This study investigates the feasibility of using a mixed phase manganese dioxide (MnO 2 ) in the graphite supported Pt catalyst layer to perform a light-driven photoelectrochemical cell. The effects of the conditions of preparing a mixed phase MnO 2 on their properties are evaluated. By adjusting the precursor concentrations down to 0.1 M, the multi-diffraction peaks of α−, β−, ε− and γ−MnO 2 can be obtained and shown to display strong vibrational bands related to the pyrolusite and ramsdellite structure. In particular, a significant enhancement on the photodegradation test has been observed with an optimum degradation efficiency ratio (monomeric/dimeric) of 1.089. Furthermore, by adding a mixed phase MnO 2 in the catalyst layer, the electrode shows the related hydrophilic surface characteristics, and the advancing contact angle, receding contact angle and contact angle decrease to 121.91 • , 117.77 • and 106.64 • , respectively. After light illumination, a significant light-induced hydrogen generation by CH 3 OH aqueous solution splitting is observed. The incorporation of mixed phase MnO 2 within graphite supported Pt catalyst layer largely enhances the photoelectrochemical cell performance from 2.18 mW cm −2 to 2.92 mW cm −2 . The use of solar-induced photocatalytic reactions to conduct water splitting to produce hydrogen is currently one of the world's most important alternative energy technologies being developed. In addition to reducing mankind's demand for fossil fuels, the hydrogen energy can also convert solar energy into another form of energy and be stored. According to the literature, the photocatalytic water-splitting reaction system can be divided into tri-electrodes and bi-electrodes; 1 the three-pole electrode system consists of a semiconductor photoanode, platinum counter electrode and reference electrode. The process of the photocatalytic reaction must be subject to an additional bias voltage for it to be carried out. However, the electron-transfer kinetics and cell/electrolyte resistance limit the efficiency of H 2 generation in such cells. In contrast, the membrane electrode assembly as the main structure of the bi-electrodes photoelectrochemical cell could be started without additional bias. It needs only the light to be irradiated on the photoelectrode end, taking advantage of the semiconductor materials on the photoelectrode surface to absorb the photon energy and, thus, stimulate the electron-hole pairs, so the water-splitting reaction could be started. 2-5 Nevertheless, when energy level of the H 2 /H 2 O redox reaction is higher than the Fermi-energy of the cathode electrode, an applied bias is still necessary for a two electrode configuration cell. 6 The key to producing hydrogen from photocatalytic water-splitting lies in the photocatalytic material. The energy of the electron-holes that are generated through the photocatalytic material being stimulated must be identical to the electric potential of the oxidation-reduction reaction. Only then can the oxidation-reduction reaction start t...