To realize the full potential of solar energy, scientists must find efficient ways of converting light energy into chemical energy. In a recently published study, scientists from Nagoya Institute of Technology in Japan have developed a chemically modified variant of a photosynthetic enzyme sourced from a bacterium. Their modifications enabled the enzyme to more efficiently harvest the energy available in light, which is an important advancement in the development of clean solar energy.
Given the finite nature of fossil fuel reserves and the devastating environmental impacts of relying on fossil fuels, the development of clean energy sources is among the most pressing challenges facing modern industrial civilization. Solar energy is an attractive clean energy option, but the widescale implementation of solar energy technologies will depend on the development of efficient ways of converting light energy into chemical energy.
Like many other research groups, the members of Professor Takehisa Dewa’s research team at Nagoya Institute of Technology in Japan have turned to biological photosynthetic apparatuses, which are, in Prof. Dewa’s words, both “a source of inspiration and a target to test ways of improving the efficiency of artificial systems.”
Specifically, they chose to focus on the purple photosynthetic bacterium Rhodopseudomonas palustris, which uses a biohybrid light-harvesting 1–reaction center core complex (LH1-RC) to both capture light energy and convert it into chemical energy.
In their initial studies of R. palustris, Prof. Dewa’s group quickly noted that the LH1-RC system has certain limitations, such as only being able to harvest light energy efficiently within a relatively narrow wavelength band due to its reliance on (bacterio)chlorophylls, a single light-harvesting organic pigment assembly (B875, named for its absorption maximum).
To overcome this limitation, the researchers, in partnership with collaborators at Osaka University and Ritsumeikan University, experimented with covalently linking the LH1-RC system to a set of fluorophores (Alexa647, Alexa680, Alexa750, and ATTO647N). The results of their experiments appear in a paper published in a recent issue of the Journal of Photochemistry & Photobiology A: Chemistry.
Having synthesized their modified LH1-RC system, Prof. Dewa’s team used a method called “femtosecond transient absorption spectroscopy” to confirm the presence of ultrafast “excitation energy” transfer from the fluorophores to the bacteriochlorophyll a pigments in the B875 assembly. They also confirmed the subsequent occurrence of “charge separation” reactions, a key step in energy harvesting.
Unsurprisingly, the rate of excitation energy transfer increased with greater spectral overlap between the emission bands of the fluorophores and the absorption band of B875. Attaching the external light-harvesting fluorophores boosted the enzyme’s maximum yield of charge separation and photocurrent generation activity on an electrode within an artificial lipid bilayer system.
By introducing covalently linked fluorophores into a bacterial photosynthetic enzyme (as shown in Figure 1), Prof. Dewa’s team succeeded in broadening the enzyme’s band of harvestable light wavelengths. This is an important improvement given the extremely low energy density of sunlight.
“This finding could pave the way to developing an efficient artificial photosynthesis system for solar energy conversion,” notes Prof. Dewa. “Research on biohybrids should provide insights into the development of implementable energy conversion systems, thereby giving advanced modern civilization a practical option for accessing an inexhaustible supply of clean solar energy,” he adds.
The energy conversion systems in question may take many forms, including various nanomaterials, such as quantum dots and nanocarbon materials, but a unifying feature will be the need for some way to harness a broad-spectrum light-harvesting apparatus to a photocurrent-generating apparatus, and the biohybrid-type system developed by Prof. Dewa’s team provides a feasible means of addressing this need.