Cyclic stability is the ability of an electrode, a device or a material to retain its performance over repeated charge-discharge or load-unload cycles, and it is reported as the fraction of the initial capacity or property remaining after a stated number of cycles at a stated rate. In batteries the loss is rarely due to one cause: the active material may transform or dissolve, the electrode may lose electrical contact as particles move apart, and the electrolyte may be consumed in side reactions that thicken the interphase. Conversion and alloying electrodes undergo the largest volume change, and embedding the active phase in a carbon matrix is the standard way to accommodate it, iron oxide in a carbon microsphere being an early example [1]. A conductive scaffold performs the same function in a silicon electrode, where a nanowire network keeps the particles connected through repeated expansion [2], and controlling the pore structure of the electrode gives the same gain more generally [3]. In lithium-sulfur cells the loss mechanism differs, because the intermediate polysulfides dissolve and migrate, so the sulfur is encapsulated in a shell [4]. Binding it into a conductive polymer network is the alternative [5]. Reported retention figures depend strongly on the rate and the depth of discharge, so they are comparable only under matched conditions.