Frustrated Lewis Pairs and Metallic Ni Synergistically Enabled Low‐Temperature Hydrogenolysis of Lignin Models
Source abstract
Abstract
ABSTRACT Low‐temperature hydrogenolysis of aromatic ether bonds is a highly promising strategy to convert lignin. However, it remains highly challenging to enable this strategy over non‐noble metal‐based catalysts. Herein, Ni and Al mixed oxide catalysts (denoted as NiAlO x ‐T, where T represented the reduction temperature) were constructed by the reduction of layered Ni‐Al hydroxides. Interestingly, the NiAlO x ‐300 could efficiently promote the hydrogenolysis of various lignin models (i.e., α‐O‐4 referring to benzyl phenyl ether linkage (C α ‐O‐Ar), β‐O‐4 referring to 2‐phenoxy‐1‐phenylethanol linkage (C β ‐O‐Ar), and 4‐O‐5 referring to diphenyl ether linkage (Ar‐O‐Ar)) at a temperature of ≤ 100°C. Notably, benzyl phenyl ether (a typical α‐O‐4 model) could be converted into toluene and phenol at 20°C. Systematic analysis revealed that abundant solid surface frustrated Lewis pairs (ssFLPs) composed by unsaturated Al sites (Al 3+ unsatur. ) proximal to a surface oxygen vacancy and surface Lewis basic OH were generated in NiAlO x ‐300. The excellent performance of the NiAlO x ‐300 catalyst originated from the synergistic effect of ssFLPs sites and metallic Ni 0 sites, which was beneficial to efficient hydrogen activation for hydrogenolysis of lignin models at mild conditions. This work provided a new kind of non‐noble metal‐based catalyst for lignin valorization by creating solid surface frustrated Lewis pairs cooperated with non‐noble metals.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Lignin and Wood Chemistry · Catalysis for Biomass Conversion · Plant-derived Lignans Synthesis and Bioactivity
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Chemical Engineering and Light Industry Guangdong University of Technology Guangzhou China
State Key Laboratory of Efficient Production of Forest Resources College of Materials Science and Technology Beijing Forestry University Beijing China
National & Local Joint Engineering Research Center on Biomass Resource Utilization College of Environmental Science and Engineering Nankai University Tianjin China
Funding
National Natural Science Foundation of China · National Key Research and Development Program of China
References (75)
Show source-provided references
1. 10.1021/acs.chemrev.5b0015510.1021/acs.chemrev.5b00155 ↗
2. 10.1039/D1CS00908G10.1039/D1CS00908G ↗
3. 10.1021/cr900354u10.1021/cr900354u ↗
4. 10.1039/C1CS15147A10.1039/C1CS15147A ↗
5. 10.1039/D0CS00134A10.1039/D0CS00134A ↗
6. 10.1021/acs.chemrev.7b0058810.1021/acs.chemrev.7b00588 ↗
7. 10.1002/anie.20151035110.1002/anie.201510351 ↗
8. 10.1039/C4CS00235K10.1039/C4CS00235K ↗
9. 10.1039/D0CS00078G10.1039/D0CS00078G ↗
10. 10.1016/j.rser.2017.01.16610.1016/j.rser.2017.01.166 ↗
11. 10.1021/acscatal.6b0050210.1021/acscatal.6b00502 ↗
12. 10.1021/acssuschemeng.8b0159310.1021/acssuschemeng.8b01593 ↗
13. 10.1038/ncomms1419010.1038/ncomms14190 ↗
14. 10.1002/anie.20161107610.1002/anie.201611076 ↗
15. 10.1002/anie.20171221110.1002/anie.201712211 ↗
16. 10.1016/j.jechem.2023.01.01410.1016/j.jechem.2023.01.014 ↗
17. 10.1002/anie.20210132510.1002/anie.202101325 ↗
18. 10.1021/acscatal.2c0218810.1021/acscatal.2c02188 ↗
19. 10.1021/acssuschemeng.7b0299310.1021/acssuschemeng.7b02993 ↗
