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Most current highly efficient organic solar cells utilize small molecules like Y6 and its derivatives as electron acceptors in the photoactive layer. In this work, a small molecule acceptor, SC8-IT4F, is developed through outer side chain engineering on the terminal thiophene of a conjugated 6,12-dihydro-dithienoindeno[2,3-d:2',3'-d']-s-indaceno[1,2-b:5,6-b']dithiophene (IDTT) central core. Compared to the reference molecule C8-IT4F, which lacks outer side chains, SC8-IT4F displays notable differences in molecule geometry (as shown by simulations), thermal behavior, single-crystal packing, and film morphology. Blend films of SC8-IT4F and the polymer donor PM6 exhibit larger carrier mobilities, longer carrier lifetimes, and reduced recombination compared to C8-IT4F, resulting in improved device performance. Binary photovoltaic devices based on the PM6:SC8-IT4F films reveal an optimal efficiency over 15%, which is one of the best values for non-Y type small molecule acceptors (SMAs). The resultant devices also show better thermal and operational stability than the control PM6:L8-BO devices. SC8-IT4F and its blend exhibit a higher relative degree of crystallinity and π coherence length, compared to C8-IT4F samples, beneficial for charge transport and device performance. The results indicate that outer side chain engineering on existing small electron acceptors can be a promising molecular design strategy for further pursuing high-performance organic solar cells., (© 2025 The Author(s). Advanced Science published by Wiley‐VCH GmbH.)