Conformationally Constrained Bidentate Ligands Drive Record-High NIR Quantum Yield in Cu Nanoclusters
Atom-precise copper nanoclusters (Cu NCs) with near-infrared (NIR) luminescence show promise in biomedical and optoelectronic applications, due to their cost-effectiveness, low toxicity, and tunable photophysics. However, their practical application is limited by extremely low NIR photoluminescence quantum yields (PLQYs) (<1%) at room-temperature (RT) in solution, as well as their pronounced sensitivity to oxidation. Here we present two structurally well-defined 15-nuclear Cu NCs, the monophosphine-stabilized copper-thiolate cluster [Cu<sub>15</sub>(TPP)<sub>6</sub>(PET)<sub>13</sub>]<sup>2+</sup> (<b>Cu</b><sub><b>15</b></sub><b>-TPP</b>) and its diphosphine analogue [Cu<sub>15</sub>(DPPB)<sub>3</sub>(PET)<sub>12</sub>H]<sup>2+</sup> (<b>Cu</b><sub><b>15</b></sub><b>-DPPB</b>), which exhibit drastically different NIR PLQYs. Single-crystal X-ray diffraction (SC-XRD) reveals that both NCs feature a comparable triple-helical Cu<sub>9</sub> core but distinct surface ligand arrangements. In <b>Cu</b><sub><b>15</b></sub><b>-DPPB</b>, the diphosphine chelator DPPB adopts a <i>cis-cis</i> conformation to rigidify ligand shell. In contrast, the monodentate TPP ligand in <b>Cu</b><sub><b>15</b></sub><b>-TPP</b> leads to a less rigidified ligand shell. This structural disparity enables a 186-fold enhancement in NIR PLQY for <b>Cu</b><sub><b>15</b></sub><b>-DPPB</b> (37.2% in nondegassed solution and 46% in the solid state at RT) versus <b>Cu</b><sub><b>15</b></sub><b>-TPP</b> (0.2% in solution), with emission maxima at ∼750 nm. The 37.2% PLQY of <b>Cu</b><sub><b>15</b></sub><b>-DPPB</b> is the highest reported for solution-phase NIR-emitting Cu-thiolate NCs. Excited-state dynamics studies unveil that this surface rigidification accelerates intersystem crossing (ISC) to populate triplet-state with boosted radiative decay (∼157-fold higher), and suppresses the nonradiative decay (∼0.53-fold lower). These findings demonstrate that ligand conformational engineering offers a new strategy to overcome intrinsic limitations of Cu-based emitters (e.g., weak spin-orbit coupling and slow intersystem crossing), and develop high-performance solution-phase RT NIR luminescent Cu NCs.
Authors
- Taeyeon Kim (ORCID: https://orcid.org/0009-0006-0054-5416)
- Zhong‐Hua Pan
- Geng‐Geng Luo (ORCID: https://orcid.org/0000-0003-4031-5632)
- Bao‐Liang Han (ORCID: https://orcid.org/0000-0002-4601-2600)
- Zeyu Liu (ORCID: https://orcid.org/0000-0002-7079-1907)
- Di Sun (ORCID: https://orcid.org/0000-0002-6688-5900)
- Lingyun Hu
- Zhi-Lin Yang
- Min Wei
Institutions
- Huaqiao University (CN)
- Shandong University (CN)
- Xiamen University (CN)
- Shantou University (CN)
- Ministry of Education (BD)
- Sungkyunkwan University (KR)
Publication Details
- Journal
- Journal of the American Chemical Society
- Published
- 2026-01-14
- DOI
- https://doi.org/10.1021/jacs.5c13894
- Citations
- 1
- Primary Topic
- Nanocluster Synthesis and Applications
- Type
- article
- Field-Weighted Citation Impact
- 16.08