Dear CP2K developers and users, Hello everyone, I am currently working on the Pourbaix diagram of lanthanide elements and would like to use CP2K to perform hybrid functional calculations for La₂O₃ and CeO₂. However, since there are no default ADMM basis sets available for lanthanides, the calculations are extremely slow—to an extent that is hardly acceptable. For systems doped with La and Ce, I managed to proceed by using the auxiliary basis sets of La and Ce as the primary basis sets. Although this approach also slows down the calculation, it is still acceptable. However, when it comes to hybrid functional calculations for pure La₂O₃ and CeO₂, the computation becomes practically infeasible. What should I do in such a situation? I found the def2-SVP basis set on the website <a href="https://www.basissetexchange.org/" target="_blank">https://www.basissetexchange.org/</a>, and I’ve heard that this basis set should be used together with the SDD pseudopotential. May I ask a beginner-level question: where can I download the SDD pseudopotential? Is it the same as the ECP_POTENTIAL pseudopotential provided in the CP2K folder? I would greatly appreciate any guidance or suggestions from the community. Thank you all in advance for your help! -- You received this message because you are subscribed to the Google Groups "cp2k" group. To unsubscribe from this group and stop receiving emails from it, send an email to <a href="mailto:cp2k+unsubscribe@googlegroups.com">cp2k+unsubscribe@googlegroups.com</a>. To view this discussion visit <a href="https://groups.google.com/d/msgid/cp2k/4dfbd57d-a432-4d2f-96fc-6696967ab827n%40googlegroups.com?utm_medium=email&utm_source=footer">https://groups.google.com/d/msgid/cp2k/4dfbd57d-a432-4d2f-96fc-6696967ab827n%40googlegroups.com</a>.