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Cited by 67Advanced Photocatalysis TechniquesCatalysis for Biomass ConversionThermochemical Biomass Conversion Processes

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Solar‐Driven Biomass Reforming for Hydrogen Generation: Principles, Advances, and Challenges

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Pan, Hu, Li, Jinglin, Wang, Yangang, Xia, Qineng, Qiu, Liang, Zhou, Baowen·2024·Advanced Science
DOI 10.1002/advs.202402651PMC PMC11304308
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Abstract

Hydrogen (H 2) has emerged as a clean and versatile energy carrier to power a carbon‐neutral economy for the post‐fossil era. Hydrogen generation from low‐cost and renewable biomass by virtually inexhaustible solar energy presents an innovative strategy to process organic solid waste, combat the energy crisis, and achieve carbon neutrality. Herein, the progress and breakthroughs in solar‐powered H 2 production from biomass are reviewed. The basic principles of solar‐driven H 2 generation from biomass are first introduced for a better understanding of the reaction mechanism. Next, the merits and shortcomings of various semiconductors and cocatalysts are summarized, and the strategies for addressing the related issues are also elaborated. Then, various bio‐based feedstocks for solar‐driven H 2 production are reviewed with an emphasis on the effect of photocatalysts and catalytic systems on performance. Of note, the concurrent generation of value‐added chemicals from biomass reforming is emphasized as well. Meanwhile, the emerging photo‐thermal coupling strategy that shows a grand prospect for maximally utilizing the entire solar energy spectrum is also discussed. Further, the direct utilization of hydrogen from biomass as a green reductant for producing value‐added chemicals via organic reactions is also highlighted. Finally, the challenges and perspectives of photoreforming biomass toward hydrogen are envisioned.

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Figure 1 a) Comparison between gray hydrogen from fossil fuels and green hydrogen from sunlight and biomass. b) Schematic illustration of biomass photoreforming to H2 over semiconductor‐based photocatalysts in this review.
Figure 1 a) Comparison between gray hydrogen from fossil fuels and green hydrogen from sunlight and biomass. b) Schematic illustration of biomass photoreforming to H2 over semiconductor‐based photocatalysts in this review.CC BY · PubMed Central
Figure 2 a) Timeline of the mainstream achievements for photocatalytic H2 production from biomass. b) Schematic illustration of photocatalytic reforming of biomass into H2.
Figure 2 a) Timeline of the mainstream achievements for photocatalytic H2 production from biomass. b) Schematic illustration of photocatalytic reforming of biomass into H2.CC BY · PubMed Central
Figure 3 Potential heterogeneous and homogenous photocatalysts for photoreforming of biomass into H2. Reproduced with permission.[ 88 ] Copyright 2022, Cell Press.
Figure 3 Potential heterogeneous and homogenous photocatalysts for photoreforming of biomass into H2. Reproduced with permission.[ 88 ] Copyright 2022, Cell Press.CC BY · PubMed Central
Figure 4 a) Band edge positions and bandgaps with respect to the vacuum level and the normal hydrogen electrode (NHE) for oxides, chalcogenides, nitrides semiconductors and tunable Ga(In, Sb)N band structures in comparison with various semiconductors. Reproduced with permission.[ 112 ] Copyright 2016, Wiley‐VCH. b) Models for single crystal wurtzite GaN nanowires. c) Schematic of the key atomic and electronic structure of the epitaxial GaN. Reproduced with permission.[ 151 ] Copyright 2016, Wiley‐VCH.
Figure 4 a) Band edge positions and bandgaps with respect to the vacuum level and the normal hydrogen electrode (NHE) for oxides, chalcogenides, nitrides semiconductors and tunable Ga(In, Sb)N band structures in comparison with various semiconductors. Reproduced with permission.[ 112 ] Copyright 2016, Wiley‐VCH. b) Models for single crystal wurtzite GaN nanowires. c) Schematic of the key atomic and electronic structure of the epitaxial GaN. Reproduced with permission.[ 151 ] Copyright 2016, Wiley‐VCH.CC BY · PubMed Central
Figure 5 a) Part of the periodic table with highlighted the metals and chalcogenides for constructing of the metal sulfides, b) atomic orbital energies of O, S, Se, and Te, c) illustrative electronic structure of CdS, and d) band positions of some typical oxides and sulfides. Reproduced with permission.[ 125 ] Copyright 2021, Wiley‐VCH. e) Multifunctional characteristics of C3N4 material. Reproduced with permission.[ 136 ] Copyright 2020, the American Chemical Society.
