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Radical generation and fate control for photocatalytic biomass conversion

Abstract

Photocatalysis is an emerging approach for sustainable chemical production from renewable biomass under mild conditions. Active radicals are always generated as key intermediates, in which their high reactivity renders them versatile for various upgrading processes. However, controlling their reaction is a challenge, especially in highly functionalized biomass frameworks. In this Review, we summarize recent advanced photocatalytic systems for selective biomass valorization, with an emphasis on their distinct radical-mediated reaction patterns. The strategies for generating a specific radical intermediate and controlling its subsequent conversion towards desired chemicals are also highlighted, aiming to provide guidance for future studies. We believe that taking full advantage of the unique reactivity of radical intermediates would provide great opportunities to develop more efficient photocatalytic systems for biomass valorization.

Key points

  • Photocatalysis is an efficient approach for value-added chemical production from renewable biomass under mild conditions.

  • The active and energetic nature of light-induced radical intermediates offers unique reaction patterns for selective biomass valorization, but efficient strategies for manipulating their generation and subsequent conversion are needed.

  • The formation of a specific radical intermediate from biomass substrates is the prerequisite for selective biomass upgrading by photocatalysis, which relies greatly on the rational design of catalytic systems.

  • The introduction of suitable extraneous radical species is an alternative solution to achieve challenging transformations.

  • Subtly tuning the interactions between catalyst and light-induced radical species is imperative to modulate the conversion of radical intermediates towards desired products.

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Fig. 1: Schematic representation of chemical production from renewable biomass via radical-mediated photocatalytic pathways.
Fig. 2: Strategies for preferential activation of O–H bond and Cα–Cβ bond cleavage in lignin β-O-4 and β-1 linkages.
Fig. 3: CeCl3-promoted photocatalytic Cα–Cβ bond cleavage in lignin β-O-4 linkage via LMCT process.
Fig. 4: Carbon-radical-mediated oxidative lignin C–C bond cleavage.
Fig. 5: Cation-radical-induced bond cleavage in dimeric, tetrameric and pre-oxidized lignin models.
Fig. 6: Photocatalytic conversion of furfural over TiO2.
Fig. 7: Active external radical species induce lignin bond cleavage.
Fig. 8: Regulating the conversion of radical intermediates derived from lignin, polyol molecules and fatty acids.

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References

  1. Liao, Y. et al. A sustainable wood biorefinery for low-carbon footprint chemicals production. Science 367, 1385–1390 (2020).

    Article  CAS  PubMed  Google Scholar 

  2. Amidon, T. E. & Liu, S. Water-based woody biorefinery. Biotechnol. Adv. 27, 542–550 (2009).

    Article  CAS  PubMed  Google Scholar 

  3. Deneyer, A. et al. Direct upstream integration of biogasoline production into current light straight run naphtha petrorefinery processes. Nat. Energy 3, 969–977 (2018).

    Article  CAS  Google Scholar 

  4. Li, C., Zhao, X., Wang, A., Huber, G. W. & Zhang, T. Catalytic transformation of lignin for the production of chemicals and fuels. Chem. Rev. 115, 11559–11624 (2015).

    Article  CAS  PubMed  Google Scholar 

  5. Granone, L. I., Sieland, F., Zheng, N., Dillert, R. & Bahnemann, D. W. Photocatalytic conversion of biomass into valuable products: a meaningful approach? Green Chem. 20, 1169–1192 (2018).

    Article  CAS  Google Scholar 

  6. Liu, X., Duan, X., Wei, W., Wang, S. & Ni, B.-J. Photocatalytic conversion of lignocellulosic biomass to valuable products. Green Chem. 21, 4266–4289 (2019).

    Article  CAS  Google Scholar 

  7. Wu, X. et al. Photocatalytic transformations of lignocellulosic biomass into chemicals. Chem. Soc. Rev. 49, 6198–6223 (2020). This is an up-to-date and comprehensive review on photocatalytic conversion of lignocellulosic biomass.

    Article  CAS  PubMed  Google Scholar 

  8. Luo, N. et al. Visible-light-driven coproduction of diesel precursors and hydrogen from lignocellulose-derived methylfurans. Nat. Energy 4, 575–584 (2019).

