Two A(2)-D-A(1)-D-A(2)-type small molecule acceptors (SMAs), DFB-dIDT and BT-dIDT with 2,5-difluorobenzene (DFB) or benzothiadiazole (BT) as electron-withdrawing core (A(1)) and a derivative of indanone as A(2) units, were prepared for applications in organic solar cells (OSCs). The results indicate that BT unit is more beneficial to forming multiple noncovalent conformational locks of N center dot center dot center dot S and N center dot center dot center dot H between BT and IDT unit than DFB in the core, so BT-dIDT showed better molecular coplanarity, higher-lying HOMO energy level, more red-shifted spectrum, superior molar absorption coefficient (1.60 x 10(5) M-1 cm(-1) at 696 nm), more complementary absorption spectrum with PBDB-T and better photovoltaic performance than DFB-dIDT. As a result, the BT-dIDT-based OSCs blending with PBDB-T exhibited higher power conversion efficiency (PCE) value of 10.52% with higher J(sc) of 18.59 mA cm(-2) than that of the DFB-dIDT-based devices (PCE of 6.71% with J(sc) of 15.58 mA cm(-2)). These results demonstrate that the A(2)-D-A(1)-D-A(2)-type SMAs incorporated with a suitable electron-deficient core are promising candidates for high performance OSCs.