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Although hybrid solar cells take advantages of both inorganic and organic semiconductors for high performance, there have not been comparably photoelectric conversion efficiencies as expected from this kind of solar cells till now. The photoelectric response behavior of inorganic/organic hybrid solar cells has been explained on the theory of inorganic solar cells, but the distinctive wavelength dependent photoelectric character of organic semiconductors has not been well considered. In this work, Ag 2 S/organic bulk heterojunction solar cell devices were designed and fabricated in-situ on indium tin oxide (ITO) based on the direct metal surface elemental reaction (DMSER) method, to understand the corresponding photoinduced charge carrier dynamics under different wavelength light. The commonly used small molecule Spiro-OMeTAD and polymeric PTB7-Th were selected as the organic components of the fabricated solar cells. In Ag 2 S/Spiro-OMeTAD, Ag 2 S donated the charge carriers and controlled the photoinduced charge carrier dynamics of the devices at both 355 nm and 532 nm lights. Under 532 nm light, the PTB7-Th acted as hole transport materials (HTM) rather than charge carrier donor. These results indicated that hybrid thin films without wavelength dependent charge carrier dynamics is preferred for high performance solar cells. [ABSTRACT FROM AUTHOR]