TY - JOUR
T1 - Engineered N/O-doped hierarchical porous carbons from coffee grounds for high-performance supercapacitors
AU - Du, Yuhan
AU - Cao, Changqing
AU - Chen, Lei
AU - Jiang, Zhao
AU - Duan, Peigao
N1 - Publisher Copyright:
© 2025 Elsevier B.V.
PY - 2025/12/15
Y1 - 2025/12/15
N2 - This study presents a hydrothermal-activation strategy to convert coffee grounds into N/O co-doped hierarchical porous carbons (ACG-X) for high-performance supercapacitors. Hydrothermal carbonization transforms biomass into aromatic-rich carbon skeletons while converting inherent N/O heteroatoms into electrochemically active groups (CdbndO and N-5), and subsequent KOH activation constructs a 3D hierarchical porous network (2473.15 m2·g−1 surface area). The optimized material achieves exceptional electrochemical performance: a specific capacitance of 546.08 F·g−1 at 0.5 A·g−1 (74.6 % retention at 10 A·g−1) and symmetric supercapacitors delivering 16.48 Wh·kg−1 energy density at 125.03 W·kg−1 in 6 M KOH electrolyte, surpassing most reported biomass-derived carbons. Key innovations include (1) synergistic pore-heteroatom engineering via hydrothermal pretreatment and activation, (2) dual charge storage from electric double-layer capacitance (hierarchical pores) and pseudocapacitance (N/O functionalities), and (3) scalable waste-to-energy conversion with 81.19 % capacitance retention after 15,000 cycles. The work provides mechanistic insights into heteroatom-pore structure synergy during biomass conversion, establishing a paradigm for controllable synthesis of high-performance energy storage materials.
AB - This study presents a hydrothermal-activation strategy to convert coffee grounds into N/O co-doped hierarchical porous carbons (ACG-X) for high-performance supercapacitors. Hydrothermal carbonization transforms biomass into aromatic-rich carbon skeletons while converting inherent N/O heteroatoms into electrochemically active groups (CdbndO and N-5), and subsequent KOH activation constructs a 3D hierarchical porous network (2473.15 m2·g−1 surface area). The optimized material achieves exceptional electrochemical performance: a specific capacitance of 546.08 F·g−1 at 0.5 A·g−1 (74.6 % retention at 10 A·g−1) and symmetric supercapacitors delivering 16.48 Wh·kg−1 energy density at 125.03 W·kg−1 in 6 M KOH electrolyte, surpassing most reported biomass-derived carbons. Key innovations include (1) synergistic pore-heteroatom engineering via hydrothermal pretreatment and activation, (2) dual charge storage from electric double-layer capacitance (hierarchical pores) and pseudocapacitance (N/O functionalities), and (3) scalable waste-to-energy conversion with 81.19 % capacitance retention after 15,000 cycles. The work provides mechanistic insights into heteroatom-pore structure synergy during biomass conversion, establishing a paradigm for controllable synthesis of high-performance energy storage materials.
KW - Biomass-derived supercapacitor
KW - Heteroatom-pore synergy
KW - High specific capacitance
KW - Hydrothermal-activation synergy
KW - N/O co-doped porous carbon
UR - https://www.scopus.com/pages/publications/105022206802
U2 - 10.1016/j.cej.2025.170934
DO - 10.1016/j.cej.2025.170934
M3 - 文章
AN - SCOPUS:105022206802
SN - 1385-8947
VL - 526
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
M1 - 170934
ER -