Quantum dots with emission in the spectral region from 525 to 535 nm are of special interest for their application in green LEDs and white-light generation, where CdSe/ZnS core-shell structured nanocrystals (NCs) are among promising candidates. In this study, triple-ligand system (trioctylphosphine oxide–oleic acid–oleylamine) was designed to improve the stability of CdSe NCs during the early reaction stage. With the precisely controlled reaction temperature (285 °C) and residence time (10 s) by the recently introduced microfluidic reaction technology, green luminescent CdSe NCs (λ = 522 nm) exhibiting narrow FWHM of PL (30 nm) was reproducibly obtained. After that, CdSe/ZnS core-shell NCs were achieved with efficient luminescence in the pure green spectral region, which demonstrated high PL QY up to 70% and narrow PL FWHM as 30 nm. The strengthened mass and heat transfer in the microchannel allowed the formation of highly luminescent CdSe/ZnS NCs under low reaction temperature and short residence time (T = 120 °C,t = 10 s). The successful formation of ZnS layer was evidence of the substantial improvement of PL intensity, being further confirmed by XRD, HRTEM, and EDS study.

Microreaction provides a controllable tool to synthesize CdSe nanocrystals (NCs) in an accelerated fashion. However, the surface traps created during the fast growth usually result in low photoluminescence (PL) efficiency for the formed products. Herein, the reproducible synthesis of highly luminescent CdSe NCs directly in open air was reported, with a microreactor as the controllable reaction tool. Spectra investigation elucidated that applying OLA both in Se and Cd stock solutions could advantageously promote the diffusion between the two precursors, resulting in narrow full-width-at-half maximum (FWHM) of PL (26 nm). Meanwhile, the addition of OLA in the source solution was demonstrated helpful to improve the reactivity of Cd monomer. In this case, the focus of size distribution was accomplished during the early reaction stage. Furthermore, if the volume percentage (vol.%) of OLA in the precursors exceeded a threshold of 37.5%, the resulted CdSe NCs demonstrated long-term fixing of size distribution up to 300 s. The observed phenomena facilitated the preparation of a size series of monodisperse CdSe NCs merely by the variation of residence time. With the volume percentage of OLA as 37.5% in the source solution, a 78 nm tuning of PL spectra (from 507 to 585) was obtained through the variation of residence time from 2 s to 160 s, while maintaining narrow FMWH of PL (26–31 nm) and high QY of PL (35–55%).

Herein, a room‐temperature liquid metal battery (LMB) with a solid lithium anode electrode and gallium–tin (Ga–Sn) alloy cathode electrode is reported. With the improved wettability of the electric collector and grain‐refined liquid metal droplets cathode, the aforementioned LMB exhibits good cyclic reversibility and negligible self‐discharge. The result shows that the assembled Li||Ga–Sn battery has a satisfactory specific capacity (409 mAh g−1) and high energy efficiency (up to 92%). The low melting point Ga–Sn alloy can construct fast kinetics for the redox reaction and improve the electrode reaction kinetics, imparting the Li||Ga–Sn system with high discharge voltage (0.77 V at 1C) and smaller polarization voltage at different current densities, which ensure the high Coulomb efficiency and good rate performance of the battery. Moreover, the battery stably cycles at 35 °C for 60 cycles at the 1C rate, with no significant capacity degradation. With good electrochemical performance, simple structure, easy maintenance, and high safety, this room‐temperature Li||Ga–Sn battery may be a promising choice for power grid energy storage applications.

No abstract

No abstract