Construction of Multifunctional and Adjustable Langmuir–Blodgett Composite Films Containing Black Phosphorus with High Stability for Optically Electrical Applications
Abstract:Fabrication of composite thin-film materials based on black phosphorus (BP) will greatly broaden the applications of BP in various areas. However, it is still a challenge to prepare a BP-based composite film with good stability and controllable structure. In this work, a series of BP-based composite Langmuir−Blodgett (LB) films are prepared by the selfassembly of polyethyleneimine (PEI)-modified BP nanosheets (BPNSs) (BPNS-PEI) and dye molecules. The presence of PEI greatly improves the stability of BPNSs. As … Show more
“…The mechanism of the acid–alkali response is shown in Figure g. The interface structure and charge transfer of the LB films can be affected by heteroatoms in the subphase (like nitrogen atoms) and the molecular structure of the films . For the carbazole molecules/MO LB films, influenced by the external acid–alkali gases atmosphere, we speculate that the acidic sulfonic acid and the alkali dimethylamino in the MO form a conjugated system of p -aminoquinone structure, which changes the internal structure of the composite films and affects the charge transfer .…”
Section: Resultsmentioning
confidence: 91%
“…The interface structure and charge transfer of the LB films can be affected by heteroatoms in the subphase (like nitrogen atoms) and the molecular structure of the films. 25 For the carbazole molecules/MO LB films, influenced by the external acid− alkali gases atmosphere, we speculate that the acidic sulfonic acid and the alkali dimethylamino in the MO form a conjugated system of p-aminoquinone structure, which changes the internal structure of the composite films and affects the charge transfer. 26 For the other two composite films, the color change of the films may be attributed to the protonation and deprotonation of the N−H and −NH 2 groups in the dye molecules.…”
The complex and variable environments
are challenging the development
of related detection and analysis. Ammonia (NH3) and hydrogen
chloride (HCl) gases are both commonly used in industry, but they
are considered to be toxic and corrosive substances that can threaten
human health and the environment. Therefore, it is necessary here
to develop a convenient, sensitive, and reliable sensor device for
acid–alkali gas detection. Herein, we propose the synthesis
strategy of an ultrathin film gas sensor based on the pH-responsive,
self-powered, and visible composite Langmuir–Blodgett (LB)
films. In our work, the LB films with nanometric thicknesses are obtained
based on the sensitive materials of two novel carbazole structural
sensitizers (abbreviated as CS-35 and CS-37) and several dye molecules.
The composite LB films are formed with Carbazole samples and dye molecules
through hydrogen bonding, π–π stacking, synergistic
electrostatic interactions, and hydrophobic interactions, existing
as J-aggregate or H-aggregate. The formation of high-quality and uniform
Langmuir films is confirmed with transmission electron microscope
(TEM), UV–vis spectrum, atomic force microscopy (AFM), and
other measurements. In addition, based on the simple protonation and
deprotonation, the prepared LB films can be assembled into a visual
sensor for the response of pH gases. The response is confirmed by
the study of ultraviolet spectroscopy and electrical output in vertical
contact separation mode, which potentially unlocks a sustainable future
for the application of ultrathin self-powered gas sensors.
“…The mechanism of the acid–alkali response is shown in Figure g. The interface structure and charge transfer of the LB films can be affected by heteroatoms in the subphase (like nitrogen atoms) and the molecular structure of the films . For the carbazole molecules/MO LB films, influenced by the external acid–alkali gases atmosphere, we speculate that the acidic sulfonic acid and the alkali dimethylamino in the MO form a conjugated system of p -aminoquinone structure, which changes the internal structure of the composite films and affects the charge transfer .…”
Section: Resultsmentioning
confidence: 91%
“…The interface structure and charge transfer of the LB films can be affected by heteroatoms in the subphase (like nitrogen atoms) and the molecular structure of the films. 25 For the carbazole molecules/MO LB films, influenced by the external acid− alkali gases atmosphere, we speculate that the acidic sulfonic acid and the alkali dimethylamino in the MO form a conjugated system of p-aminoquinone structure, which changes the internal structure of the composite films and affects the charge transfer. 26 For the other two composite films, the color change of the films may be attributed to the protonation and deprotonation of the N−H and −NH 2 groups in the dye molecules.…”
The complex and variable environments
are challenging the development
of related detection and analysis. Ammonia (NH3) and hydrogen
chloride (HCl) gases are both commonly used in industry, but they
are considered to be toxic and corrosive substances that can threaten
human health and the environment. Therefore, it is necessary here
to develop a convenient, sensitive, and reliable sensor device for
acid–alkali gas detection. Herein, we propose the synthesis
strategy of an ultrathin film gas sensor based on the pH-responsive,
self-powered, and visible composite Langmuir–Blodgett (LB)
films. In our work, the LB films with nanometric thicknesses are obtained
based on the sensitive materials of two novel carbazole structural
sensitizers (abbreviated as CS-35 and CS-37) and several dye molecules.
