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Enhanced carbon capture and oxygen production via water splitting was observed by controlling the plasmon-induced resonance energy transfer (PIRET) for photosystem II (PSII) in thylakoid extracts and spirulina assembled on gold nanoparticle (AuNP) dimer arrays. The two types of vertical (V) and horizontal (H) AuNP dimer arrays were uniformly inserted inside pore diameter-controlled templates. Based on the theoretical calculations, the longitudinal mode of the H AuNP dimer array was found to be sensitive to the nanogap distances between the two AuNPs in resonance with the absorption at P680 of the PSII. The longitudinal modes that interacted with P680 of PSII increased from the V to the H conformer. The optical properties from the H AuNP dimer array caused overlapping absorbance and photoluminescence with PSII, and the H AuNP dimer arrays exhibited a significant increase in carbon capture and oxygen generation rates in comparison with those of the bare PSII protein complex under light irradiation via the controlled PIRET process.

We prepared novel Raman substrates for the sensitive detection of submicron-sized plastic spheres in water. Anisotropic nanostar dimer-embedded nanopore substrates were prepared for the efficient identification of submicron-sized plastic spheres by providing internal hot spots of electromagnetic field enhancements at the tips of nanoparticles. Silver-coated gold nanostars (AuNSs@Ag) were inserted into anodized aluminum oxide (AAO) nanopores for enhanced microplastic (MP) detection. We found that surface-enhanced Raman scattering (SERS) substrates of AuNSs@Ag@AAO yielded stronger signals at the same weight percentages for polystyrene MP particles with diameters as small as 0.4 μm, whereas such behaviors could not be observed for larger MPs (diameters of 0.8 μm, 2.3 μm, and 4.8 μm). The detection limit of the submicrometer-sized 0.4 μm in our Raman measurements were estimated to be 0.005% (∼0.05 mg/g =50 ppm) along with a fast detection time of only a few min without any sample pretreatments. Our nano-sized dimensional matching substrates may provide a useful tool for the application of SERS substrates for submicrometer MP pollutants in water.

Photoluminescence (PL) is the center property to deploy carbon quantum dots (CQDs) in diverse applications although their physicochemical origin is still debated. Herein, carboxylic-terminated CQDs were synthesized from citric acid (CA) and treated sequentially with ethylenediamine (EDA). Infrared, magnetic, X-ray photoelectron and UV–Vis spectroscopies indicated the formation of surface fluorophores by the EDA treatment. The post-decorated surface fluorophores accounted for a resolved UV absorption band at 346 nm, which originated from HOMO → LUMO transition in the fluorophores. The post-decorated fluorophores dominated the emission spectrum of CQDs when excited with wavelengths below 340 nm and enhanced the PL quantum yield of CQDs from 20.7% to 47.6%. The results pave new understanding on the optical properties of CQDs derived from CA and amines.