Proton exchange membrane fuel cells(PEMFCs)suffer extreme CO poisoning even at PPM level(<10 ppm),owning to the preferential CO adsorption and the consequential blockage of the catalyst sur-face.Herein,however,we report that CO itself can become an easily convertible fuel in PEMFC using atomically dispersed Rh catalysts(Rh-N-C).With CO to CO2 conversion initiates at 0 V,pure CO powered fuel cell attains unprecedented power density at 236 mW cm-2,with maximum CO turnover frequency(64.65 s-1,363 K)far exceeding any chemical or electrochemical catalysts reported.Moreover,this fea-ture enables efficient CO selective removal from H2 gas stream through the PEMFC technique,with CO concentration reduced by one order of magnitude through running only one single cell,while simultane-ously harvesting electricity.We attribute such catalytic behavior to the weak CO adsorption and the co-activation of H2O due to the interplay between two adjacent Rh sites.