The composite LB films are formed with Carbazole samples and dye molecules
through hydrogen bonding, π–π stacking, synergistic
electrostatic interactions, and hydrophobic interactions, existing
as J-aggregate or H-aggregate. The formation of high-quality and uniform
Langmuir films is confirmed with transmission electron microscope
(TEM), UV–vis spectrum, atomic force microscopy (AFM), and
other measurements. In addition, based on the simple protonation and
deprotonation, the prepared LB films can be assembled into a visual
sensor for the response of pH gases. The response is confirmed by
the study of ultraviolet spectroscopy and electrical output in vertical
contact separation mode, which potentially unlocks a sustainable future
for the application of ultrathin self-powered gas sensors.
“…S3†), and distinct signal peaks appeared at positions 359.8, 435.1, and 463.3 cm −1 of the spectrum, corresponding to the Raman shifts caused by the A 1 g , B 2g , and A 2 g lattice vibrations of BP, respectively. 25,26,30,31 Strong diffraction peaks at 17.1°, 34.3°, and 52.4° are seen in the XRD image in Fig. 2g, representing the (020), (040), and (060) crystal planes of BP, respectively.…”
Section: Resultsmentioning
confidence: 99%
“…21 The reported thermal conductivities of monolayer BP along the zigzag crystallographic direction, armchair direction, and through-plane are about 101, 36, and 5.5 W m −1 K −1 , respectively, as assessed by the time-resolved magneto-optical Kerr effect. 22 At present, BP is mainly used in photoelectric functional devices, 23,24 photosensitive thin films, 25 and other research fields, while research on BP-containing fillers as thermal management materials has rarely been conducted. Therefore, it is interesting and meaningful to investigate the potential of BP as a filler to enhance the thermal transport performance of thermal management materials.…”
Heat dissipation of portable electronics is in great demand of lightweight and flexible films with superior thermal transport properties. Despite extensive efforts, enhancing the intrinsic low thermal conductivity of polymers...
“…The result implies that BMIC-BO-4Cl exhibits higher charge separation efficiency of photogenerated electron-hole pairs. [17] Next, the charge transfer properties of the two materials were characterized by electronic conductivity via the electrochemical impedance spectroscopy (EIS) technique (Figure 2f). The charge transfer resistance can be read out from the semicircle's diameter of the Nyquist plot.…”
NIR-II-emitting photosensitizers (PSs) have attracted great research interest due to their promising clinical applications in imaging-guided photodynamic therapy (PDT). However, it is still challenging to realize highly efficient PDT on NIR-II PSs. In this work, we develop a chlorination-mediated π-π organizing strategy to improve the PDT of a PS with conjugation-extended A-D-A architecture. The significant dipole moment of the carbon-chlorine bond and the strong intermolecular interactions of chlorine atoms bring on compact π-π stacking in the chlorine-substituted PS, which facilitates energy/charge transfer and promotes the photochemical reactions of PDT. Consequently, the resultant NIR-II emitting PS exhibits a leading PDT performance with a yield of reactive oxygen species higher than that of previously reported long-wavelength PSs. These findings will enlighten the future design of NIR-II emitting PSs with enhanced PDT efficiency.
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