Figure 5 a) Part of the periodic table with highlighted the metals and chalcogenides for constructing of the metal sulfides, b) atomic orbital energies of O, S, Se, and Te, c) illustrative electronic structure of CdS, and d) band positions of some typical oxides and sulfides. Reproduced with permission.[ 125 ] Copyright 2021, Wiley‐VCH. e) Multifunctional characteristics of C3N4 material. Reproduced with permission.[ 136 ] Copyright 2020, the American Chemical Society.CC BY · PubMed Central
Figure 6 a) Schematic illustration of preparing 2D/2D LaVO4/g‐C3N4 photocatalyst for H2 evolution from furfuryl alcohol, and b) photocatalytic mechanism of H2 production over 2D/2D LaVO4/g‐C3N4 heterostructure. Reproduced with permission.[ 143 ] Copyright 2022, Elsevier Inc. c) Structures of COF semiconductors (K denotes knots; L denotes linkers). Reproduced with permission.[ 165 ] Copyright 2020, The Royal Society of Chemistry.
Figure 6 a) Schematic illustration of preparing 2D/2D LaVO4/g‐C3N4 photocatalyst for H2 evolution from furfuryl alcohol, and b) photocatalytic mechanism of H2 production over 2D/2D LaVO4/g‐C3N4 heterostructure. Reproduced with permission.[ 143 ] Copyright 2022, Elsevier Inc. c) Structures of COF semiconductors (K denotes knots; L denotes linkers). Reproduced with permission.[ 165 ] Copyright 2020, The Royal Society of Chemistry.CC BY · PubMed Central
Figure 7 a) Proposed mechanism for photo‐reduction of deposited Pt nanoparticles and photocatalytic H2 evolution over Pt/MIL‐100(Fe). Reproduced with permission.[ 171 ] Copyright 2016, The Royal Society of Chemistry. b) Photogenerated electron transfer and proposed mechanism for photorefining of lignocellulose into H2 over 2% MoS2/TiO2 photocatalyst. Reproduced with permission.[ 205 ] Copyright 2021, Wiley‐VCH.
Figure 7 a) Proposed mechanism for photo‐reduction of deposited Pt nanoparticles and photocatalytic H2 evolution over Pt/MIL‐100(Fe). Reproduced with permission.[ 171 ] Copyright 2016, The Royal Society of Chemistry. b) Photogenerated electron transfer and proposed mechanism for photorefining of lignocellulose into H2 over 2% MoS2/TiO2 photocatalyst. Reproduced with permission.[ 205 ] Copyright 2021, Wiley‐VCH.CC BY · PubMed Central
Figure 8 a) Schematic diagram of the •OH generation on (001) facets of anatase TiO2. b) Comparison of the absorption, activation, and reaction energy for the generation of •OH over (101) and (001) facets of anatase TiO2 and (110) facets of rutile TiO2. c) Reaction path for the generation of •OH over (101) and (001) facets of anatase TiO2 and (110) facets of rutile TiO2. d) Energy diagram of charge transfer and proposed reaction mechanism for photoreforming of lignocelluloses into H2. Reproduced with permission.[ 206 ] Copyright 2022, American Chemical Society.
Figure 8 a) Schematic diagram of the •OH generation on (001) facets of anatase TiO2. b) Comparison of the absorption, activation, and reaction energy for the generation of •OH over (101) and (001) facets of anatase TiO2 and (110) facets of rutile TiO2. c) Reaction path for the generation of •OH over (101) and (001) facets of anatase TiO2 and (110) facets of rutile TiO2. d) Energy diagram of charge transfer and proposed reaction mechanism for photoreforming of lignocelluloses into H2. Reproduced with permission.[ 206 ] Copyright 2022, American Chemical Society.CC BY · PubMed Central
Figure 9 a) Lignocellulose comprised of cellulose, hemicellulose, and lignin, b) Photoreforming of lignocellulose for H2 production over CdS/CdO x , and c) Various raw biomass is photoreformed into H2 production over CdS/CdO x in the alkaline solution. Reproduced with permission.[ 69 ] Copyright 2017, Springer Nature. d) Schematic illustration of photothermal catalytic biomass for hydrogen production. e) Schematic description of a stepwise photoreforming of raw biomass for H2 production. Reproduced with permission.[ 76 ] Copyright 2023, Cell Press.
