Molecular doping allows enhancement and precise control of electrical properties of organic semiconductors, and is thus of central technological relevance for organic (opto‐) electronics. Beyond single‐component molecular electron acceptors and donors, organic salts have recently emerged as a promising class of dopants. However, the pertinent fundamental understanding of doping mechanisms and doping capabilities is limited. Here, the unique capabilities of the salt consisting of a borinium cation (Mes₂B⁺; Mes: mesitylene) and the tetrakis(penta‐fluorophenyl)borate anion [B(C₆F₅)₄]⁻ is demonstrated as p‐type dopant for polymer semiconductors. With a range of experimental methods, the doping mechanism is identified to comprise electron transfer from the polymer to Mes₂B⁺, and the positive charge on the polymer is stabilized by [B(C₆F₅)₄]⁻. Notably, the former salt cation leaves during processing and is not present in films. The anion [B(C₆F₅)₄]⁻ even enables the stabilization of polarons and bipolarons in poly(3‐hexylthiophene), not yet achieved with other molecular dopants. From doping studies with high ionization energy polymer semiconductors, the effective electron affinity of Mes₂B⁺[B(C₆F₅)₄]⁻ is estimated to be an impressive 5.9 eV. This significantly extends the parameter space for doping of polymer semiconductors.