光电阴极
分解水
材料科学
异质结
工作职能
光电子学
表面光电压
串联
纳米技术
制氢
氧化还原
载流子
能量转换效率
费米能级
化学工程
光催化
瓶颈
电子
光电化学电池
光催化分解水
工作(物理)
光电化学
氢
电荷(物理)
科技与社会
耗尽区
析氧
有效核电荷
纳米材料
作者
Q. Li,D.S. Zhang,Wenchao Jiang,Jiajun Wang,Haibo Chi,RenGui Li,W. Y. Yu,Fengtao Fan,Chunmei Ding,Can Li
标识
DOI:10.1002/aenm.202504315
摘要
ABSTRACT Hydrogen production via photoelectrocatalytic (PEC) water splitting is a promising way, but great challenges remain in promoting charge separation and transfer, which has been a long‐standing bottleneck in PEC systems. Herein, we construct a BiVO 4 ‐based photoanode via successively introducing Fe 2 TiO 4 , NiOOH, GO, and Co‐complex cocatalyst, achieving an applied bias photon‐to‐current efficiency of 2.4%. Importantly, we found that Fe 2 TiO 4 featured with Fe 2+/3+ and Ti 3+/4+ redox states, eliminates the Fermi level pinning of BiVO 4 and may function as a dual‐redox electron mediator, which enhances charge separation and transfer. By in situ potential measurements, it is found that the interface layers can shift the hole quasi‐Fermi level positively and electron quasi‐Fermi level negatively, increasing the photovoltage and intrinsic driving force for PEC reaction. A tandem device composed of the BiVO 4 ‐based photoanode and a bulk heterojunction photocathode delivers a solar‐to‐hydrogen efficiency of as high as 4.7%. This work identifies Fe 2 TiO 4 as an efficient dual‐redox mediator, which promotes PEC water splitting via regulating the quasi‐Fermi levels of photoanodes.
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