    Article  CAS  Google Scholar 

  9. Zhang, C. & Wang, F. Catalytic lignin depolymerization to aromatic chemicals. Acc. Chem. Res. 53, 470–484 (2020).

    Article  CAS  PubMed  Google Scholar 

  10. Recupero, F. & Punta, C. Free radical functionalization of organic compounds catalyzed by N-hydroxyphthalimide. Chem. Rev. 107, 3800–3842 (2007).

    Article  CAS  PubMed  Google Scholar 

  11. Wu, X. et al. Selectivity control in photocatalytic valorization of biomass-derived platform compounds by surface engineering of titanium oxide. Chem 6, 3038–3053 (2020). This paper shows that regulating the interactions between substrate and catalyst by surface engineering can selectively activate furfural into an oxygen or carbon radical intermediate.

    Article  CAS  Google Scholar 

  12. Yi, H. et al. Recent advances in radical C–H activation/radical cross-coupling. Chem. Rev. 117, 9016–9085 (2017).

    Article  CAS  PubMed  Google Scholar 

  13. Xie, J., Jin, H. & Hashmi, A. S. K. The recent achievements of redox-neutral radical C–C cross-coupling enabled by visible-light. Chem. Soc. Rev. 46, 5193–5203 (2017).

    Article  CAS  PubMed  Google Scholar 

  14. Gao, Z., Luo, N., Huang, Z., Taylor, S. H. & Wang, F. Controlling radical intermediates in photocatalytic conversion of low-carbon-number alcohols. ACS Sustain. Chem. Eng. 9, 6188–6202 (2021).

    Article  CAS  Google Scholar 

  15. Yayla, H. G., Wang, H., Tarantino, K. T., Orbe, H. S. & Knowles, R. R. Catalytic ring-opening of cyclic alcohols enabled by PCET activation of strong O–H bonds. J. Am. Chem. Soc. 138, 10794–10797 (2016).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  16. Ota, E., Wang, H., Frye, N. L. & Knowles, R. R. A redox strategy for light-driven, out-of-equilibrium isomerizations and application to catalytic C–C bond cleavage reactions. J. Am. Chem. Soc. 141, 1457–1462 (2019).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  17. Wu, X. et al. Solar energy-driven lignin-first approach to full utilization of lignocellulosic biomass under mild conditions. Nat. Catal. 1, 772–780 (2018). This paper reports a photoredox electron–hole coupled protocol for lignin β-O-4 bond cleavage.

    Article  CAS  Google Scholar 

  18. Wang, Y., Liu, Y., He, J. & Zhang, Y. Redox-neutral photocatalytic strategy for selective C–C bond cleavage of lignin and lignin models via PCET process. Sci. Bull. 64, 1658–1666 (2019).

    Article  CAS  Google Scholar 

  19. Mayer, J. M., Hrovat, D. A., Thomas, J. L. & Borden, W. T. Proton-coupled electron transfer versus hydrogen atom transfer in benzyl/toluene, methoxyl/methanol, and phenoxyl/phenol self-exchange reactions. J. Am. Chem. Soc. 124, 11142–11147 (2002).

    Article  CAS  PubMed  Google Scholar 

  20. Nguyen, S. T., Murray, P. R. D. & Knowles, R. R. Light-driven depolymerization of native lignin enabled by proton-coupled electron transfer. ACS Catal. 10, 800–805 (2020).

    Article  CAS  Google Scholar 

  21. Zhou, W., Nakahashi, J., Miura, T. & Murakami, M. Light/copper relay for aerobic fragmentation of lignin model compounds. Asian J. Org. Chem. 7, 2431–2434 (2018).

    Article  CAS  Google Scholar 

  22. Gazi, S. et al. Selective photocatalytic C–C bond cleavage under ambient conditions with earth abundant vanadium complexes. Chem. Sci. 6, 7130–7142 (2015).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  23. Gazi, S. et al. Kinetics and DFT studies of photoredox carbon–carbon bond cleavage reactions by molecular vanadium catalysts under ambient conditions. ACS Catal. 7, 4682–4691 (2017).

