Synthesis of large CZTSe nanoparticles through a two-step hot-injection method

Grain boundaries in Cu2ZnSn(SxSe1x)4 (CZTSSe) thin films act as a defect that reduces the mobility of the charges. Hence one way to improve the performance of these thin film solar cells is to increase the grain size in the films. Most of the synthesis methods published so far for CZTSSe colloidal nanoparticles can achieve a general size distribution range from 5–20 nm. This is where the particle size will saturate for most recipes used today. The assumption is that uniform size distribution is good for grain growth in a thin film but based on packing considerations, an optimal mixture of large and small nanoparticles that can easily be dispersed in non-polar solvents could be better. Cu2ZnSnS4 (CZTS) and Cu2ZnSnSe4 (CZTSe) nanoparticles are synthesized using the hot-injection method with oleylamine, trioctylphosphine, and hexadecane as the solvents. Selenium (Se) is introduced in the liquid phase to encourage grain growth – liquid selenization. This eliminates the need to anneal the film in a Secontaining atmosphere and allows for a more environmentally friendly process with lower temperatures and shorter annealing times. We show that a good dispersion can be achieved by choosing suitable surfactant molecules, solvents and precursors, and by controlling the initial monomer concentration. Additionally, we show how our new synthesis route can be utilized to achieve targeted ratios of CZTS and CZTSe nanoparticles to be used for mixed-phase CZTSSe thin films

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Picosecond dynamics of internal exciton transitions in CdSe nanorods

The picosecond dynamics of excitons in colloidal CdSe nanorods are directly measured via their 1s to 2p-like internal transitions by ultra-broadband terahertz spectroscopy. Broadened absorption peaks from both the longitudinal and transverse states are observed at 8.5 and 11 THz, respectively. The onset of exciton-LO phonon coupling appears as a bleach in the optical conductivity spectra at the LO phonon energy for times > 1 ps after excitation. Simulations show a suppressed exciton temperature due to thermally excited hole states being rapidly captured onto ligands or unpassivated surface states. The relaxation kinetics are manipulated and the longitudinal transition is quenched by surface ligand exchange with hole capturing pyridine

Influences of graphene oxide support on the electrochemical performances of graphene oxide-MnO2 nanocomposites

MnO2 supported on graphene oxide (GO) made from different graphite materials has been synthesized and further investigated as electrode materials for supercapacitors. The structure and morphology of MnO2-GO nanocomposites are characterized by X-ray diffraction, X-ray photoemission spectroscopy, scanning electron microscopy, transmission electron microscopy, Raman spectroscopy, and Nitrogen adsorption-desorption. As demonstrated, the GO fabricated from commercial expanded graphite (denoted as GO(1)) possesses more functional groups and larger interplane gap compared to the GO from commercial graphite powder (denoted as GO(2)). The surface area and functionalities of GO have significant effects on the morphology and electrochemical activity of MnO2, which lead to the fact that the loading amount of MnO2 on GO(1) is much higher than that on GO(2). Elemental analysis performed via inductively coupled plasma optical emission spectroscopy confirmed higher amounts of MnO2 loading on GO(1). As the electrode of supercapacitor, MnO2-GO(1) nanocomposites show larger capacitance (307.7 F g-1) and better electrochemical activity than MnO2-GO(2) possibly due to the high loading, good uniformity, and homogeneous distribution of MnO2 on GO(1) support

Ultrafast Spin-To-Charge Conversion at the Surface of Topological Insulator Thin Films

Strong spin-orbit coupling, resulting in the formation of spin-momentum-locked surface states, endows topological insulators with superior spin-to-charge conversion characteristics, though the dynamics that govern it have remained elusive. Here, we present an all-optical method that enables unprecedented tracking of the ultrafast dynamics of spin-to-charge conversion in a prototypical topological insulator Bi$_2$Se$_3$/ferromagnetic Co heterostructure, down to the sub-picosecond timescale. Compared to pure Bi$_2$Se$_3$ or Co, we observe a giant terahertz emission in the heterostructure than originates from spin-to-charge conversion, in which the topological surface states play a crucial role. We identify a 0.12-picosecond timescale that sets a technological speed limit of spin-to-charge conversion processes in topological insulators. In addition, we show that the spin-to-charge conversion efficiency is temperature independent in Bi$_2$Se$_3$ as expected from the nature of the surface states, paving the way for designing next-generation high-speed opto-spintronic devices based on topological insulators at room temperature.Comment: 19 pages, 4 figure