Abstract
Using the large (≈ 100 GHz) hyperfine coupling of the Tl2+ (6s1) ion as a spin probe, we have investigated the evolution of glassy behavior in (NH4) xRb1−xH2 PO4 single crystals. Also reported is a microwave dielectric loss determination of the phase diagram of (ND4) xRb1−xD2AsO4. The glass formation temperature, Tc, is found to be significantly higher and the glass phase range narrower in the deuterated arsenate system than in the corresponding protonated arsenate system. Both of these phenomena are tentatively interpreted in terms of a random bond version of the Ising model in a transverse tunneling field.