carrier back-scattering remains suppressed and the electrical transport is dominated by high-energy carriers that favorably affect the thermopower of Cd 3 As 2 . [ 9 ] Since the power factor is to increase with the carrier mobility, µ , and weighted density-ofstates effective mass, i.e., S 2 σ ≈ µ D *1.5 m , and the lattice thermal conductivity is predicted to be very low, Cd 3 As 2 shows a strong potential for demonstrating high, device-favorable S , and in turn ZT , Table 1 . [ 10 ] Binary cadmium arsenide that solidifi es as Cd 3 As 2 is known to undergo multiple polymorphic solid-solid transitions β α α α → ′′ → ′ → at T of 578, 475, and 225 °C, respectively; the latter of which limits the growth temperature to 225 °C. Given the melting point of this compound of 721 °C, melt-based crystal growth techniques have to be ruled out from consideration. Pulsed-laser evaporation was offered as an alternative route, [ 17 ] but the resultant samples show highly reduced, i.e., polycrystalline and amorphous quality.In this work, a low-T chemical-vapor deposition route is used instead to grow platelets up to cm size in Cd 3 As 2 in a horizontally oriented hot-wall atmospheric pressure chemical vapor deposition (CVD) reactor. To lower the residual pressure of oxygen and water vapors, the reactor was initially fl ushed several times by bringing the base pressure down to ≈1 m Torr and refi lling it with 99% pure argon gas. The temperature of the furnace was gradually ramped up from ≈25 to 700 °C (measured at the middle point of the quartz tube) within an hour. Pure, polycrystalline Cd 3 As 2 chunks were used as a precursor, while quartz and alumina wafers served as growth substrates. To facilitate vapor transport of Cd and As, a steady argon fl ow was maintained within the reactor with the rate of ≈0.2 SCCM. The growth duration was set not to exceed 3 h. Upon completion, the heater was shut down and the reactor was left to cool down naturally at the average rate of ≈5 °C min −1 in the presence of argon fl ow. Except for the tube end points, the temperature gradient (as probed with the help of IR temperature sensor) along the tube main axis, T ∇ was on average a few degrees per cm, Figure 1 , top.After the growth, the substrate as well as the reactor sidewalls was subject to visual and optical microscope inspections, Thermoelectric generators (TEGs) directly convert thermal into electrical energy and are the prime candidates for application in low-grade thermal energy/heat waste recovery. These solidstated devices demonstrate several critical advantages over other power generators as they are silent, very reliable, and compact/lightweight, which make them attractive for several niche deployments including transportation, space satellites, electronics cooling, and thermovoltaic cells. [1][2][3] Yet, TEGs with typical effi ciency of only ≈5%-8% demonstrate poor effi ciencyto-cost ratio, and the problem stems mainly from the poor conversion characteristics of the thermoelectric (TE) materials themselves.The TE performance is rou...