Microalgae and cyanobacteria are some of nature’s finest examples of solar energy conversion systems, effortlessly transforming inorganic carbon into complex molecules through photosynthesis. The efficiency of energy-dense hydrocarbon production by photosynthetic organisms is determined in part by the light collected by the microorganisms. Therefore, optical engineering has the potential to increase the productivity of algae cultivation systems used for industrial-scale biofuel synthesis. Herein, we explore and report emerging and promising material science and engineering innovations for augmenting microalgal photosynthesis.
Photosynthesis is the model process for storing solar energy in complex chemical bonds. Annually it results in the fixation of upwards of 120 billion tons of carbon through terrestrial plants alone1, and nearly as much again inside the world’s oceans2. Humankind has sought over decades to mimic this process synthetically; however, to date, photosynthesis remains the only option for the sustainable production of many complex chemicals. In particular photosynthesis provides a sustainable path for the synthesis of high-energy-density liquid biofuels—an important priority in a world increasingly stressed by anthropogenic CO2. For these reasons, cultivation of photosynthetic plants and microalgae for biofuel production has attracted great interest.
Biofuel production from microalgae can follow several routes. Biodiesel can be produced by reacting triacylglycerols (a type of cellular energy storage lipid) with an alcohol, such as methanol, to produce fatty acid methyl esters (biodiesel), a process known as transesterification. For biodiesel production green algae and diatoms show particular promise as feedstocks owing to their high lipid concentration which can exceed 50% of the cell’s dry-weight3. In addition, microalgal carbohydrates can be converted to biomethane or biohydrogen, through anaerobic digestion or to bioethanol through fermentation4. Alternatively, raw biomass in its entirety can be converted into biocrude oil using thermochemical conversion processes such as pyrolysis or hydrothermal liquifaction4. To avoid harvesting and processing of raw biomass for biofuel extraction, direct photobiological production of hydrogen is possible with certain species, such as Chlamydomonas reinhardtii5. With genetic modifications, particularly of cyanobacteria, other biofuels and biofuel precursors can similarly be evolved including isobutyraldehyde6, isobutanol6, 1-butanol7 and isoprene8. Bio-electricity production in microalgal bio-photovoltaic cells has also been demonstrated9,10. This suite of microalgal energy generation options is a distinct advantage of photosynthesis over other solar energy conversion techniques which are typically constrained to generate only simple products, as in the case of photovoltaic electrolysis. The simultaneous production of a variety of co-products in addition to biofuel adds further value and flexibility to microalgal cultivation (Fig. 1; Box 1; Table 1). The generation of sufficient quantities of biomass is a prerequisite towards meeting large-scale demand and achieving economic viability, and is predicated on efficient sunlight utilization during cultivation. Present-day operations typically exhibit photosynthetic energy conversion efficiencies of about 1%, far short of the theoretical maximum of approximately 12% (ref. 11), owing to energy losses at all stages of the process (Fig. 1). As a result, industrial-scale cultivation of photosynthetic microorganisms has yet to achieve economic viability. Improving this efficiency is a multivariable problem, aspects of which have been previously discussed in several excellent reviews addressing microalgal culturing techniques12, economics13 and applications14.
In this review, we explore the latest optical engineering advances to manage light during microalgae cultivation to increase conversion efficiency and maximize productivity, summarized in Table 2. Latitude and weather determine the solar resources available and consequently the maximum productivity. The spectral distribution and intensity of light can be tuned using modern materials, reactor configurations and light sources, while mixing, culture density and light path lengths can be adjusted to optimize the light intensity experienced by the suspended cells, both spatially and temporally. In addition, the physical size and composition of the cellular light-harvesting apparatus itself can be tailored to enhance the spectral sensitivity and tolerance of cells to varying light environments. Material science, engineering and bioengineering approaches can provide elegant solutions to increase the efficiency of bioproduct production by photosynthetic organisms and potentially bypass the hurdles facing fully artificial photocatalytic devices.
Managing light collection
Reactor location selection
Solar resources vary by geographic region and are a determinant of a location’s suitability for microalgal culture. The simplest assessments of solar resources use clear sky irradiance models15, which primarily account for variation in solar flux due to atmospheric scattering which can reduce sunlight by a factor of around 83% at the equator (Fig. 1). Scattering losses, measured in terms of direct beam plus diffuse radiation, increase with distance from the equator incurring an additional efficiency factor of up to 70% at the poles. These models are limited in their predictive power however, because they overlook the impact of weather which can attenuate the available solar energy by a further factor of 35% (Fig. 1), based on measured monthly average irradiances (direct beam and diffuse) at several locations around the world, shown in Fig. 2a.
