Related Experiment Video
Updated: Jun 26, 2026

Synthesis and Performance Characterizations of Transition Metal Single Atom Catalyst for Electrochemical CO2 Reduction
Published on: April 10, 2018
Dynamics of CO2 activation by gas-phase transition metal ions: the importance of intersystem crossing
Marcel Meta1, Yang Liu2, Hua Guo2
1Fachbereich Chemie und Forschungszentrum OPTIMAS, Rheinland-Pfälzische Technische Universität Kaiserslautern-Landau (RPTU), Erwin-Schrödinger Straße 52, 67663 Kaiserslautern, Germany. jennifer.meyer@chem.rptu.de.
Abstract:
The activation of CO2 at isolated transition-metal centers represents a prototypical problem for understanding elementary steps relevant to single-atom catalysis. Fundamental knowledge of such systems can be acquired by investigating gas phase reactions between transition-metal ions and molecules. Because open-shell transition-metal species often possess multiple accessible spin states, their reactions with CO2 can proceed along competing spin-changing and spin-conserving pathways. Understanding how spin-orbit coupling influences these competing pathways therefore calls for a direct comparison between scattering experiments and multi-state dynamical simulations. In this Perspective, we summarize our combined experimental and theoretical investigations of the Ta+, Nb+, and Zr+ + CO2 reactions. Crossed-beam velocity map imaging provides energy- and angle-resolved differential cross sections, while trajectory surface-hopping simulations on first-principles based full-dimensional multi-spin potential energy surfaces enable a dynamical treatment of intersystem crossing and spin-conserving channels on an equal footing. In all three systems, intersystem crossing competes with the spin-conserving channel for the control of the overall reaction dynamics and kinetics. These reactions all proceed predominantly via an indirect mechanism, as evidenced by the nearly isotropic differential cross sections consistent with long-lived complex formation, and the respective product energy distributions indicate substantial energy deposition into internal modes. Despite their similar potential-energy topographies, Ta+ and Nb+ + CO2 reactions are dominated by spin-changing pathways at all energies investigated, whereas in the Zr+ system the spin-conserving channel becomes competitive. This difference arises from the markedly different magnitudes of the spin-orbit coupling, which determines the efficiency of intersystem crossing and thereby the balance between the two pathways.
Related Concept Videos
Deactivation Processes: Jablonski Diagram
Crystal Field Theory - Octahedral Complexes
To explain the observed behavior of transition metal complexes (such as colors), a model involving electrostatic interactions between the electrons from the ligands and the electrons in the unhybridized d orbitals of the central metal atom has been developed. This electrostatic model is crystal field theory (CFT). It helps to understand, interpret, and predict the colors, magnetic behavior, and some structures of coordination compounds of transition metals.
CFT focuses on...
Valence Bond Theory
Transition State Theory
Properties of Transition Metals
Colors and Magnetism
When atoms or molecules absorb light at the proper frequency, their electrons are excited to higher-energy orbitals. For many main group atoms and molecules, the absorbed photons are in the ultraviolet range of the electromagnetic spectrum, which cannot be detected by the human eye. For coordination compounds, the energy difference between the d orbitals often allows photons in the visible range to be absorbed and emitted, which is seen as colors by the human eye.

