Cluster owner: Vantasner AG device program. Records compiled from the published literature, search date 2026-10-21. Every row lists a real publication with authors, venue, year, and DOI where one exists. Scope note: cavitation and ultrasound records are held in 02-ultrasound-sonofusion.md; this file covers the electrochemical co-deposition line and Navy-affiliated calorimetry. The rock-fracture piezonuclear line is held in 08-piezonuclear-fracto-fusion.md.
Records
| # | Who | When | Venue / DOI | Setup | Materials | Loading | Excitation | Conditions | Reported outputs |
|---|---|---|---|---|---|---|---|---|---|
| 1 | M. H. Miles, R. A. Hollins, B. F. Bush, J. J. Lagowski, R. M. Priest (China Lake naval laboratory, California) | 1993 | Journal of Electroanalytical Chemistry 346(1-2), 99-117; DOI 10.1016/0022-0728(93)85006-3 | Isoperibolic electrochemical calorimetry, closed cells, gas sampling | Palladium cathodes, LiOD in D2O, LiOH in H2O | loading tracked per cell by cathode resistance | direct-current (DC) electrolysis, high current density | D2O cells run against paired H2O cells | Excess power in D2O cells and none in H2O cells; gas samples taken during excess-power episodes carry higher helium-4 levels; helium rate near 1e11 atoms per second per watt |
| 2 | S. Szpak, P. A. Mosier-Boss, J. J. Smith (Space and Naval Warfare Systems Center, SPAWAR, San Diego) | 1994 | Journal of Electroanalytical Chemistry 379(1-2), 121-127; DOI 10.1016/0022-0728(94)87130-2 | Electrochemical co-deposition with in-situ uptake monitoring | PdCl2 plus LiCl in D2O plated onto substrate electrodes | deuterium uptake measured during film growth | DC plating current | potentiostatic control | Palladium deuteride forms as it is deposited; the film loads deuterium while it grows |
| 3 | S. Szpak, P. A. Mosier-Boss, J. J. Smith | 1996 | Physics Letters A 210(6), 382-390; DOI 10.1016/0375-9601(95)00915-9 | Co-deposition cell paired with radiation search on film | same plating bath; nickel-screen cathode, film in sealed envelopes | not restated here | DC plating | about 12 h runs | Film exposures localized at the cathode; authors propose a low-energy radiation source; tritium enrichment of the electrolyte reported in the same series |
| 4 | S. Szpak, P. A. Mosier-Boss, R. D. Boss, J. J. Smith | 1998 | Fusion Technology 33(1), 38-51; DOI 10.13182/FST98-A14 | Co-deposition cells with tritium assay and mass-balance analysis | PdCl2 plus LiCl in D2O | not restated here | DC plating | multi-run series; sporadic timing | Tritium production reported, sporadic, at an estimated 1e3 to 1e4 atoms per second; burst-like events separated by inactive periods |
| 5 | S. Szpak and P. A. Mosier-Boss (editors) | 2002 | SPAWAR Systems Center San Diego Technical Report 1862, two volumes (Thermal and Nuclear Aspects of the Pd/D2O System, Vol. 1: A Decade of Research at Navy Laboratories; Vol. 2: Simulation of the Electrochemical Cell (ICARUS) Calorimetry) | Program review plus a numerical cell-calorimetry model | the full Navy Pd/D record to 2002 | as per constituent studies | as per constituent studies | Navy laboratory protocols | Consolidated heat and nuclear-product record; the ICARUS code simulates the cell thermal response |
| 6 | S. Szpak, P. A. Mosier-Boss, M. H. Miles | 1999 | Fusion Technology 36(2), 234-241; DOI 10.13182/FST99-A105 | Co-deposition calorimetry with infrared scanning of the cathode | co-deposited Pd/D films | not restated here | DC plating | runs of several days | Excess power with reproducibility across runs; thermal instabilities; local hot spots visible in infrared images |
| 7 | M. H. Miles, S. Szpak, P. A. Mosier-Boss, M. Fleischmann | 2004 | Thermochimica Acta 410(1-2), 101-107; DOI 10.1016/S0040-6031(03)00401-5 | Dewar-style calorimetry of co-deposition electrodes | co-deposited Pd/D electrodes | not restated here | DC electrolysis | Fleischmann-Pons class Dewar protocol | Sustained excess power reported; thermal behavior analyzed with the Fleischmann-Pons calorimetry formalism |
| 8 | S. Szpak, P. A. Mosier-Boss, C. Young, F. E. Gordon | 2005 | Naturwissenschaften 92(8), 394-397; DOI 10.1007/s00114-005-0008-7 | Operating Pd/D2O cell with the cathode in an external electrostatic field | Pd/D2O cell with lithium and chloride electrolyte, platinum auxiliary electrode | not restated here | external electrostatic field plus electrolysis | reproducible protocol described in the paper | Discrete sites with molten-like surface features; elements including aluminum, magnesium, calcium, silicon and zinc present on those sites |
