Nanocrystal Precursor Incorporating Separated Reaction Mechanisms for Nucleation and Growth to Unleash the Potential of Heat-Up Synthesis.
Nanocrystal Precursor Incorporating Separated Reaction Mechanisms for Nucleation and Growth to Unleash the Potential of Heat-Up Synthesis.
复制标题
纳米晶体前驱体结合了成核和生长的分离反应机制,释放了加热合成的潜力。
作者:
Joonhyuck Park;A. Jayaraman;Xudong Wang;J. Zhao;Hee
A heat-up method for quantum dots (QDs) synthesis holds distinctive benefits for large-scale production with its simplicity, scalability, and high reproducibility. Its applications, however, have been limited because it inevitably yields a strong overlap between the nucleation and growth stages. We addressed this long-standing problem by introducing a precursor having separated reaction paths for nucleation and growth. Unlike existing precursors, which employs a shared intermediate for both reactions, 9-mercapto-9-borabicyclo[3.3.1]nonane (BBN-SH) induces growth via surface-assisted conversion and drives nucleation via cluster formation in solution. Furthermore, this precursor chemistry embeds an efficient mechanism to suppress nucleation during growth. As such, BBN-SH allows heat-up-based growth of high-quality shells that are comparable to those created by the injection method. It is also notable that BBN-SH-based heat-up synthesis shows mitigated sensitivity to temperature fluctuation; therefore, it is highly suitable for industrial-scale reactions. We established a simple, scalable, and economic scheme for core/shell QDs by streamlining quantitative core synthesis and heat-up-based shell growth and showed that the scheme produces QDs of comparable quality to those produced by the traditional method. Here, we introduce a precursor that drives a distinctive mode of nanoparticle growth. We anticipate our study to inspire the design of other precursors and unleash the full potential of heat-up synthesis.
影响因子:
15
作者:
Han HS;Devaraj NK;Lee J;Hilderbrand SA;Weissleder R;Bawendi MG
通讯作者:
Bawendi MG
影响因子:
41.2
作者:
Chen O;Zhao J;Chauhan VP;Cui J;Wong C;Harris DK;Wei H;Han HS;Fukumura D;Jain RK;Bawendi MG
通讯作者:
Bawendi MG