光致发光
量子产额
铜
荧光
化学
光化学
纳米团簇
锌
发光
材料科学
纳米技术
光电子学
光学
物理
有机化学
作者
Neha Barnwal,Nilanjana Nandi,Priyanka Sarkar,Kalyanasis Sahu
标识
DOI:10.1002/asia.202400633
摘要
An assembly of metal nanoclusters driven by appropriate surface ligands and solvent environment may engender entirely new photoluminescence (PL). Herein, we first synthesize histidine (His) stabilized copper nanoparticles (CuNPs) and, subsequently, copper nanoclusters (CuNCs) from it using 3‐mercaptopropionic acid (MPA) as an etchant. The CuNCs originally emit bluish‐green (λem=470 nm) PL with a low quantum yield (QY∼1.8%). However, it transformed into a dual‐emissive nanocluster assembly (Zn‐CuNCs) in the presence of Zn(II) salt, having a distinct blue emission band (λem = 420 nm) and a red emission band (λem = 615 nm) with eight times QY (∼9.1%) enhancement. Adding dimethyl sulfoxide (DMSO) further modifies the emission intensities; the red band was amplified four times, while the blue band was diminished by 2.5 times. The transmission electron microscopy (TEM) images unveiled that the Zn‐CuNCs are a large assembly of tiny nanoclusters, which become more compact in DMSO. The blue emission possesses steady‐state fluorescence anisotropy, while the red emission shows no anisotropy. Further, near‐perfect white light emission(WLE) was rendered with CIE coordinates of (0.33, 0.32) by combining the dual emission of the Zn‐CuNCs with the original green emission of the CuNCs.
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