Figure 9 a) Lignocellulose comprised of cellulose, hemicellulose, and lignin, b) Photoreforming of lignocellulose for H2 production over CdS/CdO x , and c) Various raw biomass is photoreformed into H2 production over CdS/CdO x in the alkaline solution. Reproduced with permission.[ 69 ] Copyright 2017, Springer Nature. d) Schematic illustration of photothermal catalytic biomass for hydrogen production. e) Schematic description of a stepwise photoreforming of raw biomass for H2 production. Reproduced with permission.[ 76 ] Copyright 2023, Cell Press.CC BY · PubMed Central
Figure 10 a) Schematic illustration of lignocellulosic components. Reproduced with permission.[ 218 ] Copyright 2023, American Chemical Society. b) Mechanism of photoreforming of cellulose to H2 in NaOH solution. Reproduced with permission.[ 228 ] Copyright 2021, American Chemical Society.
Figure 10 a) Schematic illustration of lignocellulosic components. Reproduced with permission.[ 218 ] Copyright 2023, American Chemical Society. b) Mechanism of photoreforming of cellulose to H2 in NaOH solution. Reproduced with permission.[ 228 ] Copyright 2021, American Chemical Society.CC BY · PubMed Central
Figure 11 a) Illustration of experimental reactor used for photoreforming cellulose to hydrogen via the combination of photocatalysis and acid hydrolysis, and b) Proposed pathway of cellulose decomposition in combined processes of hydrolysis and photocatalysis. Reproduced with permission.[ 229 ] Copyright 2018, Elsevier Inc. c) Proposed mechanism of cellulose photoreforming toward H2 over P25‐S‐Ni under solar irradiation. Reproduced with permission.[ 231 ] Copyright 2018, Wiley‐VCH.
Figure 11 a) Illustration of experimental reactor used for photoreforming cellulose to hydrogen via the combination of photocatalysis and acid hydrolysis, and b) Proposed pathway of cellulose decomposition in combined processes of hydrolysis and photocatalysis. Reproduced with permission.[ 229 ] Copyright 2018, Elsevier Inc. c) Proposed mechanism of cellulose photoreforming toward H2 over P25‐S‐Ni under solar irradiation. Reproduced with permission.[ 231 ] Copyright 2018, Wiley‐VCH.CC BY · PubMed Central
Figure 12 a) Selective cleavage of β‐aryl ether bond and Cα‐Cβ bond of lignin model compound over SiF/Ni‐NQGDs photocatalysts, b) Products of photoreforming of lignin model compound over SiF/Ni‐NQGDs and SiF, and c) Schematic illustration of lignin photoreforming over SiF/Ni‐NQGDs and SiF. Reproduced with permission.[ 235 ] Copyright 2023, Wiley‐VCH. d) Proposed mechanism of photocatalytic H2 production from biomass over activated NCNCNx with various cocatalysts. Reproduced with permission.[ 70 ] Copyright 2018, American Chemical Society.
Figure 12 a) Selective cleavage of β‐aryl ether bond and Cα‐Cβ bond of lignin model compound over SiF/Ni‐NQGDs photocatalysts, b) Products of photoreforming of lignin model compound over SiF/Ni‐NQGDs and SiF, and c) Schematic illustration of lignin photoreforming over SiF/Ni‐NQGDs and SiF. Reproduced with permission.[ 235 ] Copyright 2023, Wiley‐VCH. d) Proposed mechanism of photocatalytic H2 production from biomass over activated NCNCNx with various cocatalysts. Reproduced with permission.[ 70 ] Copyright 2018, American Chemical Society.CC BY · PubMed Central
Figure 13 High‐resolution C 1s (a) and N 1s (b) XPS spectra of g‐C3N4, PRCN, and Pt NPs/PRCN, c) charge density difference (yellow/green: electron cloud density of N/C), and d) orbital population of g‐C3N4 and PRCN (Blue: N, Gray: C, Purple: K). Reproduced with permission.[ 245 ] Copyright 2022, Elsevier Inc. e) proposed reaction mechanism for photocatalysis of glucose into H2 and lactic acid. Reproduced with permission.[ 247 ] Copyright 2021, Cell Press.
