自然键轨道
热电性
极化(电化学)
电场
密度泛函理论
载流子
分解水
材料科学
兴奋剂
光电子学
重组
凝聚态物理
化学物理
化学
光催化
物理
计算化学
物理化学
铁电性
电介质
基因
催化作用
量子力学
生物化学
作者
Tianhao Li,Mengnan Ruan,Zhengang Guo,Chengyi Wang,Zhifeng Liu
标识
DOI:10.1002/chem.202301967
摘要
Abstract Pyroelectric materials in the field of photoelectrochemical (PEC) water splitting still face the problems of difficult low spontaneous polarization intensity and excessive carrier recombination. Based on the above problems, we altered the interaction between S−Nb−S in the [NbO] 6−x ‐xS structure, and the constructed [NbO] 6−x ‐xS structure achieved the regulation of charge density change and spontaneous polarization. The results show that under the stimulation of light and temperature fluctuations, the current density of the NS‐4 photoanode is as high as 0.574 mA/cm 2 at 1.23 V RHE , which is about 1.59 times higher than the pure NaNbO 3 current density value, and the NS −4 photoanode achieves IPCE value of 16.08 %. The first‐principles density‐functional theory calculations (DFT) reveal the principle of the [NbO] 6−x ‐xS structure for the suppression function of the carrier recombination and the improvement function of the pyroelectric effect. The analysis shows that the S‐doping leads to the weakening of S−Nb−S interactions in the [NbO] 6−x ‐xS structure, which improves the pyroelectric effect and suppresses the photo/pyro‐generated carrier recombination, and effectively enhances the performance of the pyro‐photo‐electric synergistic water splitting system. This work promotes the development of pyroelectric materials in the field of photoelectrochemical water splitting.
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