P-N junctions exist in many solid-state organic devices, such as light-emitting diodes, solar cells, thermoelectric devices, etc. Creating p-n junctions by bulk chemical doping in a single organic material (like… Click to show full abstract
P-N junctions exist in many solid-state organic devices, such as light-emitting diodes, solar cells, thermoelectric devices, etc. Creating p-n junctions by bulk chemical doping in a single organic material (like silicon doped by boron and phosphorus) may capitalize the vast scientific and technological groundwork established in the inorganic semiconducting field. However, high performance single organic material p-n junctions have been seldom reported because the diffusion of the dopant counter ions often leads to transient rectification properties. Herein, we report a new type of lateral fully organic diodes created in single donor-acceptor (D-A) copolymer films with only one p-type dopant. The achieved lateral devices exhibited high current densities of ∼3.83 A/cm2 and a high rectification ratio of ∼2100, which are beyond the requirements for high frequency identification tags. The p- to n-type polarity switching mechanism was proposed after spectroscopic and structural tests. Decent stability of the organic diode was obtained which was due to the long channel length and low diffusion speed of the large size of dopants. This work opens the opportunities to create p-n junctions in ways of silicon based inorganic semiconductors and promises new opportunities for integrating organic materials for flexible and printable organic devices. This article is protected by copyright. All rights reserved.
               
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