In contrast to normal diffusion processes, thermal conduction in one-dimensional systems is anomalous. The thermal conductivity is found to vary with the length as
κ∼Lα(α>0), but there is a long-standing debate on the value
α. Here, we present a canonical example of this behavior in polymer-grafted spherical nanoparticle (GNP) melts at fixed grafting density and nanoparticle radius. For long chains (chain length
N≥945), the experimental
κ(N) of GNP melts decreases with
N, i.e., polymer concentration. For
N<945, however,
κ(N) unexpectedly increases with
N with a maximum near
N∼945. For these systems, the extensional free energy per polymer chain is predicted to be maximized near
Nmax≈940 for
σ≈0.47 chains/nm2, which indicates the dominance of extended conformations at short
N and Gaussian-like conformation for longer
N. In the former regime, the thermal conductivity of extended polymer chains increases with
N and follows
κp∼Ndry0.46±0.02, which provides experimental evidence of a novel class of superdiffusive thermal transport with
α=1/2. Published by the American Physical Society 2024