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Solar reforming is the sunlight-driven conversion of diverse carbon waste resources (including solid, liquid, and gaseous waste streams such as biomass, plastics, industrial by-products, atmospheric carbon dioxide, etc.) into sustainable fuels (or energy vectors) and value-added chemicals. [1] It encompasses a set of technologies (and processes) operating under ambient and aqueous conditions, utilizing solar spectrum to generate maximum value. [1] Solar reforming offers an attractive and unifying solution to address the contemporary challenges of climate change and environmental pollution by creating a sustainable circular network of waste upcycling, clean fuel (and chemical) generation and the consequent mitigation of greenhouse emissions (in alignment with the United Nations Sustainable Development Goals).
The earliest sunlight-driven reforming (now referred to as photoreforming or PC reforming which forms a small sub-section of solar reforming; see Definition and classifications section) of waste-derived substrates involved the use of TiO2 semiconductor photocatalyst (generally loaded with a hydrogen evolution co-catalyst such as Pt). Kawai and Sakata from the Institute for Molecular Science, Okazaki, Japan in the 1980s reported that the organics derived from different solid waste matter could be used as electron donors to drive the generation of hydrogen gas over TiO2 photocatalyst composites. [2] [3] In 2017, Wakerley, Kuehnel and Reisner at the University of Cambridge, UK demonstrated the photocatalytic production of hydrogen using raw lignocellulosic biomass substrates in the presence of visible-light responsive CdS|CdOx quantum dots under alkaline conditions. [4] This was followed by the utilization of less-toxic, carbon-based, visible-light absorbing photocatalyst composites (for example carbon-nitride based systems) for biomass and plastics photoreforming to hydrogen and organics by Kasap, Uekert and Reisner. [5] [6] In addition to variations of carbon nitride, other photocatalyst composite systems based on graphene oxides, MXenes, co-ordination polymers and metal chalcogenides were reported during this period. [7] [8] [9] [10] [11] [12] [13] [14] A major limitation of PC reforming is the use of conventional harsh alkaline pre-treatment conditions (pH >13 and high temperatures) for polymeric substrates such as condensation plastics, accounting for more than 80% of the operation costs. [15] This was circumvented with the introduction of a new chemoenzymatic reforming pathway in 2023 by Bhattacharjee, Guo, Reisner and Hollfelder, which employed near-neutral pH, moderate temperatures for pre-treating plastics and nanoplastics. [16] In 2020, Jiao and Xie reported the photocatalytic conversion of addition plastics such as polyethylene and polypropylene to high energy-density to C2 fuels over a Nb2O5 catalyst under natural conditions. [17]
The photocatalytic process (referred to as PC reforming; see Categorization and configurations section below) offers a simple, one-pot and facile deployment scope, but has several major limitations, making it challenging for commercial implementation. [15] In 2021, sunlight-driven photoelectrochemical (PEC) systems/technologies operating with no external bias or voltage input were introduced by Bhattacharjee and Reisner at the University of Cambridge. [18] These PEC reforming (see Categorization and configurations section) systems reformed diverse pre-treated waste streams (such as lignocellulose and PET plastics) to selective value-added chemicals with the simultaneous generation of green hydrogen, and achieving areal production rates 100-10000 times higher than conventional photocatalytic processes. [18] In 2023, Bhattacharjee, Rahaman and Reisner extended the PEC platform to a solar reactor which could reduce greenhouse gas CO2 to different energy vectors (CO, syngas, formate depending on the type of catalyst integrated) and convert waste PET plastics to glycolic acid at the same time. [19] This further inspired the direct capture and conversion of CO2 to products from flue gas and air (direct air capture) in a PEC reforming process (with simultaneous plastic conversion). [20] Choi and Ryu demonstrated a polyoxometallate-medated PEC process to achieve biomass conversion with unassisted hydrogen production in 2022. [21] Similarly, Pan and Chu, in 2023 reported a PEC cell for renewable formate production from sunlight, CO2 and biomass-derived sugars. [22] These developments has led solar reforming (and electroreforming, where renewable electricity drives redox processes; see Caterogization and configurations section) to gradually emerge as an active area of exploration.
