光电化学电池
二氧化钛
氧化锡
无机化学
光催化
化学工程
光电化学
电极
电解质
半导体
化学
分解水
作者
Xiaodong Li,Zemin Zhang,Lulu Chen,Zhongping Liu,Jianli Cheng,Wei Ni,Erqing Xie,Bin Wang
标识
DOI:10.1016/j.jpowsour.2014.07.060
摘要
Abstract CdS quantum dots (QDs)-sensitized branched TiO 2 /SnO 2 heterojunction (B–SnO 2 NF–CdS) with suitable combination of band gap and band alignment constitutes a promising architecture for photoanode for H 2 generation. This novel structure combines the conflicting advantageous features of slow interfacial electron recombination, long electron life time, fast electron transport and visible light absorption. Remarkable photocurrent density of 3.40 mA cm −2 at zero bias (vs. standard calomel electrode) has been obtained in a three electrode configuration, more than two times as large as that of TiO 2 –CdS photoanode. The B–SnO 2 NF–CdS yields a high maximum applied bias photon-to-current efficiency (ABPE) of 2.18% at an applied bias of ∼0.316 V vs. reversible hydrogen electrode (RHE), indicating excellent hydrogen generation performance at low bias. Moreover, on the basis of experimental results, we ascribe the remarkable “dark current/voltage” to the effect of primary cell. The influence of the primary cell on PEC hydrogen production is discussed.
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