Abstract:Photo-switchable
organic field-effect transistors (OFETs) represent
an important platform for designing memory devices for a diverse array
of products including security (brand-protection, copy-protection,
keyless entry, etc.), credit cards, tickets, and multiple wearable
organic electronics applications. Herein, we present a new concept
by introducing self-assembled monolayers of donor–acceptor
porphyrin–fullerene dyads as light-responsive triggers modulating
the electrical characteristics of OFETs and thus p… Show more
“…The technique has been extensively used in the study of silicon materials, for example, photovoltaic devices, and has been suggested as a potential scheme to readout coherent spin states of quantum bits in the semiconductor-based quantum computer concept. [211] The OFET approach discussed above [205] is here extended to qubit measurements with separation between the qubit states and the charge carriers, allowing retention of the spin coherence properties of molecular qubits. One challenge for implementing this readout scheme is the OFET detection of the electric dipole field of the CT state instead of the full charge of a memory element.…”
Section: Field-effect Transistormentioning
confidence: 99%
“…Along this line, very recent work has demonstrated that monolayers of D/A porphyrin–fullerene dyads can act as light‐responsive triggers modulating the electrical characteristics of OFETs ( Figure a). [ 205 ] The operational mechanism of these devices has been described as follows. After the absorption of photons by D, photoinduced ET from D to A occurs, thereby generating a CS state.…”
Section: From Sketches To Real Systemsmentioning
confidence: 99%
“…a) Layout fabricated and characterized in ref. [205] based on porphyrin–fullerene dyads anchored to AlOx through carboxylic groups. b) Exemplary OFET device proposed for the spin‐to‐charge conversion based on CISS effect.…”
Molecular spins are promising building blocks of future quantum technologies thanks to the unparalleled flexibility provided by chemistry, which allows the design of complex structures targeted for specific applications. However, their weak interaction with external stimuli makes it difficult to access their state at the single‐molecule level, a fundamental tool for their use, for example, in quantum computing and sensing. Here, an innovative solution exploiting the interplay between chirality and magnetism using the chirality‐induced spin selectivity effect on electron transfer processes is foreseen. It is envisioned to use a spin‐to‐charge conversion mechanism that can be realized by connecting a molecular spin qubit to a dyad where an electron donor and an electron acceptor are linked by a chiral bridge. By numerical simulations based on realistic parameters, it is shown that the chirality‐induced spin selectivity effect could enable initialization, manipulation, and single‐spin readout of molecular qubits and qudits even at relatively high temperatures.
“…The technique has been extensively used in the study of silicon materials, for example, photovoltaic devices, and has been suggested as a potential scheme to readout coherent spin states of quantum bits in the semiconductor-based quantum computer concept. [211] The OFET approach discussed above [205] is here extended to qubit measurements with separation between the qubit states and the charge carriers, allowing retention of the spin coherence properties of molecular qubits. One challenge for implementing this readout scheme is the OFET detection of the electric dipole field of the CT state instead of the full charge of a memory element.…”
Section: Field-effect Transistormentioning
confidence: 99%
“…Along this line, very recent work has demonstrated that monolayers of D/A porphyrin–fullerene dyads can act as light‐responsive triggers modulating the electrical characteristics of OFETs ( Figure a). [ 205 ] The operational mechanism of these devices has been described as follows. After the absorption of photons by D, photoinduced ET from D to A occurs, thereby generating a CS state.…”
Section: From Sketches To Real Systemsmentioning
confidence: 99%
“…a) Layout fabricated and characterized in ref. [205] based on porphyrin–fullerene dyads anchored to AlOx through carboxylic groups. b) Exemplary OFET device proposed for the spin‐to‐charge conversion based on CISS effect.…”
Molecular spins are promising building blocks of future quantum technologies thanks to the unparalleled flexibility provided by chemistry, which allows the design of complex structures targeted for specific applications. However, their weak interaction with external stimuli makes it difficult to access their state at the single‐molecule level, a fundamental tool for their use, for example, in quantum computing and sensing. Here, an innovative solution exploiting the interplay between chirality and magnetism using the chirality‐induced spin selectivity effect on electron transfer processes is foreseen. It is envisioned to use a spin‐to‐charge conversion mechanism that can be realized by connecting a molecular spin qubit to a dyad where an electron donor and an electron acceptor are linked by a chiral bridge. By numerical simulations based on realistic parameters, it is shown that the chirality‐induced spin selectivity effect could enable initialization, manipulation, and single‐spin readout of molecular qubits and qudits even at relatively high temperatures.
“…49,50 More recently, we demonstrated that light-induced isomerization is not needed at all and self-assembled monolayers of the porphyrin-fullerene dyads could enable efficient electrooptical switching of OFETs. 51 While donor-acceptor dyads are known to be highly photoactive, their molecular structures are usually sophisticated and the synthesis is challenging. Therefore, a promising research direction to simplify the structure of the memory OFETs and make their components less expensive would be using some simple organic dyes as receptor components at the semiconductor/dielectric interface instead of donor-acceptor dyads or photochromic molecules.…”
New BODIPY-coumarin dye was synthesized, characterized, and utilized as a light-sensitive component in optically programmed OFET-based memory cells and photodetectors. The designed photoswitchable OFETs assembled with both n-type (fullerene C60)...
“…Precise control over the alignment of functional materials is highly desirable in a broad variety of applications including sensors, biomedical electronics, and energy and data storage. − Extensive research studies have focused on the photosensitive materials combined with their nanoscale self-assembly in new optoelectronics. − Utilizing the versatility and compatibility, prototypes of electronic devices based on a field-effect transistor (FET) architecture were generally reported. − Recently, of increasing interest is the phototransistor memory featuring an additional electret for storing and processing optical signals over long-distance transmission with wide bandwidth, high-density data storage, low-power consumption, as well as orthogonal operation in optical/electrical. Therefore, phototransistor memory is regarded to play a pivotal role in exploring next-generation optical communication systems and artificial intelligence. − To date, various materials such as nanocomposites, organic–inorganic hybrid perovskites, transition metal dichalcogenides, and liquid-crystalline materials , have been developed for the functional assembly of phototransistors.…”
With
the explosive growth in data generation, phototransistor memory
capable of multibit data storage with higher stability and switchability
is highly desired to enhance the capacity of storage media. An innovative
intrinsic dual-functional block copolymer (BCP)-based electret consisting
of poly(ethylene oxide)-block-poly(1-pyrenemethyl
methacrylate) (PEO-b-PPyMA) was used to elucidate
the effect of the BCP design and self-assembled morphology on phototransistor
memory. Regarding the constituent polymers in the BCP, PPyMA serves
as the photogate, while PEO enhances the charge stability through
electrostatic interaction. On the other hand, the solvent-annealed
BCP film, representing well-defined hexagonal cylinders, shows an
excellent charge trapping/stabilizing capability. Accordingly, the
phototransistor memory, with PEO-b-PPyMA as an electret,
produced a wide memory window (54 V), a superior memory stability
(>106), and a fast photoresponsive characteristic. This
research presents for the first time a new concept on the intrinsic
dual-functional BCP to produce high-performance nonvolatile memory
and demonstrates the potential of this approach for prospective application
in optoelectronic devices.
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