Catalyst‐On‐Hotspot Nanoarchitecture: Plasmonic Focusing of Light onto Co‐Photocatalyst for Efficient Light‐To‐Chemical Transformation

• Published in: Small (Weinheim an der Bergstrasse, Germany) Vol. 20; no. 24; pp. e2309983 - n/a
• Main Authors: Chong, Carice, Boong, Siew Kheng, Raja Mogan, Tharishinny, Lee, Jinn‐Kye, Ang, Zhi Zhong, Li, Haitao, Lee, Hiang Kwee
• Format: Journal Article
• Language: English
• Published: Germany Wiley Subscription Services, Inc 01-06-2024
• Subjects: Catalysis; Catalysts; Chemical reactions; Copper oxides; Electromagnetic fields; electromagnetic hotspots; Focusing; Light; light‐concentrating effect; nanoarchitecture; Nanoparticles; Oxidation; Photocatalysis; photocatalyst; Photocatalysts; Plasmonics; Plasmons; plasmon‐mediated catalysis; Rate constants; Utilization; light-concentrating effect; photocatalyst; electromagnetic hotspots; plasmon-mediated catalysis; nanoarchitecture
• ISSN: 1613-6810; 1613-6829
• DOI: 10.1002/smll.202309983

Plasmon‐mediated catalysis utilizing hybrid photocatalytic ensembles promises effective light‐to‐chemical transformation, but current approaches suffer from weak electromagnetic field enhancements from polycrystalline and isotropic plasmonic nanoparticles as well as poor utilization of precious co‐catalyst. Here, efficient plasmon‐mediated catalysis is achieved by introducing a unique catalyst‐on‐hotspot nanoarchitecture obtained through the strategic positioning of co‐photocatalyst onto plasmonic hotspots to concentrate light energy directly at the point‐of‐reaction. Using environmental remediation as a proof‐of‐concept application, the catalyst‐on‐hotspot design (edge‐AgOcta@Cu2O) enhances photocatalytic advanced oxidation processes to achieve superior organic‐pollutant degradation at ≈81% albeit having lesser Cu2O co‐photocatalyst than the fully deposited design (full‐AgOcta@Cu2O). Mass‐normalized rate constants of edge‐AgOcta@Cu2O reveal up to 20‐fold and 3‐fold more efficient utilization of Cu2O and Ag nanoparticles, respectively, compared to full‐AgOcta@Cu2O and standalone catalysts. Moreover, this design also exhibits catalytic performance >4‐fold better than emerging hybrid photocatalytic platforms. Mechanistic studies unveil that the light‐concentrating effect facilitated by the dense electromagnetic hotspots is crucial to promote the generation and utilization of energetic photocarriers for enhanced catalysis. By enabling the plasmonic focusing of light onto co‐photocatalyst at the single‐particle level, the unprecedented design offers valuable insights in enhancing light‐driven chemical reactions and realizing efficient energy/catalyst utilizations for diverse chemical, environmental, and energy applications.
The strategic positioning of semiconductor co‐catalyst on the electromagnetic hotspots of anisotropic plasmonic nanoparticles is crucial to concentrate light directly at the point‐of‐reaction at the single‐particle level. This unique catalyst‐on‐hotspot design enables up to 20‐fold better utilization of catalytic materials and enhances catalysis by >4‐fold over emerging hybrid photocatalytic ensembles.