<p>The instability of halide perovskites under working conditions or during complex postprocessing is challenging for practical applications. Here we developed a room-temperature, two-phase assembling strategy to synthesize single-unit-cell perovskite chains within single-walled carbon nanotubes (SWCNTs). This approach is efficient, scalable and tailorable, and can be used to assemble a range of single-chain perovskites. The single-unit-cell-chain perovskites show unconventional stoichiometries (such as [Cs<sub>4</sub>PbI<sub>5</sub>]<sup>+</sup>) due to dimensionality reduction and are balanced by negatively charged nanotubes. A direct X-ray detector constructed with high-entropy-Cs<sub>3</sub>MCl<sub>6</sub>@SWCNT exhibits outstanding performance, with a high sensitivity of <InlineEquation ID="IEq1"> <InlineMediaObject> <ImageObject Color="BlackWhite" FileRef="44160_2025_785_Article_IEq1.gif" Format="GIF" Height="21" Rendition="HTML" Resolution="72" Type="Linedraw" Width="176" /> </InlineMediaObject> <EquationSource Format="TEX">\(1.22\times10^{4}\,\upmu{\mathrm{C}}\,{\mathrm{Gy}}_{\mathrm{air}}^{-1}\,{\mathrm{cm}}^{-2}\)</EquationSource> <EquationSource Format="MATHML"><math> <mrow> <mn>1.22</mn> <mo>×</mo> <mn>1</mn> <msup> <mrow> <mn>0</mn> </mrow> <mrow> <mn>4</mn> </mrow> </msup> <mspace width="0.25em" /> <mi mathvariant="normal">μ</mi> <mi mathvariant="normal">C</mi> <mspace width="0.25em" /> <msubsup> <mrow> <mi mathvariant="normal">Gy</mi> </mrow> <mrow> <mi mathvariant="normal">air</mi> </mrow> <mrow> <mo>−</mo> <mn>1</mn> </mrow> </msubsup> <mspace width="0.25em" /> <msup> <mrow> <mi mathvariant="normal">cm</mi> </mrow> <mrow> <mo>−</mo> <mn>2</mn> </mrow> </msup> </mrow> </math></EquationSource> </InlineEquation>, a low dark current density of 0.2 nA cm<sup>−2</sup>, a negligible dark current drift of 8.5 × 10<sup>−7</sup> nA cm<sup>−1</sup> s<sup>−1</sup> V<sup>−1</sup> and a superior detection limit of 16.6 nGy<sub>air</sub> s<sup>−1</sup>. These surpass various common semiconductor and state-of-the-art perovskite detectors due to the ionic character of perovskite@SWCNT inducing a strong cation–<i>π</i> interaction, suppressing ion migration. The device is stable under harsh conditions, including continuous X-ray irradiation, high temperatures, exposure to ambient air for 91 days and immersion for 96 h in water. This low-cost synthetic methodology paves the way for the commercialization of potential perovskite X-ray detectors for medical and industrial applications.</p><p></p>

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Synthesis of single-unit-cell-thick perovskites by liquid-phase confined assembly for high-performance ultrastable X-ray detectors

  • Meihui Song,
  • Bo Zhao,
  • Bowen Li,
  • Kun Wang,
  • Yulong Jiang,
  • Guodong Jia,
  • Xin Zhao,
  • Boyuan Yu,
  • Yunlong Li,
  • Feng Yang

摘要

The instability of halide perovskites under working conditions or during complex postprocessing is challenging for practical applications. Here we developed a room-temperature, two-phase assembling strategy to synthesize single-unit-cell perovskite chains within single-walled carbon nanotubes (SWCNTs). This approach is efficient, scalable and tailorable, and can be used to assemble a range of single-chain perovskites. The single-unit-cell-chain perovskites show unconventional stoichiometries (such as [Cs4PbI5]+) due to dimensionality reduction and are balanced by negatively charged nanotubes. A direct X-ray detector constructed with high-entropy-Cs3MCl6@SWCNT exhibits outstanding performance, with a high sensitivity of \(1.22\times10^{4}\,\upmu{\mathrm{C}}\,{\mathrm{Gy}}_{\mathrm{air}}^{-1}\,{\mathrm{cm}}^{-2}\) 1.22 × 1 0 4 μ C Gy air 1 cm 2 , a low dark current density of 0.2 nA cm−2, a negligible dark current drift of 8.5 × 10−7 nA cm−1 s−1 V−1 and a superior detection limit of 16.6 nGyair s−1. These surpass various common semiconductor and state-of-the-art perovskite detectors due to the ionic character of perovskite@SWCNT inducing a strong cation–π interaction, suppressing ion migration. The device is stable under harsh conditions, including continuous X-ray irradiation, high temperatures, exposure to ambient air for 91 days and immersion for 96 h in water. This low-cost synthetic methodology paves the way for the commercialization of potential perovskite X-ray detectors for medical and industrial applications.