Solar reforming is the sunlight-driven transformation of waste substrates to valuable products (such as sustainable fuels and chemicals) as defined by scientists Subhajit Bhattacharjee, Stuart Linley and Erwin Reisner in their 2024 Nature Reviews Chemistry article where they conceptualized and formalized the field by introducing its concepts, classification, configurations and metrics. [1] It generally operates without external heating and pressure, and also introduces a thermodynamic advantage over traditional green hydrogen or CO2 reduction fuel producing methods such as water splitting or CO2 splitting, respectively. Depending on solar spectrum utilization, solar reforming can be classified into two categories: "solar catalytic reforming" and "solar thermal reforming". [1] Solar catalytic reforming refers to transformation processes primarily driven by ultraviolet (UV) or visible light. [1] It also includes the subset of 'photoreforming' encompassing utilization of high energy photons in the UV or near-UV region of the solar spectrum (for example, by semiconductor photocatalysts such as TiO2). Solar thermal reforming, on the other hand, exploits the infrared (IR) region for waste upcycling to generate products of high economic value. [1] An important aspect of solar reforming is value creation, which means that the overall value creation from product formation must be greater than substrate value destruction. [1] In terms of deployment architectures, solar catalytic reforming can be further categorized into: photocatalytic reforming (PC reforming), photoelectrochemical reforming (PEC reforming) and photovoltaic-electrochemical reforming (PV-EC reforming). [1]
Solar reforming offers several advantages over conventional methods of waste management or fuel/chemical production. It offers a less energy-intensive and low carbon alterative to methods of waste reforming such as pyrolysis and gasification which require high energy input. [1] Solar reforming also provides several benefits over traditional green hydrogen production methods such as water splitting (H2O → H2 + 1/2O2, ΔG° = 237 kJ mol−1). It offers a thermodynamic advantage over water splitting by circumventing the energetically and kinetically demanding water oxidation half reaction (E0 = +1.23 V vs. reversible hydrogen electrode (RHE)) by energetically neutral oxidation of waste-derived organics (CxHyOz + (2x−z)H2O → (2x−z+y/2)H2 + xCO2; ΔG° ~0 kJ mol−1). [1] This results in better performance in terms of higher production rates, and also translates to other similar processes which depend on water oxidation as the counter reaction such as CO2 splitting. Furthermore, concentrated streams of hydrogen produced from solar reforming is safer than explosive mixtures of oxygen and hydrogen (from traditional water splitting), that otherwise require additional separation costs. [1] The added economic advantage of forming two different valuable products (for example, gaseous reductive fuels and liquid oxidative chemicals) simultaneously makes solar reforming suitable for commercial applications. [1]
Solar reforming encompasses a range of technological processes and configurations and therefore, suitable performance metrics can evaluate the commercial viability. In artificial photosynthesis, the most common metric is the solar-to-fuel conversion efficiency (ηSTF) as shown below, where 'r' is the product formation rate, 'ΔG' is the Gibbs free energy change during the process, 'A' is the sunlight irradiation area and 'P' is the total light intensity flux. [1] [23] The ηSTF can be adopted as a metric for solar reforming but with certain considerations. Since the ΔG values for solar reforming processes are very low (ΔG ~0 kJ mol‒1), this makes the ηSTF per definition close to zero, despite the high production rates and quantum yields. However, replacing the ΔG for product formation (during solar reforming) with that of product utilisation (|ΔGuse|; such as combustion of the hydrogen fuel generated) can give a better representation of the process efficiency. [1]
Since solar reforming is highly dependent on the light harvester and its area of photon collection, a more technologically relevant metric is the areal production rate (rareal) as shown, where 'n' is the moles of product formed, 'A' is the sunlight irradiation area and 't' is the time. [1]
Although rareal is a more consistent metric for solar reforming, it neglects some key parameters such as type of waste utilized, pre-treatment costs, product value, scaling, other process and separation costs, deployment variables, etc. [1] Therefore, a more adaptable and robust metric is the solar-to-value creation rate (rSTV) which can encompass all these factors and provide a more holistic and practical picture from the economic or commercial point of view. [1] The simplified equation for rSTV is shown below, where Ci and Ck are the costs of the product 'i' and substrate 'k', respectively. Cp is the pre-treatment cost for the waste substrate 'k', and ni and nk are amounts (in moles) of the product 'i' formed and substrate 'k' consumed during solar reforming, respectively. Note that the metric is adaptable and can be expanded to include other relevant parameters as applicable. [1]
