极性(国际关系)
材料科学
金属
光电子学
化学
冶金
生物化学
细胞
作者
Shuxin Chen,Zonglun Li,Shucong Li,Kunbo Xu,Ning Ma,Lei Yue,Xilian Jin,Ran Liu,Qingfeng Dong,Quanjun Li,Bingbing Liu
标识
DOI:10.1002/lpor.202500250
摘要
Abstract The burgeoning demand for efficient photoelectric devices has ignited a fervent exploration of strategies for regulating their performance. Herein, the enhancement and polarity switching in the photoresponse of MoS 2 photovoltaic devices with asymmetric electrodes are showcased by employing a pressure band engineering strategy. Specifically, the photoresponse of the Pt/MoS 2 /Ag setup escalates from 2 A W⁻¹ at 0.5 GPa to 4 A W⁻¹ at 2.3 GPa, showcasing a twofold enhancement, while displaying a successive decrease under higher pressure. Unforgettable is the fascinating and uncommon polarity switching behavior observed at 5.0 GPa in the Pt/MoS 2 /Au device, accompanied by a gradual decrease in photoresponse, implying its potential applications in logic gate devices. The dynamic evolution of photoresponse in Pt/MoS 2 /Ag and Pt/MoS 2 /Au devices can be ascribed to the variations in the bandgap, electron affinity, and work function of MoS 2 under high pressure, arising from the intensified interlayer interactions within MoS 2 . These findings validate the feasibility of enhancing photovoltaic device performance under pressure and unveil new avenues for exploring, manipulating, and comprehending high‐efficiency and multifunction photoelectric devices.
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