“…Since the specific values of activation energies of forward dissociation, E F , reverse annealing, E R , and diffusion coefficient, E D , were unknown, the inconsistency between time-exponent n and temperature activation E A was initially not highlighted. However, generalized scaling arguments consistently showed that E A $ E D /n [1,4], with E F $ E R [1,2,4,28]. The measured E A therefore provided a direct measure of E D $ 0.5-0.6 eV, which in turn implicated H 2 diffusion [29]!…”