A multilayered p-type photoabsorber based on kesterite Cu₂ZnSnSe₄ has been functionalized with inexpensive and easily scalable amorphous MoS₂ electrocatalyst by cathodic photoelectrodeposition. The resulting photocathodes with a final composition of Mo/MoSe₂/Cu₂ZnSnSe₄/CdS/ZnO/ITO/MoS₂ (where ITO = indium tin oxide) feature one of the highest hydrogen evolution catalytic current density reported to date at a potential E = 0 V vs RHE (-18 mA/cm² in pH 2) under 1 sun illumination. A comparison of the performance of the photoelectrode with an analogous dark electrode with composition ITO/MoS₂ allows us to estimate a photovoltage of 430 mV, which is very close to the working voltage of an equivalent photovoltaic cell with open circuit voltage V_OC = 464 mV. The photoelectrodes show sustained activity at -10 mA/cm² above the thermodynamic potential of the H⁺/H₂ redox couple (E = +86 mV) for 1 hour without any loss of activity. Prolonged reaction times up to 4 hours show no degradation of the photoabsorber multilayered architecture but a decrease in the thickness of the the MoS₂ electrocatalytic film due to the mechanical stress caused by the hydrogen bubbles forming on the surface of the electrode. The MoS₂ layer is key not only to catalyze the catalytic reaction but also to protect the photoabsorber from the corrosive electrolyte solution. The adhesion of the MoS₂ electrocatalytic film on the ITO top layer is critical for the stability during hydrogen evolution catalysis.