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中国物理学会期刊

纳米成核点辅助结晶对钙钛矿光电探测器性能的影响

CSTR: 32037.14.aps.71.20220189

Effect of nano-nucleation sites assisted crystallization on performance of perovskite photodetector

CSTR: 32037.14.aps.71.20220189
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  • 有机无机杂化钙钛矿材料因具有可调节的带隙宽度、优异的载流子传输性能、可低温溶液法制备等优点, 近年来在光电器件的应用研究上受到了广泛的关注. 对于平面光电导型探测器, 电荷在两电极之间需横穿钙钛矿层, 由于钙钛矿晶体的形成能较低, 在晶界和薄膜表面易产生缺陷, 光生载流子被缺陷阻挡而加剧激子的非辐射复合, 造成器件光电性能下降. 本文通过在钙钛矿界面层下方引入微量的氧化石墨烯纳米片作为钙钛矿晶体的有效成核点, 使得钙钛矿晶体可依附于氧化石墨烯形核, 降低钙钛矿晶体成核势垒的同时与钙钛矿形成铅-氧键, 最终获得晶体颗粒增大、晶界数量减少、薄膜致密的钙钛矿层. 由于氧化石墨烯在玻璃基底上的含量极低, 大片玻璃基底裸露并与钙钛矿直接接触, 因此钙钛矿层应视为制备在玻璃基底上. 在氧化石墨烯纳米片的影响下钙钛矿与玻璃基底的接触更为紧密, 有效降低界面间的激子非辐射复合概率, 提高了界面间电荷传输性能. 最终, 在氧化石墨烯纳米片最优制备参数的影响下, 钙钛矿光电探测器光电流相比空白对照器件提高了1个数量级, 在3 V偏压下的开关电流比为5.22 × 103, 并且最优的光电探测器的光响应速度明显提高, 上升时间为9.6 ms, 下降时间为6.6 ms.

     

    Photodetector occupies an important position in the sensor family, but most of the photoelectric conversion materials of photodetectors are inorganic semiconductors, such as GaAs, GaN, Ge and Si, these inorganic semiconductors are usually prepared by complicated methods and high cost, and furthermore, they have poor mechanical flexibility. Organic-inorganic hybrid perovskite materials serving as visible-light sensitizers have the advantages of balanced electron and hole mobilities, adjustable bandgaps, high absorption coefficients, low temperature solution preparation, which make the materials a suitable candidate for inorganic semiconductors.
    For planar photodetectors, carriers have greater probabilities to be trapped by the defects in the perovskite films, therefore it is important to fabricate a high-quality perovskite film. However, owing to the low formation energy of perovskite crystals, defects prove to occur on the film surface and grain boundaries, which aggravate the performance of perovskite optoelectronic devices. In this work, we introduce a small quantity of graphene oxide nanosheets (GOSs) on bare glass substrate as effective nucleation sites of perovskite crystals. Owing to the extremely low density of GOSs and large exposed glass basement, the GOSs cannot be regarded as an interface layer. The existence of GOSs on smooth substance reduces the perovskite nucleation barrier, leading to a more preferential crystal growth in these locations, and binds tightly with glass substrate, which passivates the defects efficiently. Meanwhile, the element of O in the GOSs can create Pb–O bond with Pb in the CH3NH3PbI3, further improving the crystal of perovskite. On this basis, planner perovskite photodetector with a structure of glass/GOSs/CH3NH3PbI3/MoO3/Au is fabricated. By adjusting the concentration of GOSs deionized water dispersion under the same spin-coating condition, the photoelectric conversion performance of perovskite photodetector is enhanced. Under the influence of the optimal concentration of GOSs, photocurrent of the champion photodetector (1.15 × 10–6 A) is an order of magnitude higher than that of reference device without GOSs modified (3.58 × 10–7 A) at 3 V bias, leading to a high ON/OFF current ratio of 5.22 × 103. Besides, improved photoresponse speed is also found in the champion device, with a rise time of 9.6 ms and a decay time of 6.6 ms, respectively. The enhanced performance of GOSs modified perovskite photodetector can be attributed to the significantly reduced defects bringing about an enhanced charge separation and collection performance in the CH3NH3PbI3 films.
    By introducing extremely low quantity GOSs as the effective perovskite crystal nucleation sites, the perovskite crystallization and thin film can be effectively improved, leading to a positive effect on the performance of perovskite photodetector. This method has a certain universality, and therefore it has a reference value for other structures of perovskite photoelectric devices.

     

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