We demonstrate that migration away from self-produced chemicals (chemorepulsion) generates a generic route to clustering and pattern formation among self-propelled colloids. The clustering instability can be caused either by anisotropic chemical production, or by a delayed orientational response to changes of the chemical environment. In each case, chemorepulsion creates clusters of a self-limiting area which grows linearly with self-propulsion speed. This agrees with recent observations of dynamic clusters in Janus colloids (albeit not yet known to be chemorepulsive). More generally, our results could inform design principles for the self-assembly of chemorepulsive synthetic swimmers and/or bacteria into nonequilibrium patterns. DOI: 10.1103/PhysRevLett.115.258301 PACS numbers: 82.70.Dd, 05.65.+b, 82.40.Ck, 87.17.Jj Active systems, such as suspensions of autophoretic colloidal swimmers, motile bacteria, or other self-propelled particles, are far from equilibrium even in steady state due to their continuous energy expenditure [1,2]. Unlike isothermal Brownian colloids, motile particles can accumulate in regions where they move more slowly. They also slow down at high density, creating a positive feedback loop that can lead ultimately to motility-induced phase separation (MIPS) [3,4].Experiments with artificial self-propelled colloids have reported self-organized dynamic clustering, sometimes at densities well below that expected to trigger MIPS [5,6]. These "living clusters" seem to reach a limiting size and do not coarsen indefinitely: they show microphase separation rather than macrophase separation as in MIPS. So far, the underlying mechanism remains unclear.In such experiments, motility is autophoretic: a chemical reaction is catalyzed on part of the colloid surface, creating a gradient of reagent and/or product that drives the particle forward by diffusiophoresis or a similar mechanism [7-9]. The same gradients can then cause chemically mediated long-range interactions between the colloids, and can also cause rotational torques that bias the swimming direction up or down the chemical gradient (an effect known as chemotaxis) [10,11]. This fact has suggested a parallel between the experiments in Ref. [5] and the Keller-Segel (KS) model [12][13][14] for microorganisms interacting via chemical signaling. This mapping, which assumed that active colloids swim up chemical gradients (the "chemoattractive" case), can explain clustering, but leads to complete phase separation, rather than a self-limiting cluster size. A combination of a passive drift up the chemical gradient and self-propulsion down it ("chemorepulsion") might lead to finite size clusters [15]; however, at variance with experiments [5,16], these should shrink as the self-propulsion speed increases [15]. A more general study of chemoresponsive active colloids in the limit of fast chemical dynamics suggests a far larger potential for pattern formation than is predicted by the KS model [10].Here we propose a theoretical framework for active colloids...