Site selection studies are therefore making increased use of historic meteorological data to project future solar resources in a region13,16. An assessment of Western Australia included average daily solar fluxes ranging between 150 and 277 W m−2, with over 90% of the continent between 208 and 277 W m−2 (ref. 17). This regional variation in sunlight can drive an increase in productivity from 3.6 to 7.7 g m−2 per day based on historical productivity observed in Chrysotila criteria and Tetraselmis spp17. Microalgae farming assessments in Chile identified primarily coastal desert regions as suitable locations for large-scale culture facilities using 165 W m−2 average annual irradiance as the threshold minimum18. Increasing access to historical irradiance data for thousands of locations worldwide has enabled greater insight into global weather trends and irradiances driving improvement in global site selection assesments19,20. Figure 2b shows a map of lipid productivity potential based on global irradiance data. Owing to high annual irradiances, minimal cloud cover and warm temperatures, equatorial locations have consistently shown the highest potential for microalgae cultivation21, correlating with the global trend in primary photosynthetic production (Fig. 2a)1. Based on growth models developed for Nannochloropsis sp. the global biomass production potential was estimated to be 9.4 g m−2 per day, with the maximum occurring in Australia (18 g m−2 per day) (ref. 21). The significant variation in solar resources by location makes these detailed site selections studies, which also account for other required resources (for example: water, carbon, labour and access to infrastructure), an important instrument in the planning and implementation of future microalgae cultivation projects.
Reactor orientation and solar tracking
Outdoor photobioreactors with typical cell density loading typically have light path lengths on the order of centimeters for enclosed photobioreactors, or tens of centimetres for open ponds (Fig. 2c–g)22. For flat plate designs (with large illuminated surface areas relative to their thickness) the direction in which they face is a significant factor in the amount of incident light they intercept. Models and tools for calculating the irradiance incident on a plane surface are now common in the solar energy field and can be used to calculate the irradiance potential for a given location and orientation23. An important difference is however, that unlike typical photovoltaic panels, photobioreactors are most often able to utilize light incident on both their front and back surfaces, allowing them to capture both direct and diffuse light.
Continuous tracking of the sun ensures maximal collection of sunlight. Based on clear sky models, the average annual intensity on a horizontal surface compared with a solar-tracked surface (example shown in Fig. 2g) is reduced by about 50% for latitudes of ±60° and about 77% at the equator (Fig. 1). Real-world examples of plate photobioreactors in France (47° N lat.) and Sudan (19 °N lat.) showed that horizontal reactors experienced 72 and 73% of the annual average irradiance seen by solar-tracked panel reactors, respectively20. In Germany (53 °N lat.), horizontal photobioreactors saw only 69% of the average annual irradiance seen by a solar-tracked photobioreactor24.
For stationary photobioreactors a vertical orientation facing east–west will generally intercept more light on average over the course of a year compared with both horizontal and north–south facing surfaces, as seen from clear sky models (Fig. 2a) and corroborating field tests which showed over 60% increased light harvesting during the summer for a location in Spain (37° N Lat.)25. Periodic adjustments in the orientation of flat plate reactors during the year can maximize the collected sunlight without the additional cost of continuous tracking26. For a site in Israel (31° N lat.), adjusting the tilt angle of a south facing flat plate reactor four times each year resulted in a 35% increase in productivity compared with a stationary horizontal reactor26.
The benefits of orienting a photobioreactor towards the sun to increase the amount of intercepted light are most simply realized for small-scale installations. For larger installations that involve arrays of reactors, the effect of shading between reactors becomes significant. While vertically oriented reactors intercept more light in isolation, they also create shaded areas limiting the light available to adjacent reactors. This shading can affect the productivity of large-scale installations and makes the spacing and height of individual reactors an important design criteria27,28. Furthermore, for these large installations the greater need for inter-reactor spacing results in additional loss when light falls upon the non-photosynthetic surfaces between reactors.
For large-scale systems, maximum light collection is most simply achieved through horizontal orientation of large area reactors or ponds, whereas for smaller single reactors or one-dimensional arrays where shading is of little concern, vertical orientation is preferred. Harvesting as much solar energy as possible is crucial for maximizing overall areal productivity, but high light intensity can also result in photoinhibition and energy loss through non-photochemical quenching pathways, reducing overall efficiency. Combining effective light collection with light distribution strategies, which will be discussed later in this review, is important to make full use of the collected photons.
