personally we have tried to setup a neutron diffraction scattering but unfortunately until now we had no chance to do it. Inside Pd lattice there are two possible sites, Octahedral and Tetrahedral, just for hypotetical example if you fill all the Oct sites you have PdH then filling the Tet sites you will achieve PdH3. What is really happen is that you cannot fill all the Oct, but at about 60% of Oct filling, H start to fill Tet sites.
Have you suggestion to measure the crystal structure of PdH?
I have an access rather easy to neutron diffraction at the ILL. But the sample must be D-charged (not with H, you know). In the past I had also used in-situ high pressure experiment at ESRF.
In fact you know that, according to the Fukai's technique it is possible to transform PdHx (x
sorry for delay but its a very busy period this one. I know you was working with Fukai, I was working for one year in Japan in the special project NHE.
usually I produced wire samples to be measured with SQUID's and I can even produce tape samples let say 4mm x 10mm x 0.1mm.
Let me know how we can go forward with the understanding.
I don't know if we produce SAV in the PdHx sample, but as you explained, the energy of insertion is important but another important parameter is the insertion time, then the volume and shape of the sample.