An official website of the United States government
Renewable energy-driven hydrogen production from electrocatalytic and photocatalytic water splitting has been widely recognized as a promising approach to utilize green energy resources and hence reduces our dependence on legacy fossil fuels as well as alleviates net carbon dioxide emissions. The realization of large-scale water splitting, however, is mainly impeded by its slow kinetics, particularly because of its sluggish anodic half reaction, the oxygen evolution reaction (OER), whose product O 2 is ironically not of high value. In fact, the co-production of H 2 and O 2 in conventional water electrolysis may result in the formation of explosive H 2 /O 2 gas mixtures due to gas crossover and reactive oxygen species (ROS); both pose safety concerns and shorten the lifetimes of water splitting cells. With these considerations in mind, replacing the OER with thermodynamically more favorable organic oxidation reactions is much more preferred, which will not only substantially reduce the voltage input for H 2 evolution from water and avoid the generation of H 2 /O 2 gas mixtures and ROS, but also possibly lead to the co-production of value-added organic products on the anode. Indeed, such an innovative strategy for H 2 production integrated with valuable organic oxidation has attracted increasing attention in both electrocatalysis and photocatalysis. This feature article showcases the most recent examples along this endeavor. As exemplified in the main text, the oxidative transformation of a variety of organic substrates, including alcohols, ammonia, urea, hydrazine, and biomass-derived intermediate chemicals, can be integrated with energy-efficient H 2 evolution. We specifically highlight the importance of oxidative biomass valorization coupled with H 2 production, as biomass is the only green carbon source whose scale is comparable to fossil fuels. Finally, the remaining challenges and future opportunities are also discussed.
more »
« less
This content will become publicly available on April 14, 2026
Biomass Valorization via Paired Electrocatalysis
Abstract Electrochemical valorization of biomass represents an emerging research frontier, capitalizing on renewable feedstocks to mitigate carbon emissions. Traditional electrochemical approaches often suffer from energy inefficiencies due to the requirement of a second electrochemical conversion at the counter electrode which might generate non‐value‐added byproducts. This review article presents the advancement of paired electrocatalysis as an alternative strategy, wherein both half‐reactions in an electrochemical cell are harnessed to concurrently produce value‐added chemicals from biomass‐derived feedstocks, potentially doubling the Faradaic efficiency of the whole process. The operational principles and advantages of different cell configurations, including 1‐compartment undivided cells, H‐type cells, and flow cells, in the context of paired electrolysis are introduced and compared, followed by the analysis of various catalytic strategies, from catalyst‐free systems to sophisticated homogeneous and heterogeneous electrocatalysts, tailored for optimized performance. Key substrates, such as CO2, 5‐hydroxymethylfurfural (HMF), furfural, glycerol, and lignin are highlighted to demonstrate the versatility and efficacy of paired electrocatalysis. This work aims to provide a clear understanding of why and how both cathode and anode reactions can be effectively utilized in electrocatalytic biomass valorization leading to innovative industrial scalability.
more »
« less
- PAR ID:
- 10653469
- Publisher / Repository:
- Wiley-VCH GmbH
- Date Published:
- Journal Name:
- ChemSusChem
- Volume:
- 18
- Issue:
- 8
- ISSN:
- 1864-5631
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
-
Electrocatalytic upgrading of biomass-derived feedstocks driven by renewable electricity offers a greener way to reduce the global carbon footprint associated with the production of value-added chemicals. Paired electrolysis is an emerging platform for cogenerating high-valued chemicals from both the cathode and anode, potentially powered by renewable electricity from wind or solar sources. By pairing with an anodic biomass oxidation upgrading reaction, the elimination of the sluggish and less valuable water oxidation increases flow cell productivity and efficiency. In this presentation, we report our research progress on paired electrolsysis of HMF to production of higher valued chemicals in electrochemical flow cells. We first prepared an oxide-derived Ag (OD-Ag) electrode with high activity and up to 98.2% selectivity for the ECH of 5-(hydroxymethyl)furfural (HMF) to 2,5-bis(hydroxymethyl)furan (BHMF), and such efficient conversion was achieved in a three-electrode flow cell. The excellent BHMF selectivity was maintained over a broad potential range with long-term operational stability. In HMF-to-BHMF paired with 2,2,6,6-tetramethylpiperidine 1-oxyl (TEMPO)-mediated HMF-to-FDCA conversion, a markedly reduced cell voltage from ~7.5 V to ~2.0 V was observed by transferring the electrolysis from the H-type cell to the flow cell, corresponding to more than four-fold increase in energy efficiency in operation at 10 mA. A combined faradaic efficiency