20. 10.1002/cctc.20240182810.1002/cctc.202401828 ↗
21. 10.1016/j.jcat.2025.11613710.1016/j.jcat.2025.116137 ↗
22. 10.1002/cssc.20200097810.1002/cssc.202000978 ↗
23. 10.1021/acscatal.1c0399910.1021/acscatal.1c03999 ↗
24. K.Oshida K.Yuan Y.Yamazaki et al. “Hydrogen‐Induced Formation of Surface Acid Sites on Pt/Al(PO3)3Enables Remarkably Efficient Hydrogenolysis of C‐O Bonds in Alcohols and Ethers ”63(2024):202403092.10.1002/anie.202403092 ↗
25. 10.1021/acssuschemeng.2c0203810.1021/acssuschemeng.2c02038 ↗
26. 10.1016/j.fuproc.2020.10639210.1016/j.fuproc.2020.106392 ↗
27. 10.1021/cs401199f10.1021/cs401199f ↗
28. 10.1016/j.renene.2019.10.16010.1016/j.renene.2019.10.160 ↗
29. 10.1016/j.cej.2023.14518210.1016/j.cej.2023.145182 ↗
30. 10.1021/ja309915e10.1021/ja309915e ↗
31. 10.1002/anie.20150913310.1002/anie.201509133 ↗
32. Catalytic Hydroconversion of Two Lignin‐Related Model Compounds Over Ni/CeO210.1016/j.fuel.2022.125808 ↗
33. 10.1021/acscatal.2c0152310.1021/acscatal.2c01523 ↗
34. 10.1021/acscatal.4c0453710.1021/acscatal.4c04537 ↗
35. 10.1039/D1TA08916A10.1039/D1TA08916A ↗
36. 10.1021/jacs.4c1710310.1021/jacs.4c17103 ↗
37. 10.1021/jacs.2c1348710.1021/jacs.2c13487 ↗
38. 10.1021/acscatal.4c0237810.1021/acscatal.4c02378 ↗
39. 10.1038/s41467‐025‐61851‐610.1038/s41467‐025‐61851‐6 ↗
40. 10.1038/s41467‐022‐29970‐610.1038/s41467‐022‐29970‐6 ↗
41. 10.1021/acs.energyfuels.5c0364310.1021/acs.energyfuels.5c03643 ↗
42. 10.1039/C4CS00160E10.1039/C4CS00160E ↗
43. 10.1039/C7CS00318H10.1039/C7CS00318H ↗
44. 10.1002/adfm.20170386810.1002/adfm.201703868 ↗
45. 10.1021/acscatal.0c0416210.1021/acscatal.0c04162 ↗
46. 10.1038/s41467‐023‐37631‐510.1038/s41467‐023‐37631‐5 ↗
47. 10.1002/adma.20170001710.1002/adma.201700017 ↗
48. 10.1021/acscatal.4c0249310.1021/acscatal.4c02493 ↗
49. 10.1021/jacs.4c0032710.1021/jacs.4c00327 ↗
50. 10.1039/C5GC00062A10.1039/C5GC00062A ↗
51. 10.1039/D3GC04217K10.1039/D3GC04217K ↗
52. 10.1039/C9SC00691E10.1039/C9SC00691E ↗
53. Highly Efficient Catalytic Hydrogenolysis of Lignin Model Compounds Over Hydrotalcite‐Derived Ni/Al2O3 Catalysts10.1016/j.fuel.2022.127196 ↗
54. 10.1021/acscatal.6b0349410.1021/acscatal.6b03494 ↗
55. 10.1002/anie.20210549210.1002/anie.202105492 ↗
56. 10.1021/acscatal.4c0667510.1021/acscatal.4c06675 ↗
57. 10.1021/acscatal.9b0159710.1021/acscatal.9b01597 ↗
58. 10.1016/j.apcatb.2014.08.01710.1016/j.apcatb.2014.08.017 ↗
59. 10.1039/C9TA12768B10.1039/C9TA12768B ↗
60. 10.1016/j.jcis.2020.05.03210.1016/j.jcis.2020.05.032 ↗
61. 10.1016/j.jcis.2023.10.05910.1016/j.jcis.2023.10.059 ↗
62. 10.1016/j.jcat.2012.10.01210.1016/j.jcat.2012.10.012 ↗
63. 10.1016/j.apcatb.2021.12019110.1016/j.apcatb.2021.120191 ↗
64. 10.1021/acs.jpclett.0c0376010.1021/acs.jpclett.0c03760 ↗
65. 10.1021/jacs.5b1017910.1021/jacs.5b10179 ↗
66. 10.1016/j.apcatb.2020.11933610.1016/j.apcatb.2020.119336 ↗
67. 10.1016/j.apcatb.2016.10.00910.1016/j.apcatb.2016.10.009 ↗
68. Propane Dehydrogenation over Pt/TiO2–Al2O3 Catalysts10.1021/cs501279v ↗
69. 10.1016/j.apcata.2022.11848110.1016/j.apcata.2022.118481 ↗
70. 10.1021/cr300418s10.1021/cr300418s ↗
71. 10.1021/acscatal.4c0531410.1021/acscatal.4c05314 ↗
72. 10.1002/anie.20230268410.1002/anie.202302684 ↗
73. 10.1021/acscatal.6b0101510.1021/acscatal.6b01015 ↗
74. 10.1021/acscatal.3c0230310.1021/acscatal.3c02303 ↗
75. 10.1021/acssuschemeng.3c0471310.1021/acssuschemeng.3c04713 ↗