    Article  CAS  Google Scholar 

  24. Liu, H., Li, H., Luo, N. & Wang, F. Visible-light-induced oxidative lignin C–C bond cleavage to aldehydes using vanadium catalysts. ACS Catal. 10, 632–643 (2020).

    Article  CAS  Google Scholar 

  25. Wang, Y., He, J. & Zhang, Y. CeCl3-promoted simultaneous photocatalytic cleavage and amination of Cα–Cβ bond in lignin model compounds and native lignin. CCS Chem. 2, 107–117 (2020).

    Article  CAS  Google Scholar 

  26. Hou, T. et al. Yin and Yang dual characters of CuOx clusters for C–C bond oxidation driven by visible light. ACS Catal. 7, 3850–3859 (2017).

    Article  CAS  Google Scholar 

  27. Zhao, K. et al. Efficient water oxidation under visible light by tuning surface defects on ceria nanorods. J. Mater. Chem. A 3, 20465–20470 (2015).

    Article  CAS  Google Scholar 

  28. Liu, H. et al. Photocatalytic cleavage of C–C bond in lignin models under visible light on mesoporous graphitic carbon nitride through π–π stacking interaction. ACS Catal. 8, 4761–4771 (2018).

    Article  CAS  Google Scholar 

  29. Kang, Y. et al. Metal-free photochemical degradation of lignin-derived aryl ethers and lignin by autologous radicals through ionic liquid induction. ChemSusChem 12, 4005–4013 (2019).

    Article  CAS  PubMed  Google Scholar 

  30. Wang, M. et al. Acid promoted C–C bond oxidative cleavage of β-O-4 and β-1 lignin models to esters over a copper catalyst. Green Chem. 19, 702–706 (2017).

    Article  CAS  Google Scholar 

  31. Ma, L., Zhou, H., Kong, X., Li, Z. & Duan, H. An electrocatalytic strategy for C–C bond cleavage in lignin model compounds and lignin under ambient conditions. ACS Sustain. Chem. Eng. 9, 1932–1940 (2021).

    Article  CAS  Google Scholar 

  32. Cui, T. et al. Atomically dispersed Pt–N3C1 sites enabling efficient and selective electrocatalytic C–C bond cleavage in lignin models under ambient conditions. J. Am. Chem. Soc. 143, 9429–9439 (2021).

    Article  CAS  PubMed  Google Scholar 

  33. Have, R. T. & Teunissen, P. J. M. Oxidative mechanisms involved in lignin degradation by white-rot fungi. Chem. Rev. 101, 3397–3413 (2001).

    Article  PubMed  Google Scholar 

  34. Cho, D. W. et al. Nature and kinetic analysis of carbon–carbon bond fragmentation reactions of cation radicals derived from SET-oxidation of lignin model compounds. J. Org. Chem. 75, 6549–6562 (2010).

    Article  CAS  PubMed  Google Scholar 

  35. Cho, D. W. et al. Regioselectivity of enzymatic and photochemical single electron transfer promoted carbon–carbon bond fragmentation reactions of tetrameric lignin model compounds. J. Org. Chem. 76, 2840–2852 (2011).

    Article  CAS  PubMed  Google Scholar 

  36. Lim, S. H. et al. Effects of alkoxy groups on arene rings of lignin β-O-4 model compounds on the efficiencies of single electron transfer-promoted photochemical and enzymatic C–C bond cleavage reactions. J. Org. Chem. 78, 9431–9443 (2013).

    Article  CAS  PubMed  Google Scholar 

  37. Tay, N. E. S. & Nicewicz, D. A. Cation radical accelerated nucleophilic aromatic substitution via organic photoredox catalysis. J. Am. Chem. Soc. 139, 16100–16104 (2017).

    Article  CAS  PubMed  Google Scholar 

  38. Werpy, T. & Petersen, G. Top value added chemicals from biomass. Volume I — Results of screening for potential candidates from sugars and synthesis gas (US Department of Energy, 2004).

  39. Bozell, J. J. & Petersen, G. R. Technology development for the production of biobased products from biorefinery carbohydrates — the US Department of Energy’s “Top 10” revisited. Green Chem. 12, 539–554 (2010).

