钝化
悬空债券
材料科学
光电流
载流子
析氧
分解水
化学工程
催化作用
光催化
异质结
表面状态
纳米技术
图层(电子)
载流子寿命
阳极
降级(电信)
化学物理
氧化还原
能量转换效率
无定形固体
纳米晶材料
光化学
光电子学
表面工程
硒化铜铟镓太阳电池
表面能
作者
Ziqian Chen,Baoxin Ge,Feiya Shu,Yuntao Hu,Jie Zeng,Biyi Chen
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2026-03-03
卷期号:16 (6): 5979-5992
被引量:4
标识
DOI:10.1021/acscatal.6c00210
摘要
Surface passivation is critical for mitigating detrimental surface states in photoelectrodes, yet the unsatisfactory charge transfer efficiency at the semiconductor-passivation layer interface severely limits the achievable current density. Constructing atomic-scale charge transfer channels to ensure efficient carrier extraction while preserving passivation is a Frontier in photoelectrode design but remains challenging. Here, an ultrathin (∼2 nm), conformal, amorphous iron–nickel–phytate complex (PA–FeNi) layer was engineered on an Fe 2 O 3 surface via interfacial coordination assembly, establishing Fe–O–P bond linkages to optimize interfacial carrier transport. The atomic-level integration saturated the surface dangling bonds on Fe 2 O 3 to mitigate recombination losses and created efficient charge-transfer pathways, promoting photogenerated hole migration to the PA–FeNi layer. Furthermore, the PA–FeNi layer as the oxygen evolution reaction (OER) cocatalyst significantly reduced the energy barrier of the rate-determining *OH → *O step. These synergistic effects extend the average lifetime of photogenerated holes from 1.5 to 297.7 ps, a value far exceeding those reported previously for photocatalytic and photoelectrochemical systems. As expected, the optimized Fe 2 O 3 @PA–FeNi photoanode delivers a notable photocurrent density of 3.29 mA cm –2 at 1.23 V RHE, exhibiting a 3.05-fold enhancement over pristine Fe 2 O 3, while maintaining 99.8% of its initial performance after 24 h durability test. Importantly, the PA–metal complex strategy demonstrates universal applicability, substantially improving the performances of BiVO 4, TiO 2, and WO 3 photoanodes through the dual optimization of interfacial charge transfer and OER kinetics. This work proposes a facile, versatile, and cost-efficient interfacial engineering paradigm for designing an ideal photoelectrode/cocatalyst interface that synergistically regulates charge kinetics and catalytic activity in solar energy conversion systems.
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