铁电性
异质结
极化(电化学)
分子动力学
范德瓦尔斯力
载流子
材料科学
密度泛函理论
量子效率
载流子寿命
激发态
化学物理
量子阱
光催化
光电子学
物理
化学
物理化学
计算化学
光学
原子物理学
分子
电介质
硅
催化作用
有机化学
激光器
生物化学
作者
Xingxing Jiang,Jieyao Tan,Dongyu Liu,Yexin Feng,Ke‐Qiu Chen,Run Long,Andrey S. Vasenko
标识
DOI:10.1021/acs.jpclett.4c00404
摘要
The rapid recombination of photogenerated carriers heavily restricts the photocatalytic efficiency. Here, we propose a new strategy to improve catalytic efficiency based on the ferroelectric van der Waals heterostructure (CuBiP2Se6/C2N). Combining density functional theory and the nonadiabatic molecular dynamics (NAMD) method, we have systematically analyzed the ground-state properties and carrier dynamics images in the CuBiP2Se6/C2N heterostructure. Our calculations showed that the ferroelectric polarization of CuBiP2Se6 provides the internal driving force for the photogenerated carriers separation. NAMD results demonstrate that the excited-state carrier transfer and recombination processes in the CuBiP2Se6/C2N are consistent with a type II mechanism. Meanwhile, constructing the ferroelectric heterostructure can effectively prolong the carrier lifetime, from ∼65.98 to ∼124.54 ps. Moreover, the high quantum efficiency and tunable band edge positions mean that the CuBiP2Se6/C2N heterostructure is an excellent potential candidate material for photocatalytic water splitting.
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