Constructing thick electrodes with high Li+ adsorption capacity and excellent kinetic performance effectively addresses the low efficiency of lithium extraction from salt lake brines. However, an increase in the content of active material can hinder the Li+ mass transfer within the electrode, resulting in polarization and reduced kinetic performance, which ultimately affects the extraction efficiency. This study synthesized a three-dimensional(3D) conductive network-incorporated thick electrode (∼20 mg/cm2) composed of the redox graphene oxide-loaded LFP(LFP/rGO) composite through an in situ hydrothermal method. The electrode material showed excellent kinetic performance and a high adsorption capacity for Li+ in salt lake brine. Under a constant voltage of 0.8 V in Li+ solution, the Li+ adsorption capacity reached 36.78 mg·g−1 within 10 min, exhibiting an average coulombic efficiency of over 83.53 %. Furthermore, the LFP/rGO composite thick electrode exhibited a Li+ adsorption capacity of 32.82 mg·g−1, along with an average coulombic efficiency of 74.6 %, even in the West Taijinar old brine solution. Additionally, the electrode material demonstrated remarkable cycling stability, maintaining a capacity of 172.09 mAh·g−1 after 50 cycles at a 0.2C rate in a high-concentration salt lake brine. Our preparation strategy offers novel insights for high-performance lithium extraction electrodes.@en

Enhancing the kinetic performance of thick electrodes is essential for improving the efficiency of lithium extraction processes. Biochar, known for its affordability and unique three-dimensional (3D) structure, is utilized across various applications. In this study, we developed a biochar-based, 3D-conductive network thick electrode (∼20 mg cm−2) by in-situ deposition of LiFePO4 (LFP) onto watermelon peel biomass (WB). Utilizing Density Functional Theory (DFT) calculations complemented by experimental data, we confirmed that this The thick electrode exhibits outstanding kinetic properties and a high capacity for lithium intercalation in brines, even in environments where the Magnesia-lithium ratios are significantly high. The electrode showed an impressive intercalation capacity of 30.67 mg g−1 within 10 min in a pure lithium solution. It also maintained high intercalation performance (31.17 mg g−1) in simulated brines with high Magnesia-lithium ratios. Moreover, in actual brine, it demonstrated a significant extraction capacity (23.87 mg g−1), effectively lowering the Magnesia-lithium ratio from 65 to 0.50. This breakthrough in high-conductivity thick electrode design offers new perspectives for lithium extraction technologies.@en

Improving the kinetic performance of thick electrodes is key to enhancing lithium extraction from salt lakes. Nano-melamine foam (MF), known for its unique porous structure, is ideal for building a three-dimensional (3D) conductive network, thereby boosting electrode kinetics. In our study, we developed a thick electrode (20 mg·g−1) with a 3D-conductive network by in-situ growing LiFePO4 (LFP) onto a nanoscale MF substrate. This electrode exhibited superior kinetic performance and a high lithium adsorption capacity in brine, achieving up to 32.8 mg·g−1 in just 10 min. Remarkably, even in simulated brine with a high Mg2+/Li+ ratio, it maintained an average coulomb efficiency of 62 %, significantly lowering the Mg2+/Li+ ratio from 65.6 to 0.47. It also showed exceptional stability in actual brine, maintaining an average coulomb efficiency of about 56.6 %. Our development of this high conductivity, thick electrode provides new insights into efficient lithium extraction methods.@en