Search

Luminescent metal-organic frameworks (LMOFs) are promising materials for organic light-emitting diode (OLED) alternatives to silicate-based LEDs due to their tuneable structure and programmability. Yet, the 3D nature of LMOFs creates challenges for stability, optical transparency, and device integration. Metal-organic nanosheets (MONs) potentially overcome these limitations by combining the benefits of MOFs with an atomically thin morphology of large planar dimensions. Here, we report the bottom-up synthesis of atomically thin ZIF-7-III MONs via facile low-energy salt-templating. Employing guest@MOF design, the fluorophores Rhodamine B and Fluorescein were intercalated into ZIF-7 nanosheets (Z7-NS) to form light emissive systems exhibiting intense and highly photostable fluorescence. Aggregation and F\"orster resonance energy transfer, enabled by the MON framework, were revealed as the mechanisms behind fluorescence. By varying guest concentration, these mechanisms provided predictable quantified control over emission chromaticity of a dual-guest Z7-NS material and the definition of an 'emission chromaticity fingerprint' - a unique subset of the visible spectrum which a material can emit by fluorescence., Comment: 27 Pages, 7 Figures, Supplementary Information

Organic photoswitchable molecules have struggled in solid state form to fulfill their remarkable potential, in terms of photoswitching performance and long-term stability when compared to their inorganic counterparts. We report the concept of non-electron deficient host's surface with optimal porosity and hydrophobicity, as a priori strategy to design photoefficient organic solid-state photochromic materials with outstanding mechanical robustness. When exposed to a light stimulus including natural sunlight, the photoswitchable nanocomposite changes color promptly and reversibly, in a matter of seconds along with excellent photo-fatigue resistance, which are on a par with inorganic photochromes. Exemplars of commercially viable prototypes that are optically clear, comprising smart windows, complex photochromic sculptures, and self-erasing rewritable devices, were engineered by direct blending with resilient polymers; particularly, the use of high-stiffness polymer (> 2 GPa) is no longer an insurmountable challenge. Finally, photochromic films with anticounterfeiting features could be manufactured through precision inkjet printing of nanocrystals., Comment: 12 pages, 5 figures, Supplementary Information

Ultra-sensitive and highly selective iodine gas sensors play a crucial role during the nuclear radiation leak for a timely detection and mitigation of pollution, ensuring the safety of a vast number of operators and subsequent integrity of the facility. Herein, we rationally designed a metal-organic framework (MOF) that exhibits an outstanding performance with an almost billion-fold enhancement in the electrical response due to its optimized hydrophobicity, which allows the easy migration of iodine molecules though the channels and the presence of suitable interaction sites, temporarily anchoring the target molecule for ultra-trace sensing. The prototype sensor tested in demanding environments demonstrates its high selectivity, ultra-trace parts per billion (ppb)-level sensitivity, good reversibility, and a very fast response time even at high frequencies compared to existing adsorbents, including commercially available materials. Further, the iodine sensing at the atomic level was studied in detail by measuring the electrical response of a single crystal and, the optimal thickness of the MOF layer was identified for an industrially-viable prototype sensor by using inkjet printing. In a wider perspective, we propose a general strategy towards electrically efficient sensing materials with hybrid functionalities for engineering high-sensitivity iodine sensors for a safe and sustainable future., Comment: 14 Pages, 5 Figures, 1 Supporting Information (32 pages)

Mechanofluorochromic materials are of great significance for the fabrication of innovative sensors and optoelectronics. However, efficient mechanofluorochromic materials are rarely explored due to the deficiency of existing design strategies. Here, we demonstrate the incarceration of aggregation-induced emission (AIE) materials within metal-organic framework (MOF) single crystals to construct a composite system with turn-on mechanofluorochromism. A new type of AIE@MOF material was designed: integrating a zeolitic MOF (ZIF-71) and tetraphenylethylene (TPE, a topical AIE material) to generate a TPE@ZIF-71 system with exceptional turn-on type mechanofluorochromism. Using terahertz vibrational spectroscopy, we show the unique fluorochromism emanates from the enhanced nanoconfinement effect exerted by ZIF-71 host on TPE guest under pressure and its permanent fluorescence after stress release. Compared with pure TPE, we demonstrate the nanoconfinement in AIE@MOF not only changes the TPE's turn-off type sensing behavior to a turn-on type, but boosts the original sensitivity markedly by tenfold. Significantly, because ZIF-71 prevents the spontaneous recrystallization of TPE upon unloading, this allows TPE@ZIF-71 to record the stress history. This is the first demonstration of the Guest@MOF system combining the concepts of AIE and MOF; its promising properties and potential engineering applications will stimulate new directions pertaining to luminescent stress sensors and smart optics., Comment: 21 pages, 4 figures, 1 scheme