Managing spectral distribution
Effect of spectral distribution
Once photons are intercepted by the cultivation apparatus, there is an opportunity to influence the spectral distribution of the transmitted photons. Photoautotrophs have evolved an array of light-harvesting pigments that can absorb energy across the visible spectrum, and the composition of these pigments determines the wavelengths that are absorbed for photosynthesis. Photosynthetically active radiation (PAR) is conventionally limited to wavelengths between 400 and 700 nm. This portion of the spectrum accounts for approximately 43% of the solar energy incident on earth and 28% of solar photons. Even though it is common to consider all PAR photons to be equally adept at driving photosynthesis, the array of chromophores involved in light harvesting and phytochromes involved in light sensing suggest a more complicated picture.
The action spectrum of photosynthetic organisms describes the rate of photosynthesis in response to light at different wavelengths29, and is typically determined by measuring autofluorescence, oxygen generation or growth rate under low-intensity monochromatic light. Figure 3a–e shows examples of both the absorption and action spectra for several macroalgae and microalgae species. In particular, Fig. 3 highlights the difference between a species’ ability to absorb specific wavelengths versus how well that species can utilize this absorbed light. Only a limited number of studies have measured the action spectrum for a small number of microalgae, while most others use the absorption or attenuation (absorption and scattering) spectrum as a proxy. Figure 3 shows however that there is often significant variation between the absorption and the absorbed action spectra for many classes of micro and macroalgae, and it is therefore important to note that wavelengths which may appear to be of low value based on poor absorption, may nevertheless play a substantial role in driving photosynthesis in optically thick cultures where all photons are ultimately absorbed30. For example, although the microalgae Nannochloropsis oculata (Fig. 3d) has a low absorption rate in the green region, it shows a noticeable peak in its absorbed action spectrum at these wavelengths31. In cultures of Scenedesmus bijuga and C. reinhardtii, green and yellow light respectively outperformed other wavelengths likely due to the combination of a deeper penetration depth for these poorly absorbed wavelengths and their ability to efficiently drive photosynthesis when they are finally absorbed30,32. For optically thin cultures however, the absorption spectra dictates the overall photon absorption of the culture at each wavelength and transmission of poorly absorbed light leads to lower performance at these wavelengths. For N. oculata, because blue light is strongly absorbed it resulted in the highest photosynthesis rate in optically thin cultures at low irradiances (60 μmolph m−2 s−1) (ref. 31). For practical applications however, cultures are usually fully absorbing and wavelengths between 500 and 650 nm are most efficient, particularly for cyanobacteria where shorter wavelengths often trigger photo-protection mechanisms.
Many photosynthetic organisms respond to changes in spectral distribution through sophisticated sensory mechanisms to preferentially express desirable metabolites33,34. Increased amounts of blue light have been shown to increase the expression of chlorophyll in Chlorella sp35 and lipids in both Tetraselmis sp. and Nannochloropsis sp36. Dynamically adjusting the wavelength distribution during cultivation can further enhance productivity. For Haematococcus pluvialis, red light promoted growth while blue light increased astaxanthin expression in the cells37. By culturing first with red light and then switching to blue, high biomass productivity and high astaxanthin concentrations were achieved. Similarly, a 20% enhancement in growth of Chlorella vulgaris was observed when grown with blue light for two days which resulted in an increase in average cell size, followed by red light for three days which increased the rate of cell division (Fig. 4a) resulting in an overall increase in productivity compared with control cultures38. These wavelength induced responses invite new avenues for tailored cultivation protocols using dynamic lighting to maximize production or expression of useful products.
In summary, the photosynthetic activity at any given wavelength is a complex coupling of the efficiency of transfer of the absorbed light energy by the light-harvesting pigments to the photosynthetic reaction centres (action spectrum), the fraction of incident light harvested by the cell (absorption spectrum), and the local light intensity which is affected also by culture density and depth. These relationships are further complicated by adaptation and photoinhibition responses that introduce second order dependencies on light intensity, spectral distribution and the physical environment. To leverage wavelength as a tool to maximize productivity in microalage, additional research needs to be conducted in a systematic fashion to elucidate these relationships more clearly, and define the action spectrum for a broader range of species and culture conditions.