| 9 | S. Szpak, P. A. Mosier-Boss, C. Young, F. E. Gordon | 2005 | Journal of Electroanalytical Chemistry 580(2), 284-290; DOI 10.1016/j.jelechem.2005.03.039 | Co-deposited film morphology under an external electric field | co-deposited Pd/D films | not restated here | external electric field plus plating | microscopy of deposited films | External field changes the surface morphology at discrete sites |
| 10 | S. Szpak, P. A. Mosier-Boss, F. E. Gordon | 2007 | Naturwissenschaften 94(6), 511-514; DOI 10.1007/s00114-007-0221-7 | Co-deposition with CR-39 track foils at the cathode, external fields | CR-39 foils (polyallyl diglycol carbonate track detector) | not restated here | electrostatic or magnetostatic field plus electrolysis | reproducible runs; track density reported above controls | Charged-particle tracks on CR-39; the authors propose an electron-capture model |
| 11 | P. A. Mosier-Boss, S. Szpak, F. E. Gordon, L. P. G. Forsley | 2007 | The European Physical Journal Applied Physics 40(3), 293-303; DOI 10.1051/epjap:2007152 | CR-39 method paper for co-deposition cells | CR-39 in contact with the cathode region | not restated here | electrolysis | control experiments and artifact tests | Pits matching nuclear-origin morphology; the authors report exclusion of radionuclide contamination, bubble impingement and chemical attack |
| 12 | P. A. Mosier-Boss, S. Szpak, F. E. Gordon, L. P. G. Forsley | 2009 | Naturwissenschaften 96(1), 135-142; DOI 10.1007/s00114-008-0449-x | CR-39 in close contact with the co-deposition cathode | CR-39 at the cathode | not restated here | electrolysis | cathode-contact geometry | Triple tracks diagnostic of the carbon breakup reaction 12C(n,n')3-alpha; the authors infer neutrons of 9.6 MeV or more |
| 13 | P. A. Mosier-Boss, S. Szpak, F. E. Gordon, L. P. G. Forsley | 2009 | The European Physical Journal Applied Physics 46(3), 30901; DOI 10.1051/epjap/2009067 | Spacer experiments and track modeling on CR-39 | CR-39 with spacer layers | not restated here | electrolysis | energy and geometry analysis | Track geometry and particle energetics characterized; the effect of water on the particles discussed |
| 14 | P. A. Mosier-Boss, J. Dea, L. Forsley, M. Morey, J. Tinsley, J. Hurley and co-workers | 2010 | The European Physical Journal Applied Physics 51(2), 20901; DOI 10.1051/epjap/2010087 | Side-by-side comparison of co-deposition CR-39 against a deuterium-tritium (DT) neutron source | CR-39; DT neutron generator | not restated here | DT-source calibration plus electrolysis | matched etch and read conditions | Co-deposition triple tracks compared against DT-generated triple tracks; the authors report agreement in character |
| 15 | P. A. Mosier-Boss, J. Dea, F. E. Gordon, L. P. G. Forsley, M. H. Miles | 2011 | Journal of Condensed Matter Nuclear Science (JCNS) 4; DOI 10.70923/001c.72134 | Twenty-year review of the co-deposition program | the full co-deposition record | as per constituent studies | as per constituent studies | laboratory series 1991 to 2011 | Consolidated record of excess heat, tritium, charged particles and transmutation reports |
| 16 | P. A. Mosier-Boss | 2012 | JCNS 6; DOI 10.70923/001c.72168 | Review of nuclear products reported in the field | heat, helium-4, tritium, charged particles, X- and gamma rays, transmutation products | as per constituent studies | as per constituent studies | field-wide survey | Catalog of the reported nuclear products and their measurement methods |
| 17 | A. Savrasov, V. Prokopenko, E. Andreev | 2017 | JCNS 22; DOI 10.70923/001c.72415 | Independent replication of the GALILEO Project co-deposition cells | CR-39 plus co-deposition cells | not restated here | electrolysis | four experiments | Two of the four runs show excess alpha-track density on CR-39 against background detectors |
| 18 | P. A. Mosier-Boss, F. E. Gordon, L. P. G. Forsley, D. Zhou | 2017 | International Journal of Hydrogen Energy 42(1), 416-428; DOI 10.1016/j.ijhydene.2016.09.223 | CR-39 method paper, part 1: microscopy, automated scanning, LET analysis | CR-39 | not restated here | as per source runs | detector characterization | Track-analysis workflow: linear energy transfer (LET) sorting of particle populations |
Record note: the CR-39 track interpretation received a published comment by L. Kowalski (The European Physical Journal Applied Physics 44(3), 287-290, 2008; DOI 10.1051/epjap:2008161) and an authors' response (44(3), 291-295, 2008; DOI 10.1051/epjap:2008182). Both are part of the record; the response adds spacer data in support of the original assignment.
