als as candidates are considered and developed to replace Pt CE, such as sulphide [6,7], nitride [8], polymer [9], carbon materials [5,10,11], and hybrid materials [12].Low-cost abundant cobalt sulphide (CoS) is one of the potential and promising electrocatalysts which has been widely utilized in various energy storage/conversion devices such as Li-ion battery, supercapacitor [13][14][15] Kung et al. [17] carried out a two-step approach of chemical bath deposition (CBD) and sulfuration treatment to fabricate acicular CoS nanorod arrays. This new morphology and structure endowed the DSSCs based on CoS CE with a good efficiency. It is easily observed that the size and morphology of CoS have an important influence on electrochemical performance for I 3 − reduction, and carbon species have unique features and superiorities in increasing the conductivity of CoS CE materials, thus further improving its catalytic activities for I 3 − reduction. Carbon quantum dots (CQDs), nano-sized carbon particles, have attracted growing interest due to their high photochemical stability, low toxicity, good biocompatibility, and low environmental impact [18,19]. It has also been demonstrated that CQDs are of great potential in energy storage and conversions [20][21][22]. It is well known that there are abundant negative charged oxygen-containing functional groups on the surface of CQDs. These groups could further adsorb metal ions with positive charge easily to A BSTRACT Hybrid materials with alternate components and synergetic effects are promising and intriguing materials as electrodes for high-performance energy storage/conversion devices. Cobalt sulphide (CoS) is one of the low-cost but inactive catalysts as counter electrode (CE) for dye-sensitized solar cells (DSSCs). How to optimize its structure and further enhance its electrochemical activity for I3 − reduction remains a major challenge. Herein, a simple and efficient approach has been adopted to configure CoS sheets-coupled graphene quantum dots (GQDs) architectures via electrodepositing GQDs and CoS on the fl uorine doped tin oxide glass substrate. When employed as the binder-free CE for DSSCs, the as-made CoS-GQDs exhibits a high catalytic activity towards the reduction of I3 − , evidenced by the results of cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and Tafel polarization measurements. A conversion efficiency of 7.30% is achieved, being superior to CoS CE (5.55%) and Pt CE (6.94%) due to their synergetic effects. The present work provides a simple method for configuring low-cost binder-free CE materials for replacing Pt.