I agree with the answers above. Both techniques are possible: CV and EIS. In the case of CV, you have to measure the current in a place where there is only capacitive current. Then, this current is v.C (scan rate multiplied by the capacity) and you can extract the capacity. You have to record the CV in a solution without electroactive species (without faradaic contribution to the current)
Both methods are applicable. With one addition: it is necessary to know mass of active electrode and fraction of the substance whose electrochemical capacity you want to determine. That is, you need to weigh the components before slurry preparing, as well as the electrode (minus substrate). The resulting capaty value should be divided by the mass of the active substance [mA*hrs/g].