Solar reforming depends on the properties of the light absorber and the catalysts involved, and their selection, screening and integration to generate maximum value. The design and deployment of solar reforming technologies dictates the efficiency, scale and target substrates/products. In this context, solar reforming (more specifically, solar catalytic reforming) can be classified into three architectures: [1]
An important concept introduced in the context of solar reforming is the 'photon economy', which, as defined by Bhattacharjee, Linley and Reisner, is the maximum utilization of all incident photons for maximizing product formation and value creation. [1] An ideal solar reforming process is one where the light absorber can absorb incident UV and visible light photons with maximum quantum yield, generating high charge carrier concentration to drive redox half reactions at maximum rate. On the other hand, the residual, non-absorbed low-energy IR photons may be used for boosting reaction kinetics, waste pre-treatment or other means of value creation (for example, desalination, [34] etc.). Therefore, proper light and thermal management through various means (such as using solar concentrators, thermoelectric modules, among others) is encouraged to have both an atom economical and photon economical approach to extract maximum value from solar reforming processes.
The technological advancements in solar reforming garnered widespread interest in recent years. The works from scientists at Cambridge on PC reforming of raw lignocellulosic biomass or pre-treated polyester plastics to produce hydrogen and organics attracted attention of several stakeholders. [35] [36] [37] The recent technological breakthrough leading to the development of high-performing solar powered reactors (PEC reforming) for the simultaneous upcycling of greenhouse gas CO2 and waste plastics to sustainable products received widespread acclaim and was highlighted in several prominent national and international media outlets. [38] [39] [40] [41] [42] [43] [44] [45] [46] [47] [48] [49] [50] [51] [52] Solar reforming processes primarily developed in Cambridge were also selected as "one of the eleven great ideas from British universities that could change the world" by Sunday Times (April 2020 edition) [53] and featured in the UK Prime Minister's Speech on Net Zero, "Or the researchers at Cambridge who pioneered a new way to turn sunlight into fuel" [54] (indicating solar reforming which was a major subset of the broader research activities at Cambridge).
Solar reforming is currently in the development phase and the scalable deployment of a particular solar reforming technology (PC, PEC or PV-EC) would depend on a variety of factors. These factors include deployment location and sunlight variability/intermittency, characteristics of the chosen waste stream, viable pre-treatment methods, target products, nature of the catalysts and their lifetime, fuel/chemical storage requirements, land use versus open water sources, capital and operational costs, production and solar-to-value creation rates, and governmental policies and incentives, among others. [1] Solar reforming may not be only limited to the conventional chemical pathways discussed, and may also include other relevant industrial processes such as light-driven organic transformations, flow photochemistry, integration with industrial electrolysis, among others. [1] The products from conventional solar reforming such as green hydrogen or other platform chemicals have a broad value-chain. It is also now understood that sustainable fuel/chemical producing technologies of the future will rely on biomass, plastics and CO2 as key carbon feedstocks to replace fossil fuels. [55] Therefore, with sunlight being abundant and the cheapest source of energy, solar reforming is well-positioned to drive decarbonization and facilitate the transition from a linear to circular economy in the coming decades. [1]
Biofuel is a fuel that is produced over a short time span from biomass, rather than by the very slow natural processes involved in the formation of fossil fuels such as oil. Biofuel can be produced from plants or from agricultural, domestic or industrial biowaste. Biofuels are mostly used for transportation, but can also be used for heating and electricity. Biofuels are regarded as a renewable energy source. The use of biofuel has been subject to criticism regarding the "food vs fuel" debate, varied assessments of their sustainability, and possible deforestation and biodiversity loss as a result of biofuel production.
