Tracking Cation Exchange in Individual Nanowires via Transistor Characterization.

Cation exchange is a versatile method for modifying the material composition and properties of nanostructures. However, control of the degree of exchange and material properties is difficult at the single-particle level. Successive cation exchange from CdSe to Ag2Se has been utilized here on the same individual nanowires to monitor the change of electronic properties in field-effect transistor devices. The transistors were fabricated by direct synthesis of CdSe nanowires on prepatterned substrates followed by optical lithography. The devices were then subjected to cation exchange by submerging them in an exchange solution containing silver nitrate. By removal of the devices from solution and probing the electrical transport properties at different times, the change in electronic properties of individual nanowires could be monitored throughout the entire exchange reaction from CdSe to Ag2Se. Transistor characterization revealed that the electrical conductivity can be tuned by up to 8 orders of magnitude and the charge-carrier mobility by 7 orders of magnitude. While analysis of the material composition by energy dispersive X-ray spectroscopy confirmed successful cation exchange from CdSe to Ag2Se, X-ray fluorescence spectroscopy proved that cation exchange also took place below the contacts. The method presented here demonstrates an efficient way to tune the material composition and access the resulting properties nondestructively at the single-particle level. This approach can be readily applied to many other material systems and can be used to study the electrical properties of nanostructures as a function of material composition or to optimize nanostructure-based devices after fabrication.

Photodegradation of CuBi2 O4 Films Evidenced by Fast Formation of Metallic Bi using Operando Surface-sensitive X-ray Scattering.

CuBi2 O4 has recently emerged as a promising photocathode for photo-electrochemical (PEC) water splitting. However, its fast degradation under operation currently poses a limit to its application. Here, we report a novel method to study operando the semiconductor-electrolyte interface during PEC operation by surface-sensitive high-energy X-ray scattering. We find that a fast decrease in the generated photocurrents correlates directly with the formation of a metallic Bi phase. We further show that the slower formation of metallic Cu, as well as the dissolution of the electrode in contact with the electrolyte, further affect the CuBi2 O4 activity and morphology. Our study provides a comprehensive picture of the degradation mechanisms affecting CuBi2 O4 electrodes under operation and poses the methodological basis to investigate the photocorrosion processes affecting a wide range of PEC materials.

Two-Dimensional Superstructures from the Gas Phase: Directed Assembly of Copper-Sulfide Nanoplatelets.

We report on a novel plasma-assisted approach for the deposition of free-standing two-dimensional superstructures via directed assembly of copper-sulfide nanoplatelets in the gas phase. For this, the copper-organic complex bis-[bis(N,N-diethyldithiocarbamato)-copper(II)] is thermally evaporated and transported into a capacitively coupled rf plasma to form two-dimensional nanoplatelets upon fragmentation. On a substrate, the highly anisotropic platelets are attached in a directed edge-to-edge configuration. We found that a high substrate temperature of 400 °C is necessary for the 2D vertical growth of copper sulfide. Using plasma reinforces the directional assembly and leads to nanowalls which are several micrometers high with the thickness of a single nanoplatelet. The morphology and crystallographic composition of the emerging superstructures were extensively investigated via scanning and transmission electron microscopy as well as electron diffraction. The data reveal the (010) plane to be the preferred axis for the arrangement of the nanoplatelets.