High efficiency LED emitters (25%–66% W·W−1) (ref. 39) are now readily available and emit at wavelengths spanning the visible spectrum (Fig. 3f). Although other types of artificial illumination have been used for horticultural applications, including high-intensity discharge and fluorescent lamps, LEDs are expected to become dominant due to their long lifetimes, stability, low operating temperature, size and efficiency40. Benefits of LED light also include customization of the emitted spectrum and high degrees of spatial and temporal control which can compensate for the intensity, intermittency and day/night cycle of sunlight. Artificial light sources also allow culture vessels to be decoupled from the sunlight collection apparatus, simplifying temperature control, reactor geometry and making reactor positioning more manageable. Control of temperature is particularly important since the reaction rate and regulation of genes involved in the photosynthetic dark-reactions are strongly temperature dependant41. In temperate climates outdoor temperatures are often too low to support growth, and the costs of active temperature control for outdoor facilities are energetically and economically prohibitive. In warmer climates, operations may require cooling, which can introduce further challenges.
Energetically, LED-lit microalgal cultures can approach the net photosynthetic efficiencies achieved in outdoor pond reactors. Collecting solar energy with photovoltaic cells (18% efficient) connected to power high efficiency LEDs (approximately 46% efficient), net photosynthetic conversion efficiencies of about 1% could be achieved42, which accounts also for the efficiencies of photosynthesis and biosynthesis/maintenance (considered to be 27% and 50%, respectively—see Fig. 1). Photovoltaic electricity generation allows for a direct sunlight-to-biomass efficiency comparison, though on-sight solar farms are not likely feasible. For practical applications, it is more likely however that electricity to operate the LED’s would be purchased. Based on a typical cost of electricity of $0.10 per kW·h, an electricity-to-light conversion efficiency of 40%, a light-to-biomass conversion efficiency of 13.5% (27% for photosynthesis and 50% for biosynthesis and maintenance), and a biomass energy content of 23 kJ per gdry weight (ref. 43) the electricity cost of LED grown microalgae is estimated around $14 per kgdry weight, which is in agreement with previous studies42. This represents a cost of approximately $3,800 per barrel of oil equivalent, two orders of magnitude greater than the price of oil. Clearly, this cost is unacceptable for the production of low-value biofuels. For high-value bioproducts however, and applications with additional value streams such as flue gas or wastewater remediation, the economics improve. For example, astaxanthin can be harvested from H. pluvialis in concentrations of 2.5% dry weight or more, and sold for $2,000–$7,000 per kg resulting in a biomass value of $50–$175 per kgdry weight. Pond Biofuels (Toronto, Ontario) currently uses LED-lit microalgal cultures to capture CO2 from cement plant emissions. In such instances, the additional benefits and convenience of artificial illumination may justify the added expense while still remaining profitable42,44.
Though commercial applications for LED-lit photobioreactors are limited, LEDs have become ubiquitous in lab-scale microalgal research. Care needs to be taken however when, extrapolating results to outdoor reactors as artificial light sources have spectral distributions and irradiance profiles that differ from solar irradiance (Fig. 3f,g). In addition, measured light intensity emitted from artificial sources can vary widely owing to the distance dependence of LED lights which are typically point sources, intensity scaling inversely with distance cubed. Using arrays of LEDs, collimating optics, or diffusers can help homogenize the light field, but the detailed optics of these configurations are not often reported33. Control experiments typically involve white LEDs or fluorescent lamps which can have a range of emission spectra, most of which are poor approximations of sunlight33, as shown in Fig. 3g. Additional rigour in addressing and reporting the optical controls and parameters used in microalgae studies should be asserted more consistently in future work.
Wavelength shifting materials
Converting photons from one wavelength to another using fluorescent or phosphorescent materials can produce a spectrum amenable to increased growth or metabolite expression45. Organic and inorganic dyes, phosphors and quantum dots are promising candidates for converting light with little or no photosynthetic potential into light with higher photosynthetic potential46. Ideally, materials should be both highly absorbing to harvest a meaningful amount of light, exhibit high conversion efficiencies and have emission spectra sufficiently separate from their absorption spectra so as to avoid reabsorption of converted light.
