Achieving control of light-material interactions for photonic device applications at nanoscale dimensions will require structures that guide electromagnetic energy with a lateral mode confinement below the diffraction limit of light. This cannot be achieved by using conventional waveguides or photonic crystals. It has been suggested that electromagnetic energy can be guided below the diffraction limit along chains of closely spaced metal nanoparticles that convert the optical mode into non-radiating surface plasmons. A variety of methods such as electron beam lithography and self-assembly have been used to construct metal nanoparticle plasmon waveguides. However, all investigations of the optical properties of these waveguides have so far been confined to collective excitations, and direct experimental evidence for energy transport along plasmon waveguides has proved elusive. Here we present observations of electromagnetic energy transport from a localized subwavelength source to a localized detector over distances of about 0.5 microm in plasmon waveguides consisting of closely spaced silver rods. The waveguides are excited by the tip of a near-field scanning optical microscope, and energy transport is probed by using fluorescent nanospheres.

Photosynthetic antenna complexes capture and concentrate solar radiation by transferring the excitation to the reaction center that stores energy from the photon in chemical bonds. This process occurs with near-perfect quantum efficiency. Recent experiments at cryogenic temperatures have revealed that coherent energy transfer-a wave-like transfer mechanism-occurs in many photosynthetic pigment-protein complexes. Using the Fenna-MatthewsOlson antenna complex (FMO) as a model system, theoretical studies incorporating both incoherent and coherent transfer as well as thermal dephasing predict that environmentally assisted quantum transfer efficiency peaks near physiological temperature; these studies also show that this mechanism simultaneously improves the robustness of the energy transfer process. This theory requires long-lived quantum coherence at room temperature, which never has been observed in FMO. Here we present evidence that quantum coherence survives in FMO at physiological temperature for at least 300 fs, long enough to impact biological energy transport. These data prove that the wave-like energy transfer process discovered at 77 K is directly relevant to biological function. Microscopically, we attribute this long coherence lifetime to correlated motions within the protein matrix encapsulating the chromophores, and we find that the degree of protection afforded by the protein appears constant between 77 K and 277 K. The protein shapes the energy landscape and mediates an efficient energy transfer despite thermal fluctuations.biophysics | photosynthesis | quantum beating | ultrafast spectroscopy | quantum biology E nergy transfer through photosynthetic pigment-protein complexes operates with exceptionally high quantum efficiency (1). Recent studies have demonstrated that energy moves through antennae using not only a classical hopping mechanism but also a manifestly quantum mechanical wave-like mechanism at cryogenic temperatures (2-5). Theoretical studies of this process within the Fenna-Matthews-Olson antenna complex (FMO) show that this quantum transport mechanism requires a balance between unitary (oscillatory) and dissipative (dephasing) dynamics; further, this balance appears to be optimized near room temperature and contributes to the robustness of the process (6-9). This theory demands that quantum coherence persist long enough to affect transport, but quantum beating has never been observed in FMO at physiological temperature.The FMO pigment-protein complex from Chlorobium tepidum serves as a model system for photosynthetic energy transfer processes (2, 10-13). This complex conducts energy from the larger light-harvesting chlorosome to the reaction center in green sulfur bacteria (14, 15). Each noninteracting FMO monomer contains seven coupled bacteriochlorophyll-a chromophores arranged asymmetrically, yielding seven nondegenerate, delocalized molecular excited states called excitons (11,16). The small number of distinct states makes this particular complex attractive for theoretical studies o...

Light-harvesting antenna complexes transfer energy from sunlight to photosynthetic reaction centers where charge separation drives cellular metabolism. The process through which pigments transfer excitation energy involves a complex choreography of coherent and incoherent processes mediated by the surrounding protein and solvent environment. The recent discovery of coherent dynamics in photosynthetic light-harvesting antennae has motivated many theoretical models exploring effects of interference in energy transfer phenomena. In this work, we provide experimental evidence of long-lived quantum coherence between the spectrally separated B800 and B850 rings of the light-harvesting complex 2 (LH2) of purple bacteria. Spectrally resolved maps of the detuning, dephasing, and the amplitude of electronic coupling between excitons reveal that different relaxation pathways act in concert for optimal transfer efficiency. Furthermore, maps of the phase of the signal suggest that quantum mechanical interference between different energy transfer pathways may be important even at ambient temperature. Such interference at a product state has already been shown to enhance the quantum efficiency of transfer in theoretical models of closed loop systems such as LH2.quantum biology | photosynthesis | ultrafast spectroscopy | biophysics | excitonic dynamics L ight-harvesting complex 2 (LH2) is the peripheral antenna pigment-protein complex of purple non-sulfur bacteria. LH2 contains two rings of BChl a pigments known as the B800 and B850 rings according to their respective room-temperature absorption bands in the infrared region of the spectrum (Fig. 1). These pigments are held in place by noncovalent interactions with pairs of low-molecular weight apoproteins. In most bacterial species, the LH2 complex consists of eight or nine of these protein heterodimers (αβ) organized in a highly symmetric ring (1). LH2 increases the effective cross-section for photon absorption from the solar spectrum in the membrane of purple bacteria. The energy absorbed by LH2 passes to another light-harvesting complex (LH1) tightly associated with the photosynthetic reaction center (2), wherein a stable charge separated state forms that ultimately drives the production of ATP.The energy transfer dynamics in LH2 has been studied for many years. Numerous time-resolved experiments have measured energy transfer from the B800 ring to the B850 ring in under a picosecond at room temperature (3-7). Förster resonance energy transfer (FRET) theory (8) estimates a slower transfer time by approximately a factor of five (9-13). Close examination of electronic coupling between pigments within each ring reveals, in part, the origin of this discrepancy. Studies on the excitation of the B850 ring (14-17) indicate the existence of Frenkel excitons (18,19), delocalized excitations that persist across several pigment molecules depending on the degree of structural symmetry present. In one limiting case, excitation is delocalized across the entire ring, invalidating a fundamen...

The Goldschmidt tolerance factor in halide perovskites limits the number of cations that can enter their cages without destabilizing their overall structure. Here we have explored the limits of this geometric factor and found that the ethylammonium (EA) cations which lie outside the tolerance factor range can still enter the cages of the 2D halide perovskites by stretching them. The new perovskites allow us to study how these large cations occupying the perovskite cages affect