Narrative
The Navy line begins at SPAWAR San Diego, where Stan Szpak and Pamela Mosier-Boss inverted the Fleischmann-Pons geometry: instead of loading a bulk palladium rod for days, they grow the palladium and load it with deuterium at the same time, co-depositing palladium from a bath of palladium chloride and lithium chloride in heavy water while deuterium evolves at the cathode. The electrode is always fresh, always expanding, and never needs a long charge-up. This one idea made the phenomenon addressable by any laboratory with a beaker, a power supply and discipline, and it is the direct ancestor of our own plan to run freshly loaded hydride particles inside the working fluid.
Melvin Miles at the China Lake naval laboratory carried the calorimetry side. His 1993 paper pairs every deuterium cell with a light-water cell and reports excess power only on the deuterium side, together with helium-4 in the gas headspace at the 1e11 atoms per second per watt scale. He then joined the SPAWAR group and put co-deposition electrodes into Fleischmann-Pons class Dewar calorimeters (1999, 2004). The group's summaries emphasize reproducibility of the heat signal, infrared images of hot spots on the cathode, and thermal instabilities that the authors call mini-explosions. In one paper the birth and death of hot spots is tracked by infrared imaging while a piezoelectric substrate glued to the electrode registers voltage spikes at the same moments, which is, for our purposes, a lovely precedent: a piezo element doubling as an event sensor.
The nuclear-product record grew in stages: tritium (1998, sporadic, 1e3 to 1e4 atoms per second), then CR-39 track foils pressed against the cathode under external electric and magnetic fields (2005 to 2010), with the triple-track carbon-breakup signature offered as a neutron fingerprint and calibrated against a deuterium-tritium generator. Independent work exists: the 2017 JCNS replication reports excess alpha-track density in two of four runs. The field also produced a published exchange on track interpretation (Kowalski 2008 and the authors' response), which is precisely why our device carries time-of-flight neutron counters alongside CR-39: two independent detector classes that must agree before we call anything.
The operational signature across fifteen years of records is sporadicity. Heat, tritium and tracks arrive in bursts separated by quiet periods, and the reported loadings sit near the electrochemical limit of about D/Pd 0.7 to 1 (field-wide figure). A device that expects bursts needs long runs, time-stamped logging on every channel, and thermal headroom for positive-feedback excursions.
Carry into device
- Adopt the co-deposition principle as our in-situ loading fallback: reference bath 0.05 M palladium chloride plus 0.3 M lithium chloride in D2O, plated onto substrate grains or screens, to grow fresh, defect-rich PdD immediately before a run if pre-loaded powder ages.
- Copy the paired-control discipline: every deuterated configuration runs its hydrogen analog in the same fixture, the way China Lake paired D2O with H2O cells; helium-4 headspace assay with a mass spectrometer at the 1e11 atoms per second per watt yardstick.
- CR-39 foils in open-and-masked pairs plus spacer stacks, pressed against the suspension vessel, with a deuterium-tritium generator calibration set of the kind used in the 2010 comparison; track reading by the automated LET workflow of the 2017 method paper.
- Infrared imaging of the active volume plus piezo-wafer spike listening: our suspension already contains piezoelectric grains, so we read the same grains as event sensors, following the SPAWAR mini-explosion readout.
- Dewar and isoperibolic calorimeters in redundant combination, with the cell simulated numerically before construction (the ICARUS precedent of Technical Report 1862).
- Design for sporadic, burst-like kinetics: multi-day runs, burst-tolerant time-stamped data capture on all channels, and power supplies rated for the positive-feedback excursions the record describes.
- Expect loading near D/Pd 0.7 to 1 for electrochemical palladium and do not plan beyond it; our titanium and zirconium deuterides are there to raise deuteron density instead.