Syngas, or synthesis gas, is a mixture of hydrogen and carbon monoxide, in various ratios. The gas often contains some carbon dioxide and methane. It is principally used for producing ammonia or methanol. Syngas is combustible and can be used as a fuel. Historically, it has been used as a replacement for gasoline, when gasoline supply has been limited; for example, wood gas was used to power cars in Europe during WWII.
Thermal depolymerization (TDP) is the process of converting a polymer into a monomer or a mixture of monomers, by predominantly thermal means. It may be catalyzed or un-catalyzed and is distinct from other forms of depolymerization which may rely on the use of chemicals or biological action. This process is associated with an increase in entropy.
Pyrolysis is the process of thermal decomposition of materials at elevated temperatures, often in an inert atmosphere.
Gasification is a process that converts biomass- or fossil fuel-based carbonaceous materials into gases, including as the largest fractions: nitrogen (N2), carbon monoxide (CO), hydrogen (H2), and carbon dioxide (CO2). This is achieved by reacting the feedstock material at high temperatures (typically >700 °C), without combustion, via controlling the amount of oxygen and/or steam present in the reaction. The resulting gas mixture is called syngas (from synthesis gas) or producer gas and is itself a fuel due to the flammability of the H2 and CO of which the gas is largely composed. Power can be derived from the subsequent combustion of the resultant gas, and is considered to be a source of renewable energy if the gasified compounds were obtained from biomass feedstock.
Steam reforming or steam methane reforming (SMR) is a method for producing syngas (hydrogen and carbon monoxide) by reaction of hydrocarbons with water. Commonly natural gas is the feedstock. The main purpose of this technology is hydrogen production. The reaction is represented by this equilibrium:
Artificial photosynthesis is a chemical process that biomimics the natural process of photosynthesis. The term artificial photosynthesis is used loosely, referring to any scheme for capturing and then storing energy from sunlight by producing a fuel, specifically a solar fuel. An advantage of artificial photosynthesis would be that the solar energy could converted and stored. By contrast, using photovoltaic cells, sunlight is converted into electricity and then converted again into chemical energy for storage, with some necessary losses of energy associated with the second conversion. The byproducts of these reactions are environmentally friendly. Artificially photosynthesized fuel would be a carbon-neutral source of energy, but it has never been demonstrated in any practical sense. The economics of artificial photosynthesis are noncompetitive.
Water splitting is the chemical reaction in which water is broken down into oxygen and hydrogen:
In chemistry, photocatalysis is the acceleration of a photoreaction in the presence of a photocatalyst, the excited state of which "repeatedly interacts with the reaction partners forming reaction intermediates and regenerates itself after each cycle of such interactions." In many cases, the catalyst is a solid that upon irradiation with UV- or visible light generates electron–hole pairs that generate free radicals. Photocatalysts belong to three main groups; heterogeneous, homogeneous, and plasmonic antenna-reactor catalysts. The use of each catalysts depends on the preferred application and required catalysis reaction.
The methanol economy is a suggested future economy in which methanol and dimethyl ether replace fossil fuels as a means of energy storage, ground transportation fuel, and raw material for synthetic hydrocarbons and their products. It offers an alternative to the proposed hydrogen economy or ethanol economy, although these concepts are not exclusive. Methanol can be produced from a variety of sources including fossil fuels as well as agricultural products and municipal waste, wood and varied biomass. It can also be made from chemical recycling of carbon dioxide.
