化学
二亚胺
全色胶片
均苯四甲酸二酐
吸收(声学)
光热治疗
光化学
接受者
分子
纳米技术
苝
图层(电子)
光学
有机化学
物理
凝聚态物理
材料科学
图像分辨率
聚酰亚胺
作者
Silang Chen,Hao Zeng,Ci Kong,Feixiang Cheng,Jian‐Jun Liu
标识
DOI:10.1021/acs.inorgchem.5c04002
摘要
The incorporation of donor-acceptor components into metal-organic frameworks (MOFs) is an effective approach for developing efficient near-infrared (NIR) photothermal conversion materials; yet, their precise structural design and synthetic methodologies still present significant challenges. In this work, we present a distinctive MOF material Zn2(bpPDI)(TTFTB)·solvent (MOF 1) constructed by the coordinated assembly of donor-acceptor components, featuring a tetrathiafulvalene tetrabenzoate (TTFTB) electron donor and a bis-pyridyl-substituted pyromellitic diimide (bpPDI) electron acceptor. The material demonstrates significant intrinsic intermolecular electron-transfer capability and possesses a long-lived TTFTB•+ radical cation and a bpPDI•- radical anion. These characteristics enable panchromatic absorption spanning the visible to the second near-infrared (NIR-II) region, thus allowing efficient NIR photothermal conversion. Under NIR light irradiation, MOF 1 achieves efficient photothermal conversion (ΔTmax = 137 °C under 0.5 W cm-2 laser exposure), including rare NIR-II photothermal conversion capabilities, while exhibiting excellent thermal stability and cycling durability.
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