Figure 13 High‐resolution C 1s (a) and N 1s (b) XPS spectra of g‐C3N4, PRCN, and Pt NPs/PRCN, c) charge density difference (yellow/green: electron cloud density of N/C), and d) orbital population of g‐C3N4 and PRCN (Blue: N, Gray: C, Purple: K). Reproduced with permission.[ 245 ] Copyright 2022, Elsevier Inc. e) proposed reaction mechanism for photocatalysis of glucose into H2 and lactic acid. Reproduced with permission.[ 247 ] Copyright 2021, Cell Press.CC BY · PubMed Central
Figure 14 a) The possible reaction route of glucose photoreforming over Zn0.3Cd0.7S. Reproduced with permission.[ 248 ] Copyright 2023, Elsevier Inc. b) Adsorption configurations for various intermediates of methanol photoreforming toward H2 on Ni3Fe/GaN, c) Schematic illustration of methanol photoreforming to generate H2 using NiFe NPs/GaN NWs/Si architecture, and d) Energy profiles for photoreforming of methanol on GaN(101̅0), Ni4/GaN, and Ni3Fe/GaN. Reproduced with permission.[ 160 ] Copyright 2023, the American Chemical Society.
Figure 14 a) The possible reaction route of glucose photoreforming over Zn0.3Cd0.7S. Reproduced with permission.[ 248 ] Copyright 2023, Elsevier Inc. b) Adsorption configurations for various intermediates of methanol photoreforming toward H2 on Ni3Fe/GaN, c) Schematic illustration of methanol photoreforming to generate H2 using NiFe NPs/GaN NWs/Si architecture, and d) Energy profiles for photoreforming of methanol on GaN(101̅0), Ni4/GaN, and Ni3Fe/GaN. Reproduced with permission.[ 160 ] Copyright 2023, the American Chemical Society.CC BY · PubMed Central
Figure 15 a) The possible reaction mechanism of CH3OH photoreforming toward H2 and HCHO over PtCu‐TiO2 photocatalyst. Reproduced with permission.[ 75 ] Copyright 2023, Springer Nature. b) Schematic illustration of solar‐driven methanol reforming into hydrogen via synergetic photo‐ and thermocatalysis. Reproduced with permission.[ 272 ] Copyright 2021, Elsevier Inc. c) Triggering water and methanol activation for solar‐driven H2 production over plasmonic ZnCu alloy via photo‐thermal‐catalysis. Reproduced with permission.[ 73 ] Copyright 2021, the American Chemical Society. d) Schematics of the outdoor flow solar‐heating thermocatalysis of methanol reforming into H2. Reproduced with permission.[ 275 ] Copyright 2023, Elsevier Inc.
