TY - JOUR
T1 - On-Demand, Highly Tunable, and Selective 5-Hydroxymethylfurfural Hydrogenation to Furan Diols Enabled by Ni and Ni3Ga Alloy Catalysts
AU - Zhang, Yongsheng
AU - Rezayan, Armin
AU - Wang, Ke
AU - Wang, Jianshe
AU - Xu, Chunbao Charles
AU - Nie, Renfeng
PY - 2023/1/6
Y1 - 2023/1/6
N2 - Catalytic conversion of the biobased platform chemical 5-hydroxymethylfurfural (HMF) into high-value-added products (e.g., diols) has attracted considerable attention, where controlling the products’ selectivity is a crucial and challenging issue. Herein, a series of hydrotalcite-based Ni and Ni3Ga alloy catalysts were prepared for HMF hydrogenation into furan diols. By optimizing the loaded metal and reduction temperature, >99% BHMTHF and 95.6% BHMF yields were gained over Ni1.5Al-LDO-700 and Ni1.5GaAl-LDO-700, respectively, under mild conditions. Characterizations and DFT calculations showed that the doped Ga resulted in charge transfer from Ga to Ni and disrupted the Ni arrangement, which weakened the furan ring adsorption and favored its tilted adsorption on the Ni3Ga alloy, consequently inhibited deep hydrogenation, and selectively produced BHMF. These catalysts were also versatile for hydrogenation of other furan aldehydes, achieving high selectivity toward un-/saturated alcohols on demand. This study provides an advanced strategy for the rational design of superior catalysts for tuning product selectivity on demand, with practical potential for upgrading biomass-derived platform molecules. © 2022 American Chemical Society.
AB - Catalytic conversion of the biobased platform chemical 5-hydroxymethylfurfural (HMF) into high-value-added products (e.g., diols) has attracted considerable attention, where controlling the products’ selectivity is a crucial and challenging issue. Herein, a series of hydrotalcite-based Ni and Ni3Ga alloy catalysts were prepared for HMF hydrogenation into furan diols. By optimizing the loaded metal and reduction temperature, >99% BHMTHF and 95.6% BHMF yields were gained over Ni1.5Al-LDO-700 and Ni1.5GaAl-LDO-700, respectively, under mild conditions. Characterizations and DFT calculations showed that the doped Ga resulted in charge transfer from Ga to Ni and disrupted the Ni arrangement, which weakened the furan ring adsorption and favored its tilted adsorption on the Ni3Ga alloy, consequently inhibited deep hydrogenation, and selectively produced BHMF. These catalysts were also versatile for hydrogenation of other furan aldehydes, achieving high selectivity toward un-/saturated alcohols on demand. This study provides an advanced strategy for the rational design of superior catalysts for tuning product selectivity on demand, with practical potential for upgrading biomass-derived platform molecules. © 2022 American Chemical Society.
KW - 5-hydroxymethylfurfural
KW - furan diol
KW - Ni3Ga alloy
KW - on-demand hydrogenation
KW - structure−selectivity correlation
UR - http://www.scopus.com/inward/record.url?scp=85145592309&partnerID=8YFLogxK
UR - https://www.scopus.com/record/pubmetrics.uri?eid=2-s2.0-85145592309&origin=recordpage
U2 - 10.1021/acscatal.2c05451
DO - 10.1021/acscatal.2c05451
M3 - RGC 21 - Publication in refereed journal
SN - 2155-5435
VL - 13
SP - 803
EP - 814
JO - ACS Catalysis
JF - ACS Catalysis
IS - 1
ER -