摘要
We prepared antimony metal films via electrodeposition, followed by the synthesis of Sb2S3films through a chemical vapor phase reaction. Finally, an Sb2O3film was deposited onto the Sb2S3film using a chemical bath method, successfully constructing a heterojunction photocathode of Sb2S3/Sb2O3; the synthesized Sb2S3/Sb2O3heterojunction is classified as a Type I heterostructure. The resulting Sb2S3/Sb2O3heterojunction exhibited a photocurrent density of −0.056 mA cm−2at −0.15 V (vs. RHE), which is 1.40 times higher than that of Sb2S3alone under simulated solar illumination. Additionally, the Sb2S3/Sb2O3heterojunction demonstrated a lower carrier recombination rate and a faster charge transfer rate compared to Sb2S3, as evidenced by photoluminescence and electrochemical impedance spectroscopy tests. For these reasons, the Sb2S3/Sb2O3heterojunction obtained a hydrogen precipitation rate of 0.163mL cm−2h−1, which is twice the hydrogen precipitation rate of Sb2S3, under the condition of 60 min of light exposure. The significant enhancement in photoelectrochemical performance is attributed to the formation of the Sb2S3/Sb2O3heterojunction, which improves both carrier separation and charge transfer efficiency. This heterojunction strategy holds promising potential for visible light-driven photoelectrochemical water splitting.
危险品化学品经营许可证(带存储)