Figure 15 a) The possible reaction mechanism of CH3OH photoreforming toward H2 and HCHO over PtCu‐TiO2 photocatalyst. Reproduced with permission.[ 75 ] Copyright 2023, Springer Nature. b) Schematic illustration of solar‐driven methanol reforming into hydrogen via synergetic photo‐ and thermocatalysis. Reproduced with permission.[ 272 ] Copyright 2021, Elsevier Inc. c) Triggering water and methanol activation for solar‐driven H2 production over plasmonic ZnCu alloy via photo‐thermal‐catalysis. Reproduced with permission.[ 73 ] Copyright 2021, the American Chemical Society. d) Schematics of the outdoor flow solar‐heating thermocatalysis of methanol reforming into H2. Reproduced with permission.[ 275 ] Copyright 2023, Elsevier Inc.CC BY · PubMed Central
Figure 16 a) Schematic demonstration of the relative energy levels of TiO2 and CoTiO3 and a charge migration mechanism between TiO2 and CoTiO3 in a type II heterostructure and a direct Z‐scheme. Reproduced with permission.[ 282 ] Copyright 2021, the American Chemical Society. b) Schematic illustration of solar hydrogen production from ethanol‐water over metal/TiO2 photocatalysts supported on β‐SiC alveolar foams. Reproduced with permission.[ 284 ] Copyright 2023, Elsevier Inc. c) Schematic illustration of photoreforming of ethanol into DEE and H2 over PdPSA‐CdS. Reproduced with permission.[ 295 ] Copyright 2021, Cell Press. d) Schematic demonstration of the photothermal device of Ni SA/CeO2‐Ti2O3/Cu for solar‐driven H2 evolution from ethanol, e) TEM cross‐section of a Ti2O3/Cu film, and f) Schematic of the synthesis process for the Ni SA/CeO2 nanosheets. Reproduced with permission.[ 292 ] Copyright 2022, The Royal Society of Chemistry.
Figure 16 a) Schematic demonstration of the relative energy levels of TiO2 and CoTiO3 and a charge migration mechanism between TiO2 and CoTiO3 in a type II heterostructure and a direct Z‐scheme. Reproduced with permission.[ 282 ] Copyright 2021, the American Chemical Society. b) Schematic illustration of solar hydrogen production from ethanol‐water over metal/TiO2 photocatalysts supported on β‐SiC alveolar foams. Reproduced with permission.[ 284 ] Copyright 2023, Elsevier Inc. c) Schematic illustration of photoreforming of ethanol into DEE and H2 over PdPSA‐CdS. Reproduced with permission.[ 295 ] Copyright 2021, Cell Press. d) Schematic demonstration of the photothermal device of Ni SA/CeO2‐Ti2O3/Cu for solar‐driven H2 evolution from ethanol, e) TEM cross‐section of a Ti2O3/Cu film, and f) Schematic of the synthesis process for the Ni SA/CeO2 nanosheets. Reproduced with permission.[ 292 ] Copyright 2022, The Royal Society of Chemistry.CC BY · PubMed Central
Figure 17 a) Synthesis routes of Au/TiO2, mono‐Au@SiO2/TiO2, and multi‐Au@SiO2/TiO2, and b) Mechanism of photoreforming ethanol into DEE and H2 over Multi‐Au@SiO2/TiO2. Reproduced with permission.[ 296 ] Copyright 2020, American Chemical Society. c) Mechanistic illustration of photocatalytic co‐production of DEE and H2 over the Pt/UCN/Nb2O5‐(2) photocatalyst. Reproduced with permission.[ 299 ] Copyright 2022, The Royal Society of Chemistry.
Figure 17 a) Synthesis routes of Au/TiO2, mono‐Au@SiO2/TiO2, and multi‐Au@SiO2/TiO2, and b) Mechanism of photoreforming ethanol into DEE and H2 over Multi‐Au@SiO2/TiO2. Reproduced with permission.[ 296 ] Copyright 2020, American Chemical Society. c) Mechanistic illustration of photocatalytic co‐production of DEE and H2 over the Pt/UCN/Nb2O5‐(2) photocatalyst. Reproduced with permission.[ 299 ] Copyright 2022, The Royal Society of Chemistry.CC BY · PubMed Central
Figure 18 a) The overall mechanism of PHE over BiOCl@ZIS/Pt composite under visible light irradiation. Reproduced with permission.[ 301 ] Copyright 2023, Elsevier Inc. b) Catalyst screening for photocatalytic glycerol reforming, and c) Comparison of catalytic activity between CdS and CdO‐QDs/CdS catalysts. Reproduced with permission.[ 307 ] Copyright 2022, Cell Press. d) Mechanism of the photocatalytic reforming of glycerol on CdS‐Cl. Reproduced with permission.[ 309 ] Copyright 2023, Wiley‐VCH.
