Abstract

Controlling product selectivity in plasmonic catalysis, particularly in CO₂ reduction (CO₂R), remains a central unsolved challenge with direct implications for light-driven fuel and chemical synthesis. Here, we deploy quantitative operando scanning photoelectrochemical microscopy (photo-SECM) to provide a direct demonstration that tuning photon energy switches CO₂R selectivity through an electronically driven pathway. On plasmonic Au/p-GaN photocathodes, interband excitation (460-560 nm) drives selective CO production while intraband excitation (640-800 nm) favors H₂ evolution. By maintaining constant absorbed power across wavelengths and confirming linear power dependence, we isolate the role of hot-carrier energy from photonic and photothermal contributions. Density functional theory calculations reveal that higher-energy interband excitation progressively increases the overlap between hot-electron-accessible states and the CO-producing intermediate, selectively promoting CO over formate, in excellent agreement with experiment. We further show that selectivity is geometrically gated by hot-carrier transport: sub-100 nm nanostructures sustain CO₂R activity, while ~300 nm nanodisks suffer transport losses that suppress it, consistent with ab initio hot-carrier transport calculations. Together, these results establish photon energy, carrier transport, and nanostructure geometry as coupled design parameters for plasmonic CO₂R selectivity, resolve a longstanding debate on the origin of plasmon-driven selectivity effects, and position photo-SECM as a broadly applicable operando platform for photo(electro)catalysis.

Abstract

Controlling product selectivity in plasmonic catalysis, particularly in CO₂ reduction (CO₂R), remains a central unsolved challenge with direct implications for light-driven fuel and chemical synthesis. Here, we deploy quantitative operando scanning photoelectrochemical microscopy (photo-SECM) to provide a direct demonstration that tuning photon energy switches CO₂R selectivity through an electronically driven pathway. On plasmonic Au/p-GaN photocathodes, interband excitation (460-560 nm) drives selective CO production while intraband excitation (640-800 nm) favors H₂ evolution. By maintaining constant absorbed power across wavelengths and confirming linear power dependence, we isolate the role of hot-carrier energy from photonic and photothermal contributions. Density functional theory calculations reveal that higher-energy interband excitation progressively increases the overlap between hot-electron-accessible states and the CO-producing intermediate, selectively promoting CO over formate, in excellent agreement with experiment. We further show that selectivity is geometrically gated by hot-carrier transport: sub-100 nm nanostructures sustain CO₂R activity, while ~300 nm nanodisks suffer transport losses that suppress it, consistent with ab initio hot-carrier transport calculations. Together, these results establish photon energy, carrier transport, and nanostructure geometry as coupled design parameters for plasmonic CO₂R selectivity, resolve a longstanding debate on the origin of plasmon-driven selectivity effects, and position photo-SECM as a broadly applicable operando platform for photo(electro)catalysis.

Abstract

Controlling product selectivity in plasmonic catalysis, particularly in CO₂ reduction (CO₂R), remains a central unsolved challenge with direct implications for light-driven fuel and chemical synthesis. Here, we deploy quantitative operando scanning photoelectrochemical microscopy (photo-SECM) to provide a direct demonstration that tuning photon energy switches CO₂R selectivity through an electronically driven pathway. On plasmonic Au/p-GaN photocathodes, interband excitation (460-560 nm) drives selective CO production while intraband excitation (640-800 nm) favors H₂ evolution. By maintaining constant absorbed power across wavelengths and confirming linear power dependence, we isolate the role of hot-carrier energy from photonic and photothermal contributions. Density functional theory calculations reveal that higher-energy interband excitation progressively increases the overlap between hot-electron-accessible states and the CO-producing intermediate, selectively promoting CO over formate, in excellent agreement with experiment. We further show that selectivity is geometrically gated by hot-carrier transport: sub-100 nm nanostructures sustain CO₂R activity, while ~300 nm nanodisks suffer transport losses that suppress it, consistent with ab initio hot-carrier transport calculations. Together, these results establish photon energy, carrier transport, and nanostructure geometry as coupled design parameters for plasmonic CO₂R selectivity, resolve a longstanding debate on the origin of plasmon-driven selectivity effects, and position photo-SECM as a broadly applicable operando platform for photo(electro)catalysis.

Abstract

Controlling product selectivity in plasmonic catalysis, particularly in CO₂ reduction (CO₂R), remains a central unsolved challenge with direct implications for light-driven fuel and chemical synthesis. Here, we deploy quantitative operando scanning photoelectrochemical microscopy (photo-SECM) to provide a direct demonstration that tuning photon energy switches CO₂R selectivity through an electronically driven pathway. On plasmonic Au/p-GaN photocathodes, interband excitation (460-560 nm) drives selective CO production while intraband excitation (640-800 nm) favors H₂ evolution. By maintaining constant absorbed power across wavelengths and confirming linear power dependence, we isolate the role of hot-carrier energy from photonic and photothermal contributions. Density functional theory calculations reveal that higher-energy interband excitation progressively increases the overlap between hot-electron-accessible states and the CO-producing intermediate, selectively promoting CO over formate, in excellent agreement with experiment. We further show that selectivity is geometrically gated by hot-carrier transport: sub-100 nm nanostructures sustain CO₂R activity, while ~300 nm nanodisks suffer transport losses that suppress it, consistent with ab initio hot-carrier transport calculations. Together, these results establish photon energy, carrier transport, and nanostructure geometry as coupled design parameters for plasmonic CO₂R selectivity, resolve a longstanding debate on the origin of plasmon-driven selectivity effects, and position photo-SECM as a broadly applicable operando platform for photo(electro)catalysis.