Down-conversion of light incurs an energy penalty. Nevertheless, the opportunity to harvest photons that would otherwise not be available for photosynthesis is compelling. Most notably, ultraviolet light which is generally detrimental to growth can be converted to visible light usable for photosynthesis. For low-density cultures, converting poorly absorbed light to highly absorbed light (such as green to red) also improves light capture efficiency. For high-density cultures, converting blue light to green can provide greater light penetration into the culture by increasing the fraction of highly penetrating wavelengths, and mitigating the effects of light saturation under high-intensity illumination.
Wavelength shifting of incident light has typically been tested using discrete layers of fluorescent or phosphorescent materials. These converting layers are positioned either between the culture and light source (front-side conversion)47,48, or behind the culture to capture and convert transmitted light45. The latter configuration can be augmented with a reflective backing to reflect all transmitted and converted light back towards the culture, though, is useful only for dilute cultures where a meaningful amount of light can reach the dye layer. An example of this approach is highlighted in Fig. 4b, where a photoluminescent phosphor coated mirror back-plate was used to culture H. pluvialis and resulted in 36% more biomass generation at low densities.
For larger scale, outdoor installations, front-side conversion is a more practical approach since typical culture densities do not allow significant light transmission. To date, limited success has been seen growing and expressing pigments in C. vulgaris and cyanobacteria Gloeothece membranacea using luminescent acrylic sheets to increase the ratio of various portions of the spectrum49. Ultraviolet converting dyes entrained in the photobioreactor material can be used harvest and convert ultraviolet light that would otherwise be absorbed by the reactor (or transmitted to the culture) into visible light50,51. Examples of this approach have shown a 74% increase in biomass productivity when polycarbonate front-side ultraviolet converters were used and illuminated with ultraviolet light, and a 45% increase when acrylic converters were used50.
Of particular importance is the efficiency of the spectral tuning layer with respect to light directed towards the cell culture. Many wavelength shifting materials report high internal quantum efficiencies; however, these efficiencies are determined using monochromatic excitation and low concentrations of dye meaning only a small amount of incident light in actually converted. External quantum efficiencies can fall far short of these values as the emitter concentration increases to meaningful densities, due to reabsorption and scattering losses. Furthermore, unless sub-saturating light is used, it is difficult to disambiguate the impact of light attenuation (which alone will have a positive effect on photosynthetic efficiency), and the additional benefit of spectral tuning. Continued work in this field should assess these factors more rigorously, and focus on developing/utilizing the highest performing materials, particularly those that can convert non-PAR photons into PAR photons, with minimal attenuation of visible light.
When photons interact with the conduction electrons in metals or metallic nanoparticles, collective oscillations of the electrons can result, called surface plasmons. Exciting surface plasmons in metals significantly enhances the electromagnetic field in the vicinity of the metal surface or particle leading to enhanced absorption or scattering at specific resonant wavelengths. The precise nature and magnitude of these effects is a function of the material type, size, shape and the surrounding media. These optical effects have previously been used to enhance photo-conversion in other fields, particularly photovoltaics, by encouraging useful wavelengths to be redirected into, or confined within, the active media—whether biological or synthetic.
Plasmon enhanced fluorescence has been the subject of intensive research, and recently has been applied to the excitation of the photosynthetic apparatus in whole cells52. High-density cyanobacteria biofilms were cultivated in the presence of plasmonically enhanced electromagnetic fields on thin metallic films52 in which both light and the cells were confined to the substrate surface. Plasmonic scattering of light can also assist in containing specific wavelengths within photobioreactors53,54,55,56. C. reinhardtii and Cyanothece 51142 showed 30% increased biomass production when plasmonic layers made of silver nanoparticle suspensions scattered blue light back towards the cells54. Combinations of nanoparticles with different geometries and materials can produce complex scattering spectra to induced expression of desired metabolites55. Nanoparticles adhered to a reactor surface instead of suspended in a solvent can provide similar spectral effects but with greater mechanical stability. For instance, arrays of gold nanodisks on glass substrates have enhanced the growth of cyanobacterium S. elongatus (Fig. 4c)56. The plasmonic substrates reflected 35% of the red light transmitted through a dilute culture back into the reactor while allowing other wavelengths to be transmitted. This approach allowed for photosynthetically useful light to be returned to the culture while permitting shorter wavelengths to be transmitted for use in photovoltaics56. Energy loss from ohmic resistance in plasmonic metals however, remains a significant challenge for plasmonic technologies and, together with cost, will limit the usefulness of plasmonic light management in photobioreactors going forward in all except very niche applications.
