Evaluation of ultrasmall coinage metal M13(dppe)6 M = Cu, Ag, and Au clusters. Bonding, structural and optical properties from relativistic DFT calculations

Ultrasmall ligand-protected clusters are prototypical species for evaluating the variation at the bottom of the nanoscale range. Here we explored the ultrasmall gold-phosphine M-13(dppe)(6) cluster, as a prototypical framework to gain insights into the fundamental similarities and differences between Au, Ag, and Cu, in the 1-3 nm size range, via relativistic DFT calculations. Different charge states involving 8- and 10-cluster electron (ce) species with a 1S(2)1P(6) and 1S(2)1P(6)1D(2) configuration, leading to structural modification in the Au species between Au-13(dppm)(6)(5+) and Au-13(dppm)(6)(3+), respectively. Furthermore, this structural distortion of the M-13 core is found to occur to a lower degree for the calculated Ag and Cu counterparts. Interestingly, optical properties exhibit similar main patterns along with the series, inducing a blue-shift for silver and copper, in comparison to the gold parent cluster. For 10-ce species, the main features of 8-ce are retained with the appearance of several weak transitions in the range. The ligand-core interaction is enhanced for gold counterparts and decreased for lighter counterparts resulting in the Au > Cu > Ag trend for the interaction stabilization. Hence, the Ag and Cu counterparts of the Au-13(dppm)(6) cluster appear as useful alternatives, which can be further explored towards different cluster alternatives for building blocks for nanostructured materials.

Automated summary

By utilizing relativistic DFT calculations, the study explored the ultrasmall gold-phosphine cluster to investigate similarities and differences among Au, Ag, and Cu in the 1-3 nm size range. The structural distortion is found to be most prominent for gold species, while silver and copper exhibit blue-shift in their optical properties compared to gold.