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Published on: August 23, 2012
Structural Reconfiguration via Alternating Cation Intercalation of Chiral Hybrid Perovskites for Efficient
Guirong Chen1, Zeng-Kui Zhu1, Jianbo Wu2,3
1College of Chemistry and Materials, Key Laboratory of Fluorine and Silicon for Energy Materials and Chemistry of Ministry of Education, Jiangxi Normal University, Nanchang, Jiangxi 330022, P. R. China.
Abstract:
2D hybrid perovskites (HPs) have great potential for high-performance X-ray detection due to their strong radiation absorption and flexible structure. However, there remains a need to explore avenues for enhancing their detection capabilities. Optimizing the detection performance through modification of their structural properties presents a promising strategy. Herein, we explore the impact of modifying the organic spacer layer in two distinct 2D layered HPs, namely, Ruddlesden-Popper (R-MPA)2PbBr4 (R-1, R-MPA = methylphenethylammonium) and (R-MPA)EAPbBr4 (EA = ethylammonium) (R-2) with alternating cation intercalation (ACI), on their X-ray detection performance. The insertion of EA into R-2 results in a flatter inorganic skeleton, narrower spacing, and higher density compared to R-1. This structural modification effectively optimizes carrier transport and X-ray absorption in R-2, enhancing the X-ray detection performance. Notably, R-2 exhibits a polar structure with intrinsic spontaneous polarization, contributing to a bulk photovoltaic of 0.4 V. This feature enables R-2 single-crystal detectors to achieve self-driven X-ray detection with a low detection limit of 82.5 nGy s-1 under a 0 V bias. This work highlights the efficacy of the ACI strategy in structural modification and its significant effect on X-ray detection properties, providing insights for the design and optimization of new materials.

