Eco-friendly utilization of sawdust: Ionic liquid-modified biochar for enhanced Li+ storage of TiO2
Creators
- 1. College of Biology and the Environment, Nanjing Forestry University, 159 Longpan Road, Nanjing 210037 (China)
- 2. Institute of Chemical Industry of Forestry Products, Chinese Academy of Forestry, 16 Suojin Wucun, Nanjing 210042 (China)
- 3. Ningbo Institute of Materials Technology and Engineering, Chinese Academy of Sciences, Zhongguan West Road, Ningbo 315201 (China)
Description
Highlights: • Sawdust modified by [Bmim]H2PO4 converted into high performance anodes. • N-O-Ti/N-Ti-O and P-O-Ti bonds in biochar/TiO2 interface detected by XPS. • Biochar/TiO2 interface bonding enhanced anodic structural/cyclic stability. • IL-assisted low-temperature carbonization is environmental-friendly. In China, forestry logging and wood processing produce hundreds of thousands of tons of sawdust every year, which is either discarded or burned. These nonecofriendly practices result in some challenges associated with greenhouse gas emissions. Sawdust-based biochar tailored for anodes of lithium-ion batteries (LIBs) can effectively realize value-added utilization of sawdust. The purpose of the current work is to prepare TiO2/biochar nanocomposites to improve the electrical conductivity and structural stability of the anode. However, poor interfacial interaction between TiO2 and carbon in the TiO2/C composites arising from their heterogeneous nature leads to structural deformation of the composites used as anodes of lithium-ion batteries (LIBs). A strategy of constructing ionic liquid-coupled biochar/TiO2 interfaces is proposed to obtain chemically bonded interfaces between TiO2 and sawdust-derived biochar. In this study, TiO2/C-880 composites are prepared by one-step carbonization of TiO2 nanoparticles (NPs) and sawdust at 880 °C previously dissolved in 1-butyl-3-methyl-imidazolium ([Bmim]H2PO4)/dimethyl sulfoxide (DMSO). The morphologies of TiO2/C-880 demonstrate that the TiO2 is encapsulated by porous biochar with intimate interfaces, and the X-ray photoelectron spectroscopy (XPS) results indicate the formation of N-Ti-O/N-O-Ti and Ti-O-P bonds that bridge the two components. TiO2/C-880 electrodes have high reversible specific capacities (404 mAh g−1 at 0.1 A g−1) and desirable long-term cyclic stability (100 mAh g−1 at 2 A g−1 throughout 2500 cycles). Moreover, large diffusion coefficients (DLi+) ranging from 5.9 × 10−11 to 1.2 × 10−9 cm2 s−1 are obtained from galvanostatic intermittent titration (GITT) curves. The N-Ti-O/N-O-Ti and Ti-O-P bonds at the interfaces offer routes for fast Li+/electron transport, which account for the high performance of the TiO2/C-880 electrodes.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.scitotenv.2021.148688Additional details
Identifiers
- DOI
- 10.1016/j.scitotenv.2021.148688;
- PII
- S0048969721037608;
Publishing Information
- Journal Title
- Science of the Total Environment
- Journal Volume
- 794
- Journal Page Range
- vp.
- ISSN
- 0048-9697
- CODEN
- STENDL
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 54054063
- Subject category
- S36: MATERIALS SCIENCE; S77: NANOSCIENCE AND NANOTECHNOLOGY;
- Descriptors DEI
- ANODES; CARBONIZATION; CHARCOAL; DMSO; ELECTRIC CONDUCTIVITY; GREENHOUSE GASES; LITHIUM ION BATTERIES; LITHIUM IONS; MORPHOLOGY; NANOCOMPOSITES; NANOPARTICLES; POROUS MATERIALS; TITANIUM OXIDES; TITRATION; X-RAY PHOTOELECTRON SPECTROSCOPY
- Descriptors DEC
- ADSORBENTS; CHALCOGENIDES; CHARGED PARTICLES; CHEMICAL ANALYSIS; CHEMICAL REACTIONS; DECOMPOSITION; ELECTRIC BATTERIES; ELECTRICAL PROPERTIES; ELECTROCHEMICAL CELLS; ELECTRODES; ELECTRON SPECTROSCOPY; ENERGY STORAGE SYSTEMS; ENERGY SYSTEMS; IONS; MATERIALS; NANOMATERIALS; ORGANIC COMPOUNDS; ORGANIC SULFUR COMPOUNDS; OXIDES; OXYGEN COMPOUNDS; PARTICLES; PHOTOELECTRON SPECTROSCOPY; PHYSICAL PROPERTIES; QUANTITATIVE CHEMICAL ANALYSIS; SPECTROSCOPY; SULFOXIDES; TITANIUM COMPOUNDS; TRANSITION ELEMENT COMPOUNDS; VOLUMETRIC ANALYSIS
Optional Information
- Copyright
- Copyright (c) 2021 Elsevier B.V. All rights reserved.