Yichao Jin, Keng‐Te Lin, Hongwei Liu, Ziqi Zhou, Xin Mao, Yanli Men, Wayde N. Martens, Tuquabo Tesfamichael, Sarina Sarina, Eric R. Waclawik, Aijun Du, Han Lin, Baohua Jia, Steven E. Bottle, H. Zhu
Photocatalytic ammonia synthesis is a potential alternative to Haber–Bosch but is limited by low solar-to-ammonia (STA) efficiency. We report a sunlight-driven, plasmonic antenna–reactor catalyst using just 0.1 wt % Ag deposited on a honeycomb AAO plate to form a ∼200 nm active layer. AAO pores trap/recycle light for photon-cascade harvesting, while >10 nm Ag “antennas” concentrate near-fields onto adjacent ≤5 nm Ag “reactors” enriched in low-coordination sites, directly coupling light capture to bond activation. Under concentrating natural sunlight (∼4 suns), the reactor self-heats to ∼150 °C at 0.5 MPa (1:3 N 2 /H 2 ) and achieves a high metal-normalized rate of 5.6 × 10 –3 s –1, exceeding industrial Fe at 450 °C/9 MPa on a metal-normalized basis. Under simulated sunlight (200 °C, 0.4 MPa), it reaches 159 mmol g Ag –1 h –1 for 200 h, with STA = 0.149% and AQE = 1.34% (575 nm). Density functional theory (DFT) and experiments support plasmon-assisted H 2 dissociation and associative N 2 hydrogenation (NNH*, N 2 H x ), overturning Ag’s presumed inertness.