Figure 18 a) The overall mechanism of PHE over BiOCl@ZIS/Pt composite under visible light irradiation. Reproduced with permission.[ 301 ] Copyright 2023, Elsevier Inc. b) Catalyst screening for photocatalytic glycerol reforming, and c) Comparison of catalytic activity between CdS and CdO‐QDs/CdS catalysts. Reproduced with permission.[ 307 ] Copyright 2022, Cell Press. d) Mechanism of the photocatalytic reforming of glycerol on CdS‐Cl. Reproduced with permission.[ 309 ] Copyright 2023, Wiley‐VCH.CC BY · PubMed Central
Figure 19 Proposed reaction mechanism for a) photocatalytic H2 generation from glycerol aqueous solution and b) H2 evolution from H2S over the ZCNS core‐shell nanocomposite. Reproduced with permission.[ 310 ] Copyright 2021, Elsevier Inc.
Figure 19 Proposed reaction mechanism for a) photocatalytic H2 generation from glycerol aqueous solution and b) H2 evolution from H2S over the ZCNS core‐shell nanocomposite. Reproduced with permission.[ 310 ] Copyright 2021, Elsevier Inc.CC BY · PubMed Central
Figure 20 Green syngas production from glycerol, water, and sunlight over AuIn NPs/GaN NWs/Si. a) The syngas activities of several possible C2 and C3 intermediates. b) Calculated free‐energy diagram for glycerol reforming. c) Photocatalytic glycerol reforming. d) Schematic illustration of syngas production from glycerol and water. Reproduced with permission.[ 314 ] Copyright 2023, The Royal Society of Chemistry.
Figure 20 Green syngas production from glycerol, water, and sunlight over AuIn NPs/GaN NWs/Si. a) The syngas activities of several possible C2 and C3 intermediates. b) Calculated free‐energy diagram for glycerol reforming. c) Photocatalytic glycerol reforming. d) Schematic illustration of syngas production from glycerol and water. Reproduced with permission.[ 314 ] Copyright 2023, The Royal Society of Chemistry.CC BY · PubMed Central
Figure 21 a) Proposed mechanism of photothermal reforming of glycerol over 2D Au/TiO2. Reproduced with permission.[ 315 ] Copyright 2021, Elsevier Inc. b) Carbon cycle for utilization of formic acid as a LOHC. Reproduced with permission.[ 319 ] Copyright 2023, Cell Press. c) Proposed mechanism for hydrogen production from formic acid photoreforming over Ni/CdS QDs. Reproduced with permission.[ 333 ] Copyright 2023, Wiley‐VCH. d) Proposed mechanism for photocatalytic H2 production from formic acid over 0.5% MoS2/Zn3In2S6. Reproduced with permission.[ 335 ] Copyright 2021, Elsevier Inc.
Figure 21 a) Proposed mechanism of photothermal reforming of glycerol over 2D Au/TiO2. Reproduced with permission.[ 315 ] Copyright 2021, Elsevier Inc. b) Carbon cycle for utilization of formic acid as a LOHC. Reproduced with permission.[ 319 ] Copyright 2023, Cell Press. c) Proposed mechanism for hydrogen production from formic acid photoreforming over Ni/CdS QDs. Reproduced with permission.[ 333 ] Copyright 2023, Wiley‐VCH. d) Proposed mechanism for photocatalytic H2 production from formic acid over 0.5% MoS2/Zn3In2S6. Reproduced with permission.[ 335 ] Copyright 2021, Elsevier Inc.CC BY · PubMed Central
Figure 22 a) Schematic illustration of the CdS/CoP@RGO. b) Proposed mechanism for photocatalytic H2 production from formic acid over CdS/CoP@RGO. Reproduced with permission.[ 340 ] Copyright 2018, Cell Press.
Figure 22 a) Schematic illustration of the CdS/CoP@RGO. b) Proposed mechanism for photocatalytic H2 production from formic acid over CdS/CoP@RGO. Reproduced with permission.[ 340 ] Copyright 2018, Cell Press.CC BY · PubMed Central
Figure 23 a) Schematic illustration of photocatalytic reduction of nitrobenzene to aniline coupled with oxidation of glycerol to fine chemicals over Pd/TiO2. Reproduced with permission. Reproduced with permission.[ 349 ] Copyright 2015, The Royal Society of Chemistry. b) Schematic diagram of visible‐light‐driven simultaneous conversion of glucose to arabinose and nitrosobenzene to azoxybenzene over Pd/Meso CdS. Reproduced with permission.[ 350 ] Copyright 2016, The Royal Society of Chemistry. c) Proposed mechanism for photoconversion of the lignin model via self‐hydrogen transfer hydrogenolysis. Reproduced with permission.[ 352 ] Copyright 2017, American Chemical Society. d) Proposed mechanism for photocatalytic deoxygenation of aromatic ketones using ethanol as a hydrogen donor over Pd/TiO2 photocatalyst. Reproduced with permission. Reproduced with permission.[ 353 ] Copyright 2020, The Royal Society of Chemistry.
