Deng Yalei, Chen Xufeng, Liang Jing, Wang Yuanyuan
State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing, China.
Front Chem. 2022 Apr 12;10:860781. doi: 10.3389/fchem.2022.860781. eCollection 2022.
Stabilizing nanocrystals (NCs) with high fluorescence quantum efficiency in suitable solvents and tuning of their optical properties precisely are critical for designing and assembling optoelectrical devices. Here, we demonstrated that by replacing the original X-type ligand (R-COO) with triethylborate (TEB), zinc-blend structure nanoplatelets (Zb-NPLs) turn from hydrophobic to hydrophilic and are quite stable in polar solvents. More importantly, a large shift of 253 meV is observed for the TEB-passivated NPLs, which can be attributed to the strain of the crystal lattice and the electron or hole delocalizing into the ligand shell. It is worth noting that unlike conventional inorganic ligands, such as metal chalcogenide complexes or halides that quench fluorescence, TEB-treated NPLs maintain 100% of their original brightness in polar solvents with a slight increase in full width at half maximum (FWHM, 32 nm). Furthermore, we explored the possibility of employing TEB as surface ligands for NPLs with different thicknesses and compositions. We believe the discovery of new surface chemistry using borate-related ligands can greatly expand the potential application areas of NPLs.
在合适的溶剂中稳定具有高荧光量子效率的纳米晶体(NCs)并精确调节其光学性质对于光电器件的设计和组装至关重要。在此,我们证明通过用硼酸三乙酯(TEB)取代原始的X型配体(R-COO),闪锌矿结构纳米片(Zb-NPLs)从疏水性转变为亲水性,并且在极性溶剂中相当稳定。更重要的是,对于TEB钝化的NPLs观察到253 meV的大位移,这可归因于晶格应变以及电子或空穴离域到配体壳层中。值得注意的是,与传统的无机配体不同,例如会淬灭荧光的金属硫族化物配合物或卤化物,TEB处理的NPLs在极性溶剂中保持其原始亮度的100%,半高宽(FWHM,32 nm)略有增加。此外,我们探索了将TEB用作不同厚度和组成的NPLs的表面配体的可能性。我们相信使用硼酸盐相关配体发现新的表面化学可以极大地扩展NPLs的潜在应用领域。