Electrochemical C-N Bond Formation within Boron Imidazolate Cages Featuring Single Copper Sites.

Electrocatalysis expands the ability to generate industrially relevant chemicals locally and on-demand with intermittent renewable energy, thereby improving grid resiliency and reducing supply logistics. Herein, we report the feasibility of using molecular copper boron-imidazolate cages, BIF-29(Cu), to enable coupling between the electroreduction reaction of CO2 (CO2RR) with NO3- reduction (NO3RR) to produce urea with high selectivity of 68.5% and activity of 424 µA cm-2. Remarkably, BIF-29(Cu) is among the most selective systems for this multistep C-N coupling to-date, despite possessing isolated single-metal sites. The mechanism for C-N bond formation was probed with a combination of electrochemical analysis, in situ spectroscopy, and atomic-scale simulations. We found that NO3RR and CO2RR occur in tandem at separate copper sites with the most favorable C-N coupling pathway following the condensation between *CO and NH2OH to produce urea. This work highlights the utility of supramolecular metal-organic cages with atomically discrete active sites to enable highly efficient coupling reactions.

CO2 Activation with Manganese Tricarbonyl Complexes through an H-Atom Responsive Benzimidazole Ligand.

Herein, we report the synthesis and characterization of two manganese tricarbonyl complexes, MnI (HL)(CO)3 Br (1 a-Br) and MnI (MeL)(CO)3 Br (1 b-Br) (where HL=2-(2'-pyridyl)benzimidazole; MeL=1-methyl-2-(2'-pyridy)benzimidazole) and assayed their electrocatalytic properties for CO2 reduction. A redox-active pyridine benzimidazole ancillary ligand in complex 1 a-Br displayed unique hydrogen atom transfer ability to facilitate electrocatalytic CO2 conversion at a markedly lower reduction potential than that observed for 1 b-Br. Notably, a one-electron reduction of 1 a-Br yields a structurally characterized H-bonded binuclear Mn(I) adduct (2 a') rather than the typically observed Mn(0)-Mn(0) dimer, suggesting a novel method for CO2 activation. Combining advanced electrochemical, spectroscopic, and single crystal X-ray diffraction techniques, we demonstrate the use of an H-atom responsive ligand may reveal an alternative, low-energy pathway for CO2 activation by an earth-abundant metal complex catalyst.

Guiding CO2RR Selectivity by Compositional Tuning in the Electrochemical Double Layer.

The electrochemical conversion of carbon dioxide to value-added chemicals provides an environmentally benign alternative to current industrial practices. However, current electrocatalytic systems for the CO2 reduction reaction (CO2RR) are not practical for industrialization, owing to poor specific product selectivity and/or limited activity. Interfacial engineering presents a versatile and effective method to direct CO2RR selectivity by fine-tuning the local chemical dynamics. This Account describes interfacial design strategies developed in our laboratory that use electrolyte engineering and porous carbon materials to modify the local composition at the electrode-electrolyte interface.Our first strategy for influencing surface reactivity is to perturb the electrochemical double layer by tuning the electrolyte composition. We approached this investigation by considering how charged molecular additives can organize at the electrode surface and impact CO2 activation. Using a combination of advanced electrochemical techniques and in situ vibrational spectroscopy, we show that the surfactant properties (the identity of the headgroup, alkyl chain length, and concentration) as well as the electrolyte cation identity can affect how surfactant molecules assemble at a biased electrode. The interplay between the electrolyte cations and the surfactant additives can be regulated to favor specific carbon products, such as HCOO-, and suppress the parasitic hydrogen evolution reaction (HER). Together, our findings highlight how molecular assemblies can be used to design selective electrocatalytic systems.In addition to the electrolyte design, the local spatial confinement of reaction intermediates presents another strategy to direct CO2RR selectivity. We were interested in uncovering the role of porous carbon-supported catalysts toward selective carbon product formation. In our initial study, we show that carbon porosity can be optimized to enhance C2H4 and CO selectivity in a series of Cu catalysts embedded in a tunable carbon aerogel matrix. These results suggested that local confinement of the active surface plays a role in CO2 activation and motivated an investigation into probing how this phenomenon can be translated to a planar Cu electrode. Our findings show that carbon modifiers facilitated surface reconstruction and regulated CO2 diffusion to suppress HER and improve the C2-3 product selectivity. Given the ubiquity of carbon materials in catalysis, this work demonstrates that carbon plays an active role in regulating selectivity by restricting the diffusion of substrate and reaction intermediates. Our work in tuning the composition of the electrochemical double layer for increased CO2RR selectivity demonstrates the potential versatility in boosting catalytic performance across an array of catalytic systems.

From Molecules to Porous Materials: Integrating Discrete Electrocatalytic Active Sites into Extended Frameworks.

Metal-organic and covalent-organic frameworks can serve as a bridge between the realms of homo- and heterogeneous catalytic systems. While there are numerous molecular complexes developed for electrocatalysis, homogeneous catalysts are hindered by slow catalyst diffusion, catalyst deactivation, and poor product yield. Heterogeneous catalysts can compensate for these shortcomings, yet they lack the synthetic and chemical tunability to promote rational design. To narrow this knowledge gap, there is a burgeoning field of framework-related research that incorporates molecular catalysts within porous architectures, resulting in an exceptional catalytic performance as compared to their molecular analogues. Framework materials provide structural stability to these catalysts, alter their electronic environments, and are easily tunable for increased catalytic activity. This Outlook compares molecular catalysts and corresponding framework materials to evaluate the effects of such integration on electrocatalytic performance. We describe several different classes of molecular motifs that have been included in framework materials and explore how framework design strategies improve on the catalytic behavior of their homogeneous counterparts. Finally, we will provide an outlook on new directions to drive fundamental research at the intersection of reticular-and electrochemistry.

Achieving spin-triplet exciton transfer between silicon and molecular acceptors for photon upconversion.

Inorganic semiconductor nanocrystals interfaced with spin-triplet exciton-accepting organic molecules have emerged as promising materials for converting incoherent long-wavelength light into the visible range. However, these materials to date have made exclusive use of nanocrystals containing toxic elements, precluding their use in biological or environmentally sensitive applications. Here, we address this challenge by chemically functionalizing non-toxic silicon nanocrystals with triplet-accepting anthracene ligands. Photoexciting these structures drives spin-triplet exciton transfer from silicon to anthracene through a single 15 ns Dexter energy transfer step with a nearly 50% yield. When paired with 9,10-diphenylanthracene emitters, these particles readily upconvert 488-640 nm photons to 425 nm violet light with efficiencies as high as 7 ± 0.9% and can be readily incorporated into aqueous micelles for biological use. Our demonstration of spin-triplet exciton transfer from silicon to molecular triplet acceptors can critically enable new technologies for solar energy conversion, quantum information and near-infrared driven photocatalysis.