Apr 25, 2024
9:45am - 10:00am
Room 347, Level 3, Summit
Tianshuo Zhao1,2,Qinghua Zhao2,Jaeyoung Lee2,Shengsong Yang2,Han Wang2,Ming-Yuan Chuang2,Yulian He3,Sarah Thompson2,Guannan Liu2,3,Nuri Oh2,Christopher Murray2,Cherie Kagan2
The University of Hong Kong1,University of Pennsylvania2,Yale University3
Tianshuo Zhao1,2,Qinghua Zhao2,Jaeyoung Lee2,Shengsong Yang2,Han Wang2,Ming-Yuan Chuang2,Yulian He3,Sarah Thompson2,Guannan Liu2,3,Nuri Oh2,Christopher Murray2,Cherie Kagan2
The University of Hong Kong1,University of Pennsylvania2,Yale University3
Colloidal InP quantum dots (QDs) have emerged as potential candidates for constructing nontoxic QD-based optoelectronic devices. However, charge transport in InP QD thin-film assemblies has been limitedly explored. Herein, we report the synthesis of ∼8 nm edge length (∼6.5 nm in height), tetrahedral InP QDs and study charge transport in thin films using the platform of the field-effect transistor (FET). We design a hybrid ligand-exchange strategy that combines solution-based exchange with S<sup>2–</sup> and solid-state exchange with N<sup>3–</sup> to enhance interdot coupling and control the n-doping of InP QD films. Further modifying the QD surface with thin, thermally evaporated Se overlayers yields FETs with an average electron mobility of 0.45 cm<sup>2</sup> V<sup>–1</sup> s<sup>–1</sup>, ∼10 times that of previously reported devices, and a higher on–off current ratio of 10<sup>3</sup>–10<sup>4</sup>. Analytical measurements suggest lower trap-state densities and longer carrier lifetimes in the Se-modified InP QD films, giving rise to a four-time longer carrier diffusion length.