Managing light distribution
Culture density and path length
Photosynthetic organisms are limited in the rate at which they utilize absorbed light. When light intensity drops below a certain compensation intensity, photosynthesis is outpaced by respiration and the organism will become a net consumer of oxygen and high energy compounds to maintain metabolism through the dark period. This dark respiration for cell maintenance and biomass synthesis often results in a net decrease in biomass as carbohydrates are consumed to support these cellular processes, but not replenished through photosynthesis. The rate of dark respiration relative to growth varies between species but is typically between 20 and 30% of an organism’s growth rate at the beginning of a dark period and declines with increasing dark exposure time, over the course of hours57. Similarly, under high irradiances, light saturation can occur. Saturation intensities vary widely but are typically around 150–400 μmolPAR m−2 s−1 (refs 58, 59). When the saturation limit is reached, excess energy is dissipated as heat and fluorescence60, and many species will initiate photo-protection mechanisms to prevent a buildup of harmful reactive oxygen species produced by photosynthesis41,60. Because most microalgal species saturate at intensities close to 10% of peak sunlight, during much of the day they operate at low photosynthetic efficiency—absorbing but not effectively using incoming radiation. To manage high intensities, biomass density, light path length and mixing rates can be selected to optimize productivity and mitigate the effects of photoinhibition from excess light.
While no universal rules for optimal path length and density apply across all species, some general trends have emerged that result in improved performance. Under high-intensity sunlight, optimal productivity often results from a combination of path length, density and mixing rate such that the frequency of cycling between the light and dark regions is on the same timescale as the turnover rate of the photosynthetic machinery, an effect demonstrated in several species61,62,63,64,65. It has been proposed that the flashing light effect can mitigate photoinhibition by providing a dark period of sufficient length to allow the electron transporters involved in shuttling electrons between reaction centres time to reoxidize41,58, thereby avoiding the need to exhaust energy through non-photosynthetic quenching pathways. Efficiency generally increases with pulse frequencies of 10–100 Hz (Fig. 5a)61. Similarly for saturating light, pulse times on the order of 1–10 ms followed by dark periods on the order of tens of milliseconds tend to be optimal61,62,63,66. In this way, productivity approaching the productivity of continuous light at the same time-averaged intensity can be achieved (full-light integration), even when the absolute intensity of the pulsed light is beyond the saturating intensity of the organism. Because the time-averaged intensity is necessarily less than the surface irradiance, the overall photosynthetic efficiency for the culture will be greater.
Studies exploring the flashing light effect have typically relied on pulsed LED light to simulate the cycling of cells between light and dark zones in a photobioreactor and have shown full-light integration to occur for species such as C. reinhardtii at frequencies greater than 50 Hz (ref. 61), and 10 Hz for Nannochloropsis salina67. The conditions under which light integration occurs and its extent is expected to vary between species and only a limited number have been evaluated. The diatom, Phaeodactylum tricornuturn, for instance, has achieved full-light integration at the much lower frequencies of 1 Hz (ref. 68). In photobioreactors where light–dark cycling is a function of geometry, cell density, and mixing, practical cycle frequencies are limited to less than 5 Hz (refs 64, 69, 70). In these contexts, only partial light integration is expected to occur, but can nevertheless result in a meaningful improvement in productivity and efficiency provided that culture density, path length and mixing rate are selected in concert to provide the optimal light regime and hydrodynamics64,67,71,72. Figure 5b shows an example of how productivity depends, for instance, on culture density for different light intensities72. High-density cultures and path lengths on the order of millimetres have been recommended to achieve the necessary cycle frequencies. Outdoor, high-density (6 g L−1) cascade reactors cultivating Chlorella sp., similar to the one shown in Fig. 5c73, have shown considerable improvements in productivity over more dilute installations and operate with culture depths of 6mm resulting in cycle frequencies of around 0.5 Hz (ref. 74). It has also been suggested that designing the system such that the time-averaged light intensity is close to but not exceeding the saturating intensity of the cells would maximize productivity and photosynthetic efficiency61.
Although alternating light–dark cycles have been shown to improve productivity for several species of interest, for others it has shown only marginal improvement75,76,77. As yet it is unclear whether these empirical observations are characteristic of the species, or due to variations in experimental conditions including reactor configuration, mixing strategy, species-dependent maintenance energy requirements, spectral distribution and cultivation history. Second order effects such photo-acclimation and protection mechanisms can further obfuscate the optimization process78. For instance, cells immobilized in high-density biofilms and exposed to high light showed a reduction in chlorophyll concentration, reducing absorption in the biofilm and allowing light to penetrate deeper and dynamically changing the illumination profile (Fig. 5d)79. Further research and consistency in experimental techniques is required to bring clarity to the mixed empirical results available to date.
