretical studies of coupled SPD, strain-induced phase transformations (PTs), and microstructure evolution under high pressure obtained under compression in diamond anvil cell or compression and torsion in rotational diamond anvil cell. The utilization of x-ray diffraction with synchrotron radiation allows one to determine the radial distribution of volume fraction of phases, pressure, dislocation density, and crystallite size in each phase and the main laws of their evolution and interaction. Coupling with the finite element simulations of the sample behavior allows the determination of fields of all components of the stress and plastic strain tensors and volume fraction of high-pressure phase and provides a better understanding of ways to control occurring processes. Atomistic, nanoscale and scale-free phase-field simulations allow elucidation of the main physical mechanisms of the plastic strain-induced drastic reduction in phase transformation pressure (by one to two orders of magnitude), the appearance of new phases, and strain-controlled PT kinetics in comparison with hydrostatic loading. Combining in situ experiments with multiscale theory potentially leads to the formulation of methods to control strain-induced PT and microstructure evolution and designing economic synthetic paths for the defect-induced synthesis of desired high-pressure phases, nanostructures, and nanocomposites. 
    more » « less
  5. Abstract In this study, we conduct extensive high‐pressure experiments to investigate phase stability in the cobalt‐nitrogen system. Through a combination of synthesis in a laser‐heated diamond anvil cell, first‐principles calculations, Raman spectroscopy, and single‐crystal X‐ray diffraction, we establish the stability fields of known high‐pressure phases, hexagonal NiAs‐type CoN, and marcasite‐type CoN2within the pressure range of 50–90 GPa. We synthesize and characterize previously unknown nitrides, Co3N2,Pnma‐CoN and two polynitrides, CoN3and CoN5, within the pressure range of 90–120 GPa. Both polynitrides exhibit novel types of polymeric nitrogen chains and networks. CoN3feature branched‐type nitrogen trimers (N3) and CoN5show π‐bonded nitrogen chain. As the nitrogen content in the cobalt nitride increases, the CoN6polyhedral frameworks transit from face‐sharing (in CoN) to edge‐sharing (in CoN2and CoN3), and finally to isolated (in CoN5). Our study provides insights into the intricate interplay between structure evolution, bonding arrangements, and high‐pressure synthesis in polynitrides, expanding the knowledge for the development of advanced energy materials 
    more » « less