New approaches for area-selective deposition (ASD) are becoming critical for advanced semiconductor patterning. Atomic layer deposition (ALD) and atomic layer etching (ALE), that is, "inverse ALD", are considered important for ASD, but to date, direct integration of ALD and ALE for ASD has not been reported. This work demonstrates that self-limiting thermally driven ALE, using WF 6 and BCl 3 , can be directly coupled with selflimiting thermal ALD, using TiCl 4 and H 2 O, in a single isothermal reactor at temperature <200 °C to achieve ASD of TiO 2 thin films on common Si/SiO 2patterned surfaces without the use of organic nucleation inhibitors. We show that ALD/ALE "supercycles" (where one supercycle comprises, e.g., 30 ALD cycles followed by 5 ALE cycles) can be reliably repeated to yield more than 12 nm of TiO 2 while maintaining a selectivity fraction S > 0.9, nearly a 10× improvement over previous reports of inherent TiO 2 ASD. After ALD/ALE (=30/5) 14 supercycles at 170 °C, X-ray photoelectron spectroscopy data show a small Ti 2p signal on Si−H (hydrogen fluoride-cleaned Si), with no Ti 2p signal detected after additional "postetch" ALE cycles. At 150 °C, extended supercycles lead to unwanted particles visible by electron microscopy, which is ascribed to the formation of unreactive mixed silicon/titanium oxide nuclei. The number density of visible particles is consistent with modeled film growth trends. Overall, this work provides new insights into the capabilities for ASD of dielectric materials and a starting point to realize more complex atomic-scale processes using ALD, ALE, and other self-limiting reaction schemes.