An optical approach to managing high-intensity light is to dilute it over a larger surface area, thus reducing the local light intensity to productive levels. The curved surfaces of tubular photobioreactors are perhaps the simplest approach and can dilute incident light by a factor of 1.57 (refs 80, 81). Reactor orientation, as discussed previously, can also be adjusted to dilute light over a larger surface area of the reactor by changing the angle of the illuminated surface relative to the sun, such that the intensity will be proportional to the cosine of this angle. Obliquely incident light incurs additional losses related to Fresnel reflections at the interface between the environment and reactor surfaces. These losses are greatest at larger incident angles and at interfaces between materials with large refractive index contrasts, such as air (n=1) and glass (n=1.5).
Incorporation of transparent panels or waveguides into the culture volume is another light dilution approach (Fig. 5e)82,83,84. Biofilm photobioreactors (in which cells are cultivated as surface attached colonies rather than in suspension, (Fig. 5f) can particularly benefit from larger surface areas since more illuminated area is available for attachment and cultivation85,86. Roughened optical fibres have been used for this purpose to distribute light to biofilms attached to the fibre surfaces, and achieved light energy to hydrogen conversion efficiencies of 9.3% compared with 3.9% for cultures in suspension87. Similarly, stacks of optical waveguides have been used to distribute light to ultra-high-density cultures with path lengths of 2 mm and achieved an eightfold improvement in productivity over bulk cultures with a path length of 30 mm (ref. 85). Achieving uniform scattering of light from waveguides is desirable and can be achieved through patterned or random surface treatments88, though complete uniformity may not be necessary provided the peak intensity is below the saturation threshold.
Managing cellular light utilization
Engineering the molecular structure of the cellular light-harvesting apparatus presents genetic-engineering opportunities for efficiency improvement89. Excitation energy transfer to the reaction centres happens within 100 ps with efficiencies of 80%–100% (ref. 90), however, the slower enzyme-mediate reactions involved with water oxidation, electron transport and carbon fixation, can introduce bottlenecks particularly under high light. These bottlenecks can be avoided by reducing the photon absorption rate, which can be accomplished by reducing the size and absorption cross-section of the light-harvesting complex91.
For sub-saturating intensities, photosynthetic efficiency can be improved by increasing the spectral sensitivity of the light-harvesting apparatus to utilize a larger portion of the spectrum. This can be accomplished by engineering the pigment composition of the light-harvesting complexes making more wavelengths available for photosynthesis89. Control over spectral sensitivity as well as photo-protective mechanisms (which tend to direct energy towards non-photosynthetic channels) can be achieved by synthetically accessorizing light-harvesting antennae with additional carotenes and xanthophylls90. This approach represents a synthetic variation of the natural photo-adaptive responses of plants and microalgae in which pigments re-organize in response to changing light conditions92. Making more photons available for photosynthesis is advantageous provided photoinhibition by light saturation is avoided; strategies that rely on increasing absorption must simultaneously manage the incident photon flux.
Light harvesting and energy transduction at the cellular level can also leverage recent advances in nanomaterials. For example, single-walled carbon nanotubes have been inserted and irreversibly localized within the lipid envelope of isolated plant chloroplasts to assist with electron transport93. The result was a threefold increase in photosynthetic activity compared with unmodified chloroplasts. Light-harvesting nanocrystals have been grown on the surface of non-photosynthetic bacteria to generate electron–hole pairs and transfer these excited carriers directly to the cell for use in acetic acid synthesis94. Conversion efficiencies close to 80% were achieved under low light intensity by utilizing highly absorbing nanocrystals that feed charge-carriers to the high efficiency Wood-Ljungdahl acetic acid synthesis pathway. These studies, while still at the proof-of-concept stage, point towards the emerging opportunities for nanotechnology-augmented photosynthesis.
Alternative avenues of solar conversion via photosynthesis are emerging, many of which draw inspiration from nature in an engineering-biology-materials partnership. For example, charge-carriers generated through microalgal photosynthesis have been captured and used directly to power electrical devices9. The efficiency of these bio-photovoltaic cells, while still relatively low, is increasing, and may approach that of other photobiological and photovoltaic technologies9. Another hybrid system combines silicon nanowire arrays with bacteria to generating acetic acid95. Reducing equivalents generated by solar energy incident on the silicon nanowires are used by surface adhered bacteria to metabolize CO2. Future embodiments involving multiple, genetically tailored, bacteria could then use this acetic acid as a substrate to produce a range of useful polymers, biofuels and pharmaceutical precursors95.
