The diverse functionalities of large N-heteroacenes continue to be developed in terms of their strategic synthesis and application in the organic electronic field. Here, we report a novel large stable pyrene-containing N-heteroacene with ten linearly-annulated rings in one row. Remarkably, it exhibited excellent tri-state resistive memory property, which held great promise to achieve ultrahigh-density data storage. To the best of our knowledge, it is the first demonstration of organic multistate memory device based on large N-heteroacene (n≥10), which provides guidelines for designing more proof-of-concept larger N-heteroacene-based memory electronics
We found novel organic charge-transfer salts that exhibit reversible resistive memory switching phen...
In this work, two metallopolymers (P1 and P2) were designed and synthesized through coupling of ferr...
Although organic multilevel resistance memories have attracted much attention for potential realizat...
To achieve ultrahigh density memory devices with the capacity of 3n or larger, organic materials wit...
N-substituted heteroacenes have been widely used as electroactive layers in organic electronic devic...
N-heteroacenes with the CH groups in the backbone of acenes replaced by N atoms are expected to own ...
The uniformity of operating parameters in organic nonvolatile memory devices is very important to av...
A novel thiadiazoloquinoxaline (TQ)-based donor–acceptor (D–A)-type N-heteroacene (<b>Py-1-TQ</b>) h...
Organic π-conjugated materials have attracted much attention in recent years because these materials...
The possibility of developing fully organic electronic circuits is critically dependent on the abili...
A chargeable layer is an essential element for charge transfer and trapping in a transistor-based no...
\u3cp\u3eOrganic molecules and semiconductors have been proposed as active part of a large variety o...
International audienceAn organic ambipolar charge trapping non-volatile memory device is proposed ba...
Three donor–acceptor and twisted anthraquinone azo molecules were synthesized, and the effects of co...
Acenes, usually defined as segments of “graphene”, consist of linearly annulated benzene rings, and ...
We found novel organic charge-transfer salts that exhibit reversible resistive memory switching phen...
In this work, two metallopolymers (P1 and P2) were designed and synthesized through coupling of ferr...
Although organic multilevel resistance memories have attracted much attention for potential realizat...
To achieve ultrahigh density memory devices with the capacity of 3n or larger, organic materials wit...
N-substituted heteroacenes have been widely used as electroactive layers in organic electronic devic...
N-heteroacenes with the CH groups in the backbone of acenes replaced by N atoms are expected to own ...
The uniformity of operating parameters in organic nonvolatile memory devices is very important to av...
A novel thiadiazoloquinoxaline (TQ)-based donor–acceptor (D–A)-type N-heteroacene (<b>Py-1-TQ</b>) h...
Organic π-conjugated materials have attracted much attention in recent years because these materials...
The possibility of developing fully organic electronic circuits is critically dependent on the abili...
A chargeable layer is an essential element for charge transfer and trapping in a transistor-based no...
\u3cp\u3eOrganic molecules and semiconductors have been proposed as active part of a large variety o...
International audienceAn organic ambipolar charge trapping non-volatile memory device is proposed ba...
Three donor–acceptor and twisted anthraquinone azo molecules were synthesized, and the effects of co...
Acenes, usually defined as segments of “graphene”, consist of linearly annulated benzene rings, and ...
We found novel organic charge-transfer salts that exhibit reversible resistive memory switching phen...
In this work, two metallopolymers (P1 and P2) were designed and synthesized through coupling of ferr...
Although organic multilevel resistance memories have attracted much attention for potential realizat...