bonds. [18,19] The formation of hydrogen bonds reduces the coulombic interactions between lead and bromide ions, and then ammonium ligands will fall off from the QD surface along with bromide ions (Scheme 1a left). [20] On the other hand, the deprotonated ammonium ligands cannot interact with the CsPbBr 3 QDs.Therefore, the use of a single ligand without amine groups and reversible processes could overcome the purification stability problem, as shown recently by Yassitepe et al, who developed an aminefree method using only oleic acid (OA) as ligands. [21] The resulting CsPbBr 3 QDs could be washed several times without size increase or emission shift (Scheme 1a middle); however, the QY of these QDs was relatively low and the long-term stability was poor. The low QY results from the presence of enormous surface bromide vacancies (V Br ), since V Br exhibited obvious negative exciton trapping effect (Scheme 1b middle). [22] The groups of both Xia and Alivisatos recently confirmed the effect of V Br in their very recent works and near 100% QY can be achieved swimmingly by compensating Br ions with any bromides during or after synthesis (Scheme 1b left). [23,24] Hence, it seems contradictory that considering the QY, surface V Br should be avoided, while on account of good stability, ammonium which interacts with Br atoms should be excluded. To reduce the V Br density and reversible protonation, Kovalenko et al. introduced several kinds of zwitterionic ligands. [15,25] CsPbBr 3 QDs maintained high QY values of ≈80% and exhibited good purification stability. However, the preparation procedures were complicated, and even required precursor synthesis. Tan et al. reported the preparation of highly luminescent and stable CsPbBr 3 QDs prepared with addition of octylphosphonic acid (OPA). [26] However, in addition to OPA, the preparation also required the introduction of OA and trioctylphosphine oxide (TOPO), complicating the mechanism because TOPO and OA can also passivate and efficiently stabilize the CsPbBr 3 surface. [27,28] Additionally, OPA is insoluble in octadecene and is unable to dissolve PbBr 2 without TOPO. [29] In this work, we propose a concept of equivalent ligand, hypothesizing that if a ligand can play a role similar to Br ions to a certain extent and form strong interaction with lead ions (surfactant), then the problems of V Br and weak interaction can be solved simultaneously. The simplest source of Br ions is HBr, andThe stability and optoelectronic device performance of perovskite quantum dots (Pe-QDs) are severely limited by present ligand strategies since these ligands exhibit a highly dynamic binding state, resulting in serious complications in QD purification and storage. Here, a "Br-equivalent" ligand strategy is developed in which the proposed strong ionic sulfonate heads, for example, benzenesulfonic acid, can firmly bind to the exposed Pb ions to form a steady binding state, and can also effectively eliminate the exciton trapping probability due to bromide vacancies. From these two aspects, the s...