    Article  CAS  Google Scholar 

  40. Mika, L. T., Cséfalvay, E. & Németh, Á. Catalytic conversion of carbohydrates to initial platform chemicals: chemistry and sustainability. Chem. Rev. 118, 505–613 (2017).

    Article  PubMed  Google Scholar 

  41. Shylesh, S., Gokhale, A. A., Ho, C. R. & Bell, A. T. Novel strategies for the production of fuels, lubricants, and chemicals from biomass. Acc. Chem. Res. 50, 2589–2597 (2017).

    Article  CAS  PubMed  Google Scholar 

  42. Nakajima, M., Fava, E., Loescher, S., Jiang, Z. & Rueping, M. Photoredox-catalyzed reductive coupling of aldehydes, ketones, and imines with visible light. Angew. Chem. Int. Ed. 54, 8828–8832 (2015).

    Article  CAS  Google Scholar 

  43. Han, G., Liu, X., Cao, Z. & Sun, Y. Photocatalytic pinacol C–C coupling and jet fuel precursor production on ZnIn2S4 nanosheets. ACS Catal. 10, 9346–9355 (2020).

    Article  CAS  Google Scholar 

  44. Sun, Z., Fridrich, B., de Santi, A., Elangovan, S. & Barta, K. Bright side of lignin depolymerization: toward new platform chemicals. Chem. Rev. 118, 614–678 (2018).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  45. Tan, F.-F., He, X.-Y., Tian, W.-F. & Li, Y. Visible-light photoredox-catalyzed C–O bond cleavage of diaryl ethers by acridinium photocatalysts at room temperature. Nat. Commun. 11, 6126 (2020). This paper reports a strategy to use extraneous radical species to cleave C–O bonds in diaryl ethers.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  46. Zeng, H., Cao, D., Qiu, Z. & Li, C.-J. Palladium-catalyzed formal cross-coupling of diaryl ethers with amines: slicing the 4-O-5 linkage in lignin models. Angew. Chem. Int. Ed. 57, 3752–3757 (2018).

    Article  CAS  Google Scholar 

  47. Li, H., Bunrit, A., Li, N. & Wang, F. Heteroatom-participated lignin cleavage to functionalized aromatics. Chem. Soc. Rev. 49, 3748–3763 (2020).

    Article  CAS  PubMed  Google Scholar 

  48. Li, H. et al. Photocatalytic cleavage of aryl ether in modified lignin to non-phenolic aromatics. ACS Catal. 9, 8843–8851 (2019).

    Article  CAS  Google Scholar 

  49. Zhang, C. & Wang, F. Sell a dummy: adjacent functional group modification strategy for the catalytic cleavage of lignin β-O-4 linkage. Chin. J. Catal. 38, 1102–1107 (2017).

    Article  CAS  Google Scholar 

  50. Nguyen, J. D., Matsuura, B. S. & Stephenson, C. R. J. A photochemical strategy for lignin degradation at room temperature. J. Am. Chem. Soc. 136, 1218–1221 (2014).

    Article  CAS  PubMed  Google Scholar 

  51. Magallanes, G. et al. Selective C–O bond cleavage of lignin systems and polymers enabled by sequential palladium-catalyzed aerobic oxidation and visible-light photoredox catalysis. ACS Catal. 9, 2252–2260 (2019).

    Article  CAS  Google Scholar 

  52. Yang, C., Kärkäs, M. D., Magallanes, G., Chan, K. & Stephenson, C. R. J. Organocatalytic approach to photochemical lignin fragmentation. Org. Lett. 22, 8082–8085 (2020).

    Article  CAS  PubMed  Google Scholar 

  53. Luo, N. et al. Photocatalytic oxidation–hydrogenolysis of lignin β-O-4 models via a dual light wavelength switching strategy. ACS Catal. 6, 7716–7721 (2016).

    Article  CAS  Google Scholar 

  54. Luo, J., Zhang, X., Lu, J. & Zhang, J. Fine tuning the redox potentials of carbazolic porous organic frameworks for visible-light photoredox catalytic degradation of lignin β-O-4 models. ACS Catal. 7, 5062–5070 (2017).

