Protecting groups in insertion chemistry: Site-selective positioning of lithium ions in intercalation hosts

The expanding toolbox of functionalization chemistries for selec-tively installing moieties on specific sites of a substrate underpins almost all modern organic and biochemical syntheses. Likewise, the installation of mobile guest ions in specific interstitial sites and their transport along specific diffusion pathways forms the basis of modern lithium (Li)-ion battery electrodes. Many insertion hosts afford a diverse range of accessible interstitial sites. However, site-selective positioning of cations with atomic precision remains almost entirely unexplored. Here, we show that by deciphering site preferences of co/pre-intercalated cations, we can position Li ions in four distinct sites within a 1D z-V2O5 insertion host. The use of topochemistry to effect single-crystal-to-single-crystal trans-formations enables atomic-resolution mapping of the selective posi-tioning of Li ions through single-crystal X-ray diffraction. We image interstitial sites that are occupied at high depths of discharge, thereby obtaining unprecedented structural insight into fully stuf-fedframeworks critical for the realization of high-energy-density intercalation electrodes.

Automated summary

The expanding toolbox of functionalization chemistries allows for selective installation of moieties on specific sites of a substrate, making it the foundation of modern organic and biochemical syntheses. In the field of lithium-ion battery electrodes, the installation of mobile guest ions in specific interstitial sites plays a crucial role. However, the site-selective positioning of cations with atomic precision is still unexplored. This study demonstrates the use of topochemistry to achieve site-selective positioning of Li ions in a 1D z-V2O5 insertion host, providing unprecedented structural insight into fully stuffed frameworks critical for high-energy-density intercalation electrodes.