Two-Dimensional Silver(I)-Dithiocarboxylate Coordination Polymer Exhibiting Strong Near-Infrared Photothermal Effect.

ABSTRACT

Materials that demonstrate near-infrared (NIR) absorption and can simultaneously convert the electromagnetic irradiation into heat are promising for photothermal therapy. Traditionally, such a material is either pure inorganic, such as CuS, Ag2S, and carbon nanotube, or pure organic, such as polyaniline, polypyrrole, and conjugated polymers. Here we show that strong NIR photothermal effect can also be achieved in inorganic-organic hybrid coordination polymers (CPs) or metal-organic frameworks (MOFs). Our strategy is to construct CPs with inorganic Ag-S components that are interlinked by the organic ligands into a higher-dimensional hybrid network. Interestingly, the two resulting CPs, [Ag(Py-4-CSS)] n 1 and [Ag2(Py-4-CSS)(Py-4-CSSS)] n 2 (Py-4-CSS = pyridine-4-dithiocarboxylate; Py-4-CSSS = pyridine-4-perthiocarboxylate), show disparate structures due to the varied coordination mode of the pyridine group. For 1, the N atom coordinates to the Ag+ center and forms a two-dimensional square framework, while for 2, such a Ag-N bond is disconnected and forms only a one-dimensional structure. Interestingly, this difference leads to the distinct absorption properties in the NIR region. Under 800 nm radiation, the temperature of 1 can rise up to 24.5 °C in 3 min with photothermal conversion efficiency of 22.1%, which is about 2× that of pure inorganic Ag2S material and among the highest compared to various known inorganic materials, for example, Au nanoshells (13%), nanorods (21%), and Cu2- xSe nanocrystals (22%) irradiated with 800 nm light, while for 2, the NIR absorption is absent. This result first demonstrates that the inorganic-organic hybrid approach can be applied to construct superior NIR photothermal materials, but the control of the structure is vital. Here the coordinating nitrogen atoms in 1 are conceived to be critical in promoting the charge transfer between the dithiocarboxylate ligands. To elucidate the response to NIR irradiation of 1, we measured the heat capacity and dielectric constant of 1 and also performed density functional theory calculations. Significantly, the large dielectric constant and flat energy bands indicates 1 is much easier to be polarized and has a high electron effective mass. Thus, unlike the pure inorganic material, such as Ag2S, in which electron and hole can quantum mechanically combine to give off light, the joint-force of organic ligands in 1 effectively enhances polaronic recombination into heat.