    Article  CAS  Google Scholar 

  55. Luo, N. et al. Visible-light-driven self-hydrogen transfer hydrogenolysis of lignin models and extracts into phenolic products. ACS Catal. 7, 4571–4580 (2017).

    Article  CAS  Google Scholar 

  56. Han, G. et al. Highly selective photocatalytic valorization of lignin model compounds using ultrathin metal/CdS. ACS Catal. 9, 11341–11349 (2019).

    Article  CAS  Google Scholar 

  57. Chen, K., Schwarz, J., Karl, T. A., Chatterjee, A. & König, B. Visible light induced redox neutral fragmentation of 1,2-diol derivatives. Chem. Commun. 55, 13144–13147 (2019).

    Article  CAS  Google Scholar 

  58. Wu, X. et al. Ligand-controlled photocatalysis of CdS quantum dots for lignin valorization under visible light. ACS Catal. 9, 8443–8451 (2019).

    Article  CAS  Google Scholar 

  59. Yoo, H. et al. Enhancing photocatalytic β-O-4 bond cleavage in lignin model compounds by silver-exchanged cadmium sulfide. ACS Catal. 10, 8465–8475 (2020).

    Article  CAS  Google Scholar 

  60. Lin, J. et al. Visible-light-driven cleavage of C–O linkage for lignin valorization to functionalized aromatics. ChemSusChem 12, 5023–5031 (2019).

    Article  CAS  PubMed  Google Scholar 

  61. Zhang, C. et al. Cleavage of the lignin β-O-4 ether bond via a dehydroxylation–hydrogenation strategy over a NiMo sulfide catalyst. Green Chem. 18, 6545–6555 (2016).

    Article  CAS  Google Scholar 

  62. Pagliaro, M., Ciriminna, R., Kimura, H., Rossi, M. & Della Pina, C. From glycerol to value-added products. Angew. Chem. Int. Ed. 46, 4434–4440 (2007).

    Article  CAS  Google Scholar 

  63. Yang, F., Hanna, M. A. & Sun, R. Value-added uses for crude glycerol–a byproduct of biodeisel production. Biotechnol. Biofuels 5, 13 (2012).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  64. Shimura, K. & Yoshida, H. Heterogeneous photocatalytic hydrogen production from water and biomass derivatives. Energy Environ. Sci. 4, 2467–2481 (2011).

    Article  CAS  Google Scholar 

  65. Kawai, T. & Sakata, T. Conversion of carbohydrate into hydrogen fuel by a photocatalytic process. Nature 286, 474–476 (1980).

    Article  CAS  Google Scholar 

  66. Schneider, J. et al. Understanding TiO2 photocatalysis: mechanisms and materials. Chem. Rev. 114, 9919–9986 (2014).

    Article  CAS  PubMed  Google Scholar 

  67. Puga, A. V. Photocatalytic production of hydrogen from biomass-derived feedstocks. Coord. Chem. Rev. 315, 1–66 (2016).

    Article  CAS  Google Scholar 

  68. Kuehnel, M. F. & Reisner, E. Solar hydrogen generation from lignocellulose. Angew. Chem. Int. Ed. 57, 3290–3296 (2018).

    Article  CAS  Google Scholar 

  69. Wakerley, D. W. et al. Solar-driven reforming of lignocellulose to H2 with a CdS/CdOx photocatalyst. Nat. Energy 2, 17021 (2017).

    Article  CAS  Google Scholar 

  70. Jin, B., Yao, G., Wang, X., Ding, K. & Jin, F. Photocatalytic oxidation of glucose into formate on nano TiO2 catalyst. ACS Sustain. Chem. Eng. 5, 6377–6381 (2017).

    Article  CAS  Google Scholar 

  71. Chong, R. et al. Selective conversion of aqueous glucose to value-added sugar aldose on TiO2-based photocatalysts. J. Catal. 314, 101–108 (2014).

    Article  CAS  Google Scholar 

  72. Da Vià, L., Recchi, C., Gonzalez-Yañez, E. O., Davies, T. E. & Lopez-Sanchez, J. A. Visible light selective photocatalytic conversion of glucose by TiO2. Appl. Catal. B 202, 281–288 (2017).

