Keyword search (4,163 papers available)

"Hao Y" Authored Publications:

Title Authors PubMed ID
1 An active bifunctional natural dye for stable all-solid-state organic batteries Yu Q; Hu Y; Deng S; Shakouri M; Chen J; Martins V; Nie HY; Huang Y; Zhao Y; Zaghib K; Sham TK; Li X; 40993135
PHYSICS
2 Solid solvation structure design improves all-solid-state organic batteries Hu Y; Su H; Fu J; Luo J; Yu Q; Zhao F; Li W; Deng S; Liu Y; Yuan Y; Gan Y; Wang Y; Kim JT; Chen N; Shakouri M; Hao X; Gao Y; Pang T; Zhang N; Jiang M; Li X; Zhao Y; Tu J; Wang C; Sun X; 40759737
ENCS
3 Study on the mechanism of regulating micromolar Fe utilization and promoting denitrification by guanosine monophosphate (GMP) based multi-signal functional material Hematin@Fe/GMP Hao Y; Guo T; Li H; Liu W; Chen Z; Wang X; Guo J; 39657473
ENCS
4 Fe/GMP functional nanomaterial enhancing the denitrification efficiency by bi-signal regulation: Electron transfer and microbial community Hao Y; Guo T; Li H; Liu W; Chen Z; Zhang W; Wang X; Guo J; 39326537
ENCS
5 Exploring the use of ceramic disk filter coated with Ag/ZnO nanocomposites as an innovative approach for removing Escherichia coli from household drinking water. Huang J, Huang G, An C, Xin X, Chen X, Zhao Y, Feng R, Xiong W 31864067
ENCS
6 Enhanced nitrogen removal in the treatment of rural domestic sewage using vertical-flow multi-soil-layering systems: Experimental and modeling insights. Hong Y, Huang G, An C, Song P, Xin X, Chen X, Zhang P, Zhao Y, Zheng R 30952048
ENCS

 

Title:An active bifunctional natural dye for stable all-solid-state organic batteries
Authors:Yu QHu YDeng SShakouri MChen JMartins VNie HYHuang YZhao YZaghib KSham TKLi X
Link:https://pubmed.ncbi.nlm.nih.gov/40993135/
DOI:10.1038/s41467-025-62301-z
Publication:Nature communications
Keywords:
PMID:40993135 Category: Date Added:2025-09-25
Dept Affiliation: PHYSICS
1 Department of Chemical and Materials Engineering, Concordia University, Montreal, Quebec, Canada.
2 Department of Mechanical, Industrial & Aerospace Engineering, Concordia University, Montreal, Quebec, Canada.
3 Department of Mechanical and Materials Engineering, University of Western Ontario, London, Ontario, Canada.
4 Canadian Light Source Inc., University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
5 Department of Chemistry, University of Western Ontario, London, Ontario, Canada.
6 Surface Science Western, University of Western Ontario, 999 Collip Circle, London, Ontario, Canada.
7 Department of Physics and Astronomy, University of Western Ontario, 1151 Richmond St, London, Ontario, Canada.
8 Department of Chemical and Materials Engineering, Concordia University, Montreal, Quebec, Canada. xia.li@concordia.ca.

Description:

Sustainable and cost-effective organic electrode materials are promising for next-generation lithium-ion batteries but are hindered by severe shuttle effects. While all-solid-state batteries offer a potential solution, chemical and mechanical incompatibility between organic electrode materials and inorganic solid electrolytes limit areal capacity and cycling stability, falling short of practical requirements. Here, we report a bifunctional indigo natural dye that serves as both an active material and a solid molecular catalyst in sulfide-based all-solid-state batteries, addressing these compatibility challenges. Contrary to the prevailing view that chemical reactions between organic electrode materials and sulfide solid electrolytes are detrimental, our study reveals that controlled reactions between indigo and Li6PS5Cl solid electrolyte catalyze their synergistic redox process after optimizing electrode microstructures. This strategy enables a high reversible capacity of 583 mAh g-1 (Li6PS5Cl contribution: 379 mAh g-1) at 0.1 C, a high areal capacity of 3.84 mAh cm-2, and good cycling stability at an operation temperature of 25 °C. These findings highlight the potential of bifunctional organic electrode materials in sulfide-based all-solid-state batteries to overcome the key challenges of organic electrode materials in practical applications.





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