of 163% was obtained to BHMF and FDCA. Alternatively, the anodic hydrogen oxidation reaction on platinum further reduced the cell voltage to only ~0.85 V at 10 mA. Next, we have demonstrated membrane electrode assembly (MEA)-based flow cells for the paired electrolysis of 5-(hydroxymethyl)furfural (HMF) paired electrolysis to bis(hydroxymethyl)furan (BHMF) and 2,5-furandicarboxylic acid (FDCA). In this work, the oxygen evolution reaction (OER) was substituted by TEMPO-mediated HMF oxidation, dropping the cell voltage was from 1.4 V to 0.7 V at a current density of 1.0 mA cm−2. A minimized cell voltage of ~1.5 V for a continuous 24 h co-electrolysis of HMF was then achieved at the current density of 2 mA cm−2(constant current of 10 mA), leading to the highest combined faradaic efficiency (FE) of 139% for HMF-to-BHMF and HMF-to-FDCA. A NiFe oxide catalyst on carbon cloth further replaced the anodic TEMPO mediator for HMF paired electrolysis in a pH-asymmetric flow cell. We envision renewable electrical energy can potentially drive the whole process, thus providing a sustainable avenue towards distributed, scalable, and energy-efficient electrosynthesis.more » « less
-
Abstract Bioelectrocatalytic synthesis is the conversion of electrical energy into value‐added products using biocatalysts. These methods merge the specificity and selectivity of biocatalysis and energy‐related electrocatalysis to address challenges in the sustainable synthesis of pharmaceuticals, commodity chemicals, fuels, feedstocks and fertilizers. However, the specialized experimental setups and domain knowledge for bioelectrocatalysis pose a significant barrier to adoption. This review introduces key concepts of bioelectrosynthetic systems. We provide a tutorial on the methods of biocatalyst utilization, the setup of bioelectrosynthetic cells, and the analytical methods for assessing bioelectrocatalysts. Key applications of bioelectrosynthesis in ammonia production and small‐molecule synthesis are outlined for both enzymatic and microbial systems. This review serves as a necessary introduction and resource for the non‐specialist interested in bioelectrosynthetic research.more » « less
-
null (Ed.)Due to its clean and sustainable nature, solar energy has been widely recognized as a green energy source in driving a variety of reactions, ranging from small molecule activation and organic transformation to biomass valorization. Within this context, organic reactions coupled with H 2 evolution via semiconductor-based photocatalytic systems under visible light irradiation have gained increasing attention in recent years, which utilize both excited electrons and holes generated on semiconductors and produce two types of value-added products, organics and H 2 , simultaneously. Based on the nature of the organic reactions, in this review article we classify semiconductor-based photocatalytic organic transformations and H 2 evolution into three categories: (i) photocatalytic organic oxidation reactions coupled with H 2 production, including oxidative upgrading of alcohols and biomass-derived intermediate compounds; (ii) photocatalytic oxidative coupling reactions integrated with H 2 generation, such as C–C, C–N, and S–S coupling reactions; and (iii) photo-reforming reactions together with H 2 formation using organic plastics, pollutants, and biomass as the substrates. Representative heterogeneous photocatalytic systems will be highlighted. Specific emphasis will be placed on their synthesis, characterization, and photocatalytic mechanism, as well as the organic reaction scope and practical application.more » « less
-
null (Ed.)Electrocatalytic upgrading of biomass-derived feedstocks driven by renewable electricity offers a greener way to reduce the global carbon footprint associated with the production of value-added chemicals. In this respect, a key strategy is the electrocatalytic hydrogenation (ECH) reaction, which is typically paired with the anodic oxygen evolution reaction (OER) with sluggish kinetics, producing O 2 with little value. Here we prepared an oxide-derived Ag (OD-Ag) electrode with high activity and up to 98.2% selectivity for the ECH of 5-(hydroxymethyl)furfural (HMF) to 2,5-bis(hydroxymethyl)furan (BHMF), and such efficient conversion was achieved in a three-electrode flow cell. The excellent BHMF selectivity was maintained over a broad potential range with long-term operational stability. We then considered the oxidation of HMF to 2,5-furandicarboxylic acid (FDCA) and hydrogen (to water) as more efficient and productive alternatives to the OER. In HMF-to-BHMF paired with 2,2,6,6-tetramethylpiperidine 1-oxyl (TEMPO)-mediated HMF-to-FDCA conversion, a markedly reduced cell voltage from ∼7.5 V to ∼2.0 V was observed by transferring the electrolysis from the H-type cell to the flow cell, corresponding to more than four-fold increase in energy efficiency in operation at 10 mA. A combined faradaic efficiency of 163% was obtained for BHMF and FDCA. Alternatively, the anodic hydrogen oxidation reaction on platinum further reduced the cell voltage to only ∼0.85 V at 10 mA. These paired processes show the potential for integration of renewable electricity and carbon for green and economically feasible distributed chemical manufacturing.more » « less
