A program in the Department of Mechanical Aerospace and Nuclear Engineering (MANE)

   
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PYROELECTRIC ACCELERATION


 

Introduction
Experiments
           Electrons and ions
           X-rays production
Neutron production
Publications

A paired  pyroelectric crystal x-ray generator in action

A Pair of pyroelectric crystals in action.
Red - electrons and blue - x-rays.

 

 

INTRODUCTION

This research is focused on understanding the pyroelectric effect in order to use it to effectively accelerate electrons and ions. The accelerated electrons and ions can be used to produce beams of electrons, ions, x-rays, and possibly monoenergetic neutrons and gamma rays. The first application of the pyroelectric effect for x-ray production was reported by Brownridge. The first commercial compact x-ray source was manufactured by Amptek. The goal of our research is to further develop this technology in order to achieve higher acceleration potential and current. Such improvements will allow us to use this technology to create useful highly compact, battery operated, high energy x-rays, and neutron sources.

Theory of Operation

Pyroelectric crystals are spontaneously polarized along an axis. In other words, they have a bulk dipole moment that exists in equilibrium conditions and does not sum to zero over the volume of the crystal. This polarization is usually masked by the gradual accumulation of surface charges.   The distinguishing trait of pyroelectric crystals is that the polarization of the crystal is altered dramatically with changes in the temperature of the crystal, such that the polarization is no longer masked and a large voltage can be observed across the crystal.

The pyroelectric effect allows to easily achieve very high electric potentials by heating a small (~4mm x 4mm x 4mm) crystal in a low-pressure (0.5-10 mTorr) environment. We successfully used this effect to demonstrate production of x-rays with energies up to 200 keV.

EXPERIMENTS

Most of the work is done with LiTaO3 but some was also done with LiNbO3. The crystals range in thickness from 1 to 10 mm with typical area of 14-25 mm2. During operation, the crystals are maintained in a vacuum chamber with a pressure of 0.5-10 mTorr. The crystals are heated to about 160 ºC and the measurements are done during the crystal heating or cooling phases. Most of the emissions occur at temperatures above 30 ºC.

Electrons and ions

Several measurements were done using a surface barrier detector to directly detect electrons and ions.  A typical electron spectrum and ion spectra are shown in figures 1 and figure 2. The electron spectrum is obtained during a cooling cycle with Z- side of the crystal is facing the surface barrier detector. The ion spectrum is obtained by revering the crystal polarity such that during the cooling cycle the Z+ is facing the detector. The spectrum in figure 1(a) shows unique pileup peaks, calculations indicates that this pileup is much higher than what is expected from random coincidence pile-up. This gives an indicates on the "bunched" nature of the electron emission from these crystals.

(a)

(b)

Figure 1 – Typical electron spectrum from a single LiTaO3 crystal, measured using a surface barrier detector (a) pileup spectrum (b) high energy spectrum

  

Figure 2 – Typical ion spectrum obtained during cooling of a LiTaO3 crystal with the Z+ facing the detector.

X-ray Production

When accelerate electrons hit the crystals or other metallic targets bremsstrahlung and characteristic X-rays are produced. These photons are detected using an Amptek x-ray detector XR-100CDT. We examined the possibility of multiplying the acceleration potential by using two pyroelectric crystals. Figure 3 shows the geometry of such an experiment with paired crystals and Figure 4 shows the typical spectrum, A 6 mm thick SST absorber was used in order to reduce the low energy x-ray rate.

Figure 3 –paired crystal system.

 

Figure 4 – The x-ray spectrum sum from 5 cooling cycles.

 

Such spectrum has high enough energy to fluoresce lead and thorium. The geometry use to demonstrate thorium fluorescent is shown in Figure 5; such geometry utilized the pyroelectrically generated x-rays to fluoresce the thorium sample in transmission geometry and the spectrum obtained is shown in figure 6. In this case the sample is radioactive and will fluoresce by excitations from the radioactive decay. This emission is treated as background, figure 6 shows the background and the pyro-x-rays induced fluorescent.

Figure 5 – The geometry used for lead florescent measurement.

 


Figure 6 – x-ray florescent spectrum from thorium.

 

 Lead fluorescet was done in a “reflection” geometry and the results are show in Figure 7.

 

Figure 7 – x-ray florescent spectrum from lead.

 

NEUTRON PRODUCTION

Neutron production from such device is now under investigation. The idea is to use a paired crystal accelerator with a low pressure fille (5-20 mTorr) of D2 gas. In addition to the gas we would use a deuterium enriched target (such as deuterated plastic). The deuterium will be accelerated towards the deuterated target and if the right conditions exist, a D-D reaction will take place. This reaction is accompanies by a 2.5 MeV neutrons that can be detected outside the vacuum chamber. This type of accelerator can also be used on a target containing tritium to obtain a higher yield of D-T neutrons with energy of 14 MeV.
Check our latest publication below which provides all the details of our neutron generator.

This figure shows the neutron output from our "Doubel Crystal Fusion" device. The neutron spectrum is measured using a liquid scintilator. The spectrum was calcibrated using gamma sources and thus the x-axis energy is given in units of recoiled electron energy.

 

PUBLICATIONS

Jeffrey Geuther, Yaron Danon, Frank Saglime, Bryndol Sones, "Electron Acceleration for X-ray Production Using Paired Pyroelectric Crystals", abstracts of the sixth International Meeting on Nuclear Applications of Accelerator Technology, AccApp’03, p. 124, San Diego, June 1-5, 2003

Jeffrey Geuther and Yaron Danon, "Increasing X-Ray Energy By Paring Pyroelectric Crystals", (Invited), 18th International Conference on the Application of Accelerators in Research and Industry (CAARI 2004), Ft Worth TX, October 10-15, 2004.

Jeffrey A. Geuther, Yaron Danon," Pyroelectric Electron Acceleration: Improvements and Future Applications", ANS Winter Meeting Washington, D.C, November 14 – 18, 2004.

Jeffrey A. Geuther, Yaron Danon, "Electron and Positive Ion Acceleration with Pyroelectric Crystals", J. Appl. Phys. 97, 074109 (2005).

Jeffrey A. Geuther, Yaron Danon, "High-Energy X Ray Production with Pyroelectric Crystals", J. Appl. Phys. 97, 104916 (2005).

Jeffrey Geuther, Yaron Danon and Frank Saglime, “Nuclear reactions induced by a pyroelectric accelerator”, Physical Review Letters, 96 054803 (2006).

Media Coverage of "Double Crystal Fusion"

"RPI claims battery-fueled, room-temp fusion", EETimes, 02/20/2006.

"Double Crystal Fusion' Could Pave The Way For Portable Device", Science Daily, February 14, 2006.

"Tabletop nuclear fusion device developed", Physorg.com, February 13, 2006.

This research is sponsored in part for DOE NEER grant no. 04ID14596