期刊
JOURNAL OF MATERIALS CHEMISTRY C
卷 11, 期 43, 页码 15197-15204出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/d3tc03244b
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In this study, a strategy for constructing Ga2O3/BFMO heterojunction-based photodetectors was proposed to enhance responsivity and detectivity by utilizing the built-in electric field and ferroelectric depolarization electric field for carrier separation. The fabricated photodetector exhibited tunable performance under zero bias, with higher performance observed in the upward poling state and under weak light illumination.
Ga2O3-based photovoltaic-type (i.e., self-driven) deep ultraviolet (DUV) photodetectors have attracted extensive attention due to their broad application prospects in civilian and military fields. However, their common drawback of poor light sensitivity (i.e., responsivity and detectivity) has greatly hindered their practical applications. In this work, we propose a strategy for constructing a Ga2O3/BiFe0.95Mn0.05O3 (BFMO) ferroelectric/semiconductor heterojunction-based photodetector with higher responsivity and detectivity than single BFMO and single Ga2O3 devices by exploiting the built-in electric field at the Ga2O3/BFMO heterojunction interface (EGa2O3/BFMO) and the ferroelectric depolarization electric field across the BFMO (Edp) to promote the separation of photogenerated carriers. The fabricated Ga2O3/BFMO heterojunction photodetector exhibits tunable performance under zero bias. Higher responsivity (19.01 mA W-1 @ 260 nm) and detectivity (4.52 x 1011 Jones @ 260 nm) are observed for the photodetector in the upward poling state than that in the unpoled state, which can be attributed to the coupling effect of Edp and EGa2O3/BFMO. Moreover, the photodetector shows even higher responsivity (23.54 mA W-1) and detectivity (5.58 x 1011 Jones) under weak light illumination (P260nm = 0.002 mW cm-2), with values much higher than those reported for Ga2O3-based heterojunction photodetectors. This work offers an effective approach for boosting the performance of self-driven UV photodetectors.
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