    Article  Google Scholar 

  73. Li, Z., Kay, B. D. & Dohnálek, Z. Dehydration and dehydrogenation of ethylene glycol on rutile TiO2(110). Phys. Chem. Chem. Phys. 15, 12180–12186 (2013).

    Article  CAS  PubMed  Google Scholar 

  74. Kisch, H. Semiconductor photocatalysis for chemoselective radical coupling reactions. Acc. Chem. Res. 50, 1002–1010 (2017).

    Article  CAS  PubMed  Google Scholar 

  75. Schneider, J. & Bahnemann, D. W. Undesired role of sacrificial reagents in photocatalysis. J. Phys. Chem. Lett. 4, 3479–3483 (2013).

    Article  CAS  Google Scholar 

  76. Shkrob, I. A. & Wan, J. K. S. Chemically induced dynamic electron polarization (CIDEP) spectroscopy of radicals generated in the photoreactions of polyols: the mechanisms of radical dehydration. Res. Chem. Intermed. 18, 19–47 (1992).

    Article  CAS  Google Scholar 

  77. Shkrob, I. A., Myran, C. S. J. & Gosztola, D. Efficient, rapid photooxidation of chemisorbed polyhydroxyl alcohols and carbohydrates by TiO2 nanoparticles in an aqueous solution. J. Phys. Chem. B 108, 12512–12517 (2004).

    Article  CAS  Google Scholar 

  78. Copeland, J. R., Santillan, I. A., Schimming, S. M., Ewbank, J. L. & Sievers, C. Surface interactions of glycerol with acidic and basic metal oxides. J. Phys. Chem. C 117, 21413–21425 (2013).

    Article  CAS  Google Scholar 

  79. Jin, X. et al. Photocatalytic C–C bond cleavage in ethylene glycol on TiO2: a molecular level picture and the effect of metal nanoparticles. J. Catal. 354, 37–45 (2017).

    Article  CAS  Google Scholar 

  80. Balducci, G. The adsorption of glucose at the surface of anatase: a computational study. Chem. Phys. Lett. 494, 54–59 (2010).

    Article  CAS  Google Scholar 

  81. Shkrob, I. A., Marin, T. W., Chemerisov, S. D. & Sevilla, M. D. Mechanistic aspects of photooxidation of polyhydroxylated molecules on metal oxides. J. Phys. Chem. C 115, 4642–4648 (2011).

    Article  CAS  Google Scholar 

  82. Sanwald, K. E., Berto, T. F., Eisenreich, W., Gutiérrez, O. Y. & Lercher, J. A. Catalytic routes and oxidation mechanisms in photoreforming of polyols. J. Catal. 344, 806–816 (2016).

    Article  CAS  Google Scholar 

  83. Wang, M., Liu, M., Lu, J. & Wang, F. Photo splitting of bio-polyols and sugars to methanol and syngas. Nat. Commun. 11, 1083 (2020).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  84. Zhang, Z., Wang, M., Zhou, H. & Wang, F. Surface sulfate ion on CdS catalyst enhances syngas generation from biopolyols. J. Am. Chem. Soc. 143, 6533–6541 (2021). This paper shows that bio-polyols can be transfromed to CO via sequential acyl-radical-mediated decarbonylation processes.

    Article  CAS  PubMed  Google Scholar 

  85. Pattanaik, B. P. & Misra, R. D. Effect of reaction pathway and operating parameters on the deoxygenation of vegetable oils to produce diesel range hydrocarbon fuels: a review. Renew. Sustain. Energy Rev. 73, 545–557 (2017).

    Article  CAS  Google Scholar 

  86. Gosselink, R. W. et al. Reaction pathways for the deoxygenation of vegetable oils and related model compounds. ChemSusChem 6, 1576–1594 (2013).

    Article  CAS  PubMed  Google Scholar 

  87. Schwarz, J. & König, B. Decarboxylative reactions with and without light–a comparison. Green Chem. 20, 323–361 (2018).

    Article  CAS  Google Scholar 

  88. Manley, D. W. et al. Unconventional titania photocatalysis: direct deployment of carboxylic acids in alkylations and annulations. J. Am. Chem. Soc. 134, 13580–13583 (2012).