Waste-to-energy (WtE) or energy-from-waste (EfW) is the process of generating energy in the form of electricity and/or heat from the primary treatment of waste, or the processing of waste into a fuel source. WtE is a form of energy recovery. Most WtE processes generate electricity and/or heat directly through combustion, or produce a combustible fuel commodity, such as methane, methanol, ethanol or synthetic fuels, often derived from the product syngas.
Hydrogen gas is produced by several industrial methods. Nearly all of the world's current supply of hydrogen is created from fossil fuels. Most hydrogen is gray hydrogen made through steam methane reforming. In this process, hydrogen is produced from a chemical reaction between steam and methane, the main component of natural gas. Producing one tonne of hydrogen through this process emits 6.6–9.3 tonnes of carbon dioxide. When carbon capture and storage is used to remove a large fraction of these emissions, the product is known as blue hydrogen.
Biodegradable plastics are plastics that can be decomposed by the action of living organisms, usually microbes, into water, carbon dioxide, and biomass. Biodegradable plastics are commonly produced with renewable raw materials, micro-organisms, petrochemicals, or combinations of all three.
Renewable Fuels are fuels produced from renewable resources. Examples include: biofuels, Hydrogen fuel, and fully synthetic fuel produced from ambient carbon dioxide and water. This is in contrast to non-renewable fuels such as natural gas, LPG (propane), petroleum and other fossil fuels and nuclear energy. Renewable fuels can include fuels that are synthesized from renewable energy sources, such as wind and solar. Renewable fuels have gained in popularity due to their sustainability, low contributions to the carbon cycle, and in some cases lower amounts of greenhouse gases. The geo-political ramifications of these fuels are also of interest, particularly to industrialized economies which desire independence from Middle Eastern oil.
Photocatalytic water splitting is a process that uses photocatalysis for the dissociation of water (H2O) into hydrogen (H
2) and oxygen (O
2). The inputs are light energy (photons), water, and a catalyst(s). The process is inspired by Photosynthesis, which converts water and carbon dioxide into oxygen and carbohydrates. Water splitting using solar radiation has not been commercialized. Photocatalytic water splitting is done by dispersing photocatalyst particles in water or depositing them on a substrate, unlike Photoelectrochemical cell, which are assembled into a cell with a photoelectrode. Hydrogen fuel production using water and light (photocatalytic water splitting), instead of petroleum, is an important renewable energy strategy.
Photochemical reduction of carbon dioxide harnesses solar energy to convert CO2 into higher-energy products. Environmental interest in producing artificial systems is motivated by recognition that CO2 is a greenhouse gas. The process has not been commercialized.
Solar–hydrogen energy cycle is an energy cycle where a solar powered electrolyzer is used to convert water to hydrogen and oxygen. Hydrogen and oxygen produced thus are stored to be used by a fuel cell to produce electricity when no sunlight is available.
A solar fuel is a synthetic chemical fuel produced from solar energy. Solar fuels can be produced through photochemical, photobiological, and electrochemical reactions.
Vivek Vijayrao Polshettiwar is an Indian chemist who is a professor of chemistry at the Tata Institute of Fundamental Research. His research focuses on advanced nanomaterials and nanocatalysis, particularly for harvesting solar energy and converting carbon dioxide into valuable chemicals and fuels. He believes that the next generation of catalysts can be developed by fine-tuning the morphology of nanomaterials, defect engineering, metal-support interactions, and plasmonic properties. He aims to push the boundaries of catalytic research, ultimately creating nanocatalysts designed to harness solar energy, green hydrogen, and carbon dioxide. His work is aimed at producing value-added products to effectively combat climate change. He was awarded the International Union of Pure and Applied Chemistry prize for Green Chemistry in 2022. In 2023, he received the Falling Walls Award in Physical Sciences. The following year, in 2024, he was elected as a Fellow of the Indian Academy of Sciences (FASc).
Krishnan Rajeshwar is a chemist, researcher and academic. He is a Distinguished University Professor and Founding Director of the Center for Renewable Energy Science & Technology at The University of Texas at Arlington.