Efficiently navigating the conversion of sunlight into value-added products is a key challenge for commercially viable bioproducts from microalgae, in particular for biofuels where margins are low. Incumbent global and regional energy systems are entrenched with decades and even centuries of experience, innovation, investment and infrastructure. The unprecedented success of fossil fuels puts a tremendous burden on emerging technologies in a market that is not fully motivated to seek alternatives. Fortunately, low-value biofuels can be co-produced with higher value but low-volume products14. For example, microalgae are a source of polyunsaturated fatty acids which are used in nutraceuticals, animal feedstocks, infant formulas and aquaculture. Carotenoids such as beta-carotene and astaxanthin are useful as food colourants and nutraceuticals. Phycobilins, which occur exclusively in microalgae, are valuable as fluorescent markers for laboratory and therapeutic purposes, and as natural food and cosmetic colourants. Biodegradable polymers can be made from polyhydroxyalkanoate, a polyester expressed by some bacteria and genetically modified macroalgae96. Co-production of useful high-value products with high-energy-density fuels can support the continued development of economical cultivation and processing technologies. Co-production is also an advantage photosynthesis demonstrates over other solar-fuel generation techniques. For instance photovoltaic-powered water electrolysis which has a similar theoretical energy conversion efficiency of around 13% (20% photovoltaic energy conversion efficiency, 65% electrolyser efficiency) is constrained to produce only hydrogen. Other photovoltaic-powered electrolysis such as electro-reduction of CO2 produces CO as main product with a solar-to-fuel conversion efficiency lower than 10% (ref. 97). Similarly, while photovoltaic cells have achieved over 40% efficiency, electricity is untenable for many applications particularly those requiring high-energy density such as transportation or long-term storage.
The ultimate practicality of each of the techniques discussed in this review is a function of implementation feasibility, cost and product value. Specifically, site selection considerations have much in common with photovoltaic light harvesting, and synergies between these two fields should be exploited, including design and modelling tools. Artificial light, in particular LEDs, are not currently practical for commodity production, but the production of high-value, low-volume compounds is feasible in the near-term and will support technology maturation. Further work to understand the combined effects of light spectrum distribution, intensity and physical/chemical environments is needed for a wider range of species, using consistent and systematic methods. To conduct these experiments, in high numbers and with the needed control, parallelization will be required beyond that of flask-based approaches applied to date65. Wavelength shifting materials hold a promise to increase the fraction of sunlight available for photosynthesis, though practical implementations which avoid reabsorption and scattering losses have not been forthcoming. Improved materials and incorporation of these materials into innovative reactor geometries are required to push photosynthetic efficiencies beyond the current theoretical limits. Other approaches to light spectrum management, such as plasmonic scattering, will only be viable provided that significant modification of the light spectrum can be achieved while internal losses remain low. This is a challenge in many optical systems, but plasmonics in particular.
Looking forward, we see three major opportunities for integrating the best photon management strategies in developing photobioreactor operations. First, advanced materials for customizing the spectrum of light incident on the cultures will enable production of specific bioproducts. So far, these effects have been studied in only a relatively small number of organisms and additional work is needed to understand the effects of spectral distribution on a wider range of organisms. Second, the economic potential of microalgal cultivation will be made clearer by designing cultivation schemes which are integrated with infrastructures able to provide supplies of carbon and nutrients, such as flue gas or municipal wastewater systems. This type of integration and context-specific assessment will quantify the ancillary benefits of mitigating and utilizing waste streams, adding value to the microalgal cultivation process. Further integration and development of on-site biomass processing technology such as hydrothermal liquefaction of algal biomass can provide insight into the full life-cycle efficiency of microalgal biofuel production. Third, better coordination and partnerships between pilot scale plant operators and academia will avail the latest developments to industry, provide for more consistent data collection and reporting of key performance metrics, and focus the efforts of academia on the specific constraints affecting the success of early pilots.
How to cite this article: Ooms, M. D. et al. Photon management for augmented photosynthesis. Nat. Commun. 7:12699 doi: 10.1038/ncomms12699 (2016).