    Article  CAS  PubMed  Google Scholar 

  89. Manley, D. W. & Walton, J. C. A clean and selective radical homocoupling employing carboxylic acids with titania photoredox catalysis. Org. Lett. 16, 5394–5397 (2014).

    Article  CAS  PubMed  Google Scholar 

  90. Creusen, G., Holzhäuser, F. J., Artz, J., Palkovits, S. & Palkovits, R. Producing widespread monomers from biomass using economical carbon and ruthenium–titanium dioxide electrocatalysts. ACS Sustain. Chem. Eng. 6, 17108–17113 (2018).

    Article  CAS  Google Scholar 

  91. Huang, Z. et al. Enhanced photocatalytic alkane production from fatty acid decarboxylation via inhibition of radical oligomerization. Nat. Catal. 3, 170–178 (2020). This paper shows that alkane can be selectively produced from fatty acid decarboxylation via rapid radical hydrogenation over a hydrogen-rich catalyst surface.

    Article  CAS  Google Scholar 

  92. Bahnemann, W., Muneer, M. & Haque, M. M. Titanium dioxide-mediated photocatalysed degradation of few selected organic pollutants in aqueous suspensions. Catal. Today 124, 133–148 (2007).

    Article  CAS  Google Scholar 

  93. Liao, Y. et al. The role of pretreatment in the catalytic valorization of cellulose. Mol. Catal. 487, 110883 (2020).

    Article  CAS  Google Scholar 

  94. Rinaldi, R. et al. Paving the way for lignin valorisation: recent advances in bioengineering, biorefining and catalysis. Angew. Chem. Int. Ed. 55, 8164–8215 (2016).

    Article  CAS  Google Scholar 

  95. Abu-Omar, M. M. et al. Guidelines for performing lignin-first biorefining. Energy Environ. Sci. 14, 262–292 (2021).

    Article  Google Scholar 

  96. Herron, J. A., Kim, J., Upadhye, A. A., Huber, G. W. & Maravelias, C. T. A general framework for the assessment of solar fuel technologies. Energy Environ. Sci. 8, 126–157 (2015).

    Article  CAS  Google Scholar 

  97. Davis, R. et al. Process design and economics for the conversion of lignocellulosic biomass to hydrocarbon fuels and coproducts: 2018 biochemical design case update (NREL, 2018).

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Acknowledgements

The authors are grateful for financial support from the National Natural Science Foundation of China (22025206, 21991094, 21721004, 21690080), the Ministry of Science and Technology of the People’s Republic of China (2018YFE0117300), the CAS-NSTDA Joint Research Project (GJHZ2075), Dalian Science and Technology Innovation Fund (2019J11CY009) and Dalian Institute of Chemical Physics (DICP I202009).

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Glossary

Photo-generated carriers

Electronic carriers (including negatively charged electrons and positively charged holes) generated from light-excited semiconductors. When a photon with energy larger than the bandgap energy is absorbed by the semiconductor, an electron is excited into the conduction band, while creating a hole in the valence band.

Back electron transfer

Refers to the deactivation/quenching process of the activated substrate by charged species. After stimulation by a positively charged hole, for example, the activated substrate reacts with electron or hydrogen species and subsequently reforms to its initial state.

Density of states

A physical concept to describe the proportion of states that are to be occupied by the system at each energy level.

Photo-generated holes

Positively charged species generated from light-excited semiconductors.

Hole-trapping centres

Refers to the catalyst sites that can trap free photo-generated holes.

Oxidation by holes

(Also known as hole-induced oxidation). Oxidation reaction triggered by photo-generated holes.

Mott–Schottky junction

Refers to the metal–semiconductor junction that possesses an in-built potential energy barrier (Schottky barrier). This barrier allows electrons to transfer from the semiconductor to the metal but blocks the transfer process in the opposite direction.

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Huang, Z., Luo, N., Zhang, C. et al. Radical generation and fate control for photocatalytic biomass conversion. Nat Rev Chem 6, 197–214 (2022). https://doi.org/10.1038/s41570-022-00359-9

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