김영훈 교수

Energy-harvesting devices such as piezoelectric and triboelectric nanogenerators (NGs), which can convert mechanical energy into electricity, are under development to be combined with various electronics. In particular, the rapid progress in microscale electronics such as nanorobotics or microelectromechanical devices has strongly increased the demand for ultrathin film devices. Therefore, the thickness, highly uniform structure, chemical composition, interfacial adhesion/interactions, and elect

Lead-free, water-resistant photovoltaic absorbers are of significant interest for use in environment-friendly and water-stable thin film solar cells. However, there are no reports on the water-resistance characteristics of such photoactive materials. Here, we demonstrate that silver bismuth sulfide (AgBiS2) nanocrystal solids exhibit inherent water resistance and can be employed as effective photovoltaic absorbers in all-solid-state thin film solar cells that show outstanding air and moisture st

AgBiS2 nanocrystals (NCs) have emerged as attractive absorbers in eco-friendly photovoltaics because of their nontoxic components and high absorption coefficient. Native long-chain ligands of AgBiS2 NCs should be replaced with short-chain ligands for their photovoltaics; however, conventional approaches have been performed using solid-state ligand exchange (SSLE), resulting in inhomogeneous NC aggregation, broad bandtail, large trap density, and resultantly low open-circuit voltage (VOC) in devi

A crack-free, mesoporous silica thin film (see Figure) has been formed on a macroporous support by prefilling the support pores with poly(vinyl alcohol). The ordered mesoporous silica thin film with narrow pore size distribution was synthesized via a sol–gel route. These thin films have a number of potential applications, including in membrane-based separation processes, as catalysts, and as chemical sensors.

Bandtail broadening originating from increasing the polydispersity of colloidal quantum dots (CQDs) deteriorates open-circuit voltage (VOC) and hinders charge-carrier transport in CQD photovoltaics. The development of colloidal synthetic routes has enabled preparing monodisperse perovskite CQDs (Pe-CQDs) that have attracted attention as promising absorbers in CQD photovoltaics. However, polar-antisolvent-based purification induces the dissolution and agglomeration of Pe-CQDs, resulting in an irr

Advances in surface chemistry and manipulation of CsPbI3 perovskite quantum dots (PQDs) have enabled the replacement of native long-chain ligands with short-chain ligands, leading to their photovoltaic applications; however, there are no reports on those of wide-bandgap and green-emitting CsPbBr3 PQDs that are promising in high-voltage and colorful building-integrated photovoltaics. Binding energies required for ligand adsorption/desorption alter according to halide compositions of PQDs because

CsPbI₃ perovskite quantum dots (CsPbI₃-PQDs) have recently come into focus as a light-harvesting material that can act as a platform through which to combine the material advantages of both perovskites and QDs. However, the low cubic-phase stability of CsPbI₃-PQDs in ambient conditions has been recognized as a factor that inhibits device stability. TiO₂ nanoparticles are the most regularly used materials as an electron transport layer (ETL) in CsPbI<su

Colloidal quantum dots (CQDs) are considered as next-generation semiconductors owing to their tunable optical and electrical properties depending on their particle size and shape. The characteristics of CQDs are mainly governed by their surface chemistry, and the ligand exchange process plays a crucial role in determining their surface states. Worldwide studies toward the realization of high-quality quantum dots have led to advances in ligand exchange methods, and these procedures are usually ca

Composites comprising copper-doped zinc sulfide phosphor microparticles embedded in polydimethylsiloxane (ZnS:Cu-PDMS) have received significant attention over the past decade because of their bright and durable mechanoluminescence (ML); however, the underlying mechanism of this unique ML remains unclear. This study reports empirical and theoretical findings that confirm this ML is an electroluminescence (EL) of the ZnS:Cu phosphor induced by the triboelectricity generated at the ZnS:Cu micropar

Abstract Perovskite quantum dots (PQDs) have been considered promising and effective photovoltaic absorber due to their superior optoelectronic properties and inherent material merits combining perovskites and QDs. However, they exhibit low moisture stability at room humidity (20–30%) owing to many surface defect sites generated by inefficient ligand exchange process. These surface traps must be re-passivated to improve both charge transport ability and moisture stability. To address this issue,

Ternary silver bismuth sulfide (AgBiS2) colloidal nanocrystals (NCs) have been recognized as a photovoltaic absorber for environmentally-friendly and low-temperature-processed thin film solar cells. However, previous synthetic methods involving hot injection of sulfur precursors into metal oleate precursor solutions do not provide a balance between nucleation and growth, leading to AgBiS2 NCs with broad size distributions. Here, we demonstrate the modified synthetic route that size distribution

Abstract The electron transport layer (ETL) is a critical component in perovskite quantum dot (PQD) solar cells, significantly impacting their photovoltaic performance and stability. Low-temperature ETL deposition methods are especially desirable for fabricating flexible solar cells on polymer substrates. Herein, we propose a room-temperature-processed tin oxide (SnO 2 ) ETL preparation method for flexible PQD solar cells. The process involves synthesizing highly crystalline SnO 2 nanocrystals s