Figure 23 a) Schematic illustration of photocatalytic reduction of nitrobenzene to aniline coupled with oxidation of glycerol to fine chemicals over Pd/TiO2. Reproduced with permission. Reproduced with permission.[ 349 ] Copyright 2015, The Royal Society of Chemistry. b) Schematic diagram of visible‐light‐driven simultaneous conversion of glucose to arabinose and nitrosobenzene to azoxybenzene over Pd/Meso CdS. Reproduced with permission.[ 350 ] Copyright 2016, The Royal Society of Chemistry. c) Proposed mechanism for photoconversion of the lignin model via self‐hydrogen transfer hydrogenolysis. Reproduced with permission.[ 352 ] Copyright 2017, American Chemical Society. d) Proposed mechanism for photocatalytic deoxygenation of aromatic ketones using ethanol as a hydrogen donor over Pd/TiO2 photocatalyst. Reproduced with permission. Reproduced with permission.[ 353 ] Copyright 2020, The Royal Society of Chemistry.CC BY · PubMed Central

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Items 201–349 of 349

Research works printed but not linked: 10

  1. Melo M. D. O., 2011, J. Brazil. Chem. Soc., 22, 1399
  2. Zhang Y., 2019, Chem, 1
  3. Kreft S., 2020, Chem, 2
  4. Reddy N. S., 2023, Nano Energy, 11
  5. Zhou B., 2023, Sci. China Chem., 66, 739
  6. Li X., 2023, J Mater Chem, 11, 3235
  7. Rodríguez‐Lugo R. E., 2013, Chem, 5, 342
  8. Jawhari A. H., 2023, Fuel Process. Technol., 344
  9. Wang Z., 2024, Angew. Chem., Int. Ed.
  10. Kondarides D., 2010, J. Adv. Oxid. Technol., 13, 116

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Metadata

Authors
Pan, H., Li, J., Wang, Y., Xia, Q., Qiu, L., & Zhou, B.
Affiliations
  • College of Biological Chemical Science and Engineering Jiaxing University 899 Guangqiong Road Jiaxing Zhejiang 314001 China
  • Shanghai Jiao Tong University (CN)
  • Jiaxing University (CN)
Corresponding author
  • Wang, Yangang
  • Zhou, Baowen
ORCID
Venue
Advanced Science
Publisher
Wiley
Published
2024-05-30
Volume
11
Issue
29
Pages
e2402651-e2402651
ISSN
2198-3844 (ISSN-L)
DOI
10.1002/advs.202402651
PMC
PMC11304308
OpenAlex
W4399246574
Cited by
67
References
350
Citations by year
2026: 26 · 2025: 32 · 2024: 9
FWCI
1.40
Type
journal article
Language
en
Open access
Licence
Locations
  • Advanced Science (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Funders
  • Natural Science Foundation of Zhejiang Province (LQ22B060008)
  • National Natural Science Foundation of China (22109095, 22278176)
  • National Key Research and Development Program of China (2023YFB4004900)
Topics
  • Physical Sciences › Energy › Renewable Energy, Sustainability and the Environment › Advanced Photocatalysis Techniques
  • Physical Sciences › Chemical Engineering › Catalysis › Catalysis for Biomass Conversion
  • Physical Sciences › Energy › Fuel Technology › Thermochemical Biomass Conversion Processes
Keywords
solar hydrogen production, photocatalytic hydrogen evolution, semiconductors, cocatalyst, bio-based feedstocks, value-added chemicals, organic reactions, carbon neutrality, organic solid waste

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