Conducting polymers, despite their promising electrochromic properties, face limitations in smart windows due to their inverse modulation in visible and near-infrared (NIR) regions. In this study, we introduce novel "black-to-black" electrochromic copolymers, synthesized through direct arylation polymerization (DArP) of tris(thienothiophene) (TTT), 3,4dialkylthiophene (DKTh), and benzo[c][1,2,5]thiadiazole (Tz) monomers. These copolymers demonstrate minimal visible impact (<5%) and broad NIR modulation (>60%). The resulting electrochromic devices seamlessly transition between "Warm" mode (low visible and high NIR transmittance) and "Dark" mode (low visible and NIR transmittance), showcasing high switching stability, open-circuit memory, and coloration efficiency. The synthesized copolymers and devices surpass conventional "color-to-transmissive" conducting polymers, exhibiting significant solar heat gain coefficient (SHGC) modulation and high optical contrast. This discovery prompts further exploration of dual-band electrochromic materials, particularly those featuring a "Warm" mode based on conducting polymers.