journal article·2024-06Open access

Reduction of 5‐Hydroxymethylfurfural to 2,5‐Bis(hydroxymethyl)Furan at High Current Density using a Ga‐Doped AgCu:Cationomer Hybrid Electrocatalyst

Cong Tian, Jiaqi Yu, Daojin Zhou, Huajie Ze, Hengzhou Liu, Yuanjun Chen, Rong Xia, Pengfei Ou, Weiyan Ni, Ke Xie, Edward H. Sargent

Advanced Materials· Volume 36· Issue 24

Abstract

Abstract Hydrogenation of biomass‐derived chemicals is of interest for the production of biofuels and valorized chemicals. Thermochemical processes for biomass reduction typically employ hydrogen as the reductant at elevated temperatures and pressures. Here, the authors investigate the direct electrified reduction of 5‐hydroxymethylfurfural (HMF) to a precursor to bio‐polymers, 2,5‐bis(hydroxymethyl)furan (BHMF). Noting a limited current density in prior reports of this transformation, a hybrid catalyst consisting of ternary metal nanodendrites mixed with a cationic ionomer, the latter purposed to increase local pH and facilitate surface proton diffusion, is investigated. This approach, when implemented using Ga‐doped Ag‐Cu electrocatalysts designed for p–d orbital hybridization, steered selectivity to BHMF, achieving a faradaic efficiency (FE) of 58% at 100 mA cm−2 and a production rate of 1 mmol cm−2 h−1, the latter a doubling in rate compared to the best prior reports.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Catalysis for Biomass Conversion · Electrocatalysts for Energy Conversion · Advanced battery technologies research

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Chemistry Northwestern University 2145 Sheridan Rd Evanston IL 60208 USA

Department of Electrical and Computer Engineering Northwestern University 2145 Sheridan Rd Evanston IL 60208 USA

Funding

National Science Foundation

References (30)

Show source-provided references
1. 10.1021/acs.chemrev.0c0015810.1021/acs.chemrev.0c00158 ↗
2. 10.1126/science.abg237110.1126/science.abg2371 ↗
3. 10.1021/acs.chemrev.2c0067310.1021/acs.chemrev.2c00673 ↗
4. 10.1039/b922014c10.1039/b922014c ↗
5. 10.1021/acscatal.2c0360610.1021/acscatal.2c03606 ↗
6. 10.1021/acscatal.3c0227210.1021/acscatal.3c02272 ↗
7. 10.1002/cssc.20210250410.1002/cssc.202102504 ↗
8. 10.1021/acsami.1c0289610.1021/acsami.1c02896 ↗
9. 10.1002/celc.20190216110.1002/celc.201902161 ↗
10. 10.1021/acscatal.5b0258610.1021/acscatal.5b02586 ↗
11. 10.1002/cssc.20130044310.1002/cssc.201300443 ↗
12. 10.1038/s41467-023-41497-y10.1038/s41467-023-41497-y ↗
13. 10.1002/celc.20210066210.1002/celc.202100662 ↗
14. 10.1039/D1GC00988E10.1039/D1GC00988E ↗
15. 10.1002/anie.20210739010.1002/anie.202107390 ↗
16. 10.1002/adma.20200705610.1002/adma.202007056 ↗
17. 10.1126/science.aav350610.1126/science.aav3506 ↗
18. 10.1021/jacs.2c1274310.1021/jacs.2c12743 ↗
19. 10.1002/anie.20211573510.1002/anie.202115735 ↗
20. 10.1038/s41929-023-01003-510.1038/s41929-023-01003-5 ↗
21. 10.1038/s41560-021-00920-810.1038/s41560-021-00920-8 ↗
22. 10.1126/science.aay421710.1126/science.aay4217 ↗
23. 10.1016/j.mcat.2022.11248710.1016/j.mcat.2022.112487 ↗
24. 10.1002/cssc.20210157510.1002/cssc.202101575 ↗
25. 10.1038/s44160-023-00259-w10.1038/s44160-023-00259-w ↗
26. 10.1002/cssc.20220095210.1002/cssc.202200952 ↗
27. 10.1039/C9CC06646B10.1039/C9CC06646B ↗
28. 10.1039/D0SC00136H10.1039/D0SC00136H ↗
29. 10.1002/anie.20220984910.1002/anie.202209849 ↗
30. 10.1038/nmat175210.1038/nmat1752 ↗