Structural phase-change materials are of great importance for applications in information storage devices. Thermally driven structural phase transitions are employed in phase-change memory to achieve lower programming voltages and potentially lower energy consumption than mainstream nonvolatile memory technologies. However, the waste heat generated by such thermal mechanisms is often not optimized, and could present a limiting factor to widespread use. The potential for electrostatically driven structural phase transitions has recently been predicted and subsequently reported in some two-dimensional materials, providing an athermal mechanism to dynamically control properties of these materials in a nonvolatile fashion while achieving potentially lower energy consumption. In this work, we employ DFT-based calculations to make theoretical comparisons of the energy required to drive electrostatically-induced and thermally-induced phase transitions. Determining theoretical limits in monolayer MoTe 2 and thin films of Ge 2 Sb 2 Te 5 , we find that the energy consumption per unit volume of the electrostatically driven phase transition in monolayer MoTe 2 at room temperature is 9% of the adiabatic lower limit of the thermally driven phase transition in Ge 2 Sb 2 Te 5 . Furthermore, experimentally reported phase change energy consumption of Ge 2 Sb 2 Te 5 is 100-10,000 times larger than the adiabatic lower limit due to waste heat flow out of the material, leaving the possibility for energy consumption in monolayer MoTe 2 -based devices to be orders of magnitude smaller than Ge 2 Sb 2 Te 5 -based devices.