Facile Synthesis of Sustainable Activated Biochars with Different Pore Structures as Efficient Additive-Carbon-Free Anodes for Lithium- and Sodium-Ion Batteries

生物炭 阳极 锂(药物) 碳纤维 电化学 介孔材料 材料科学 吸附 化学工程 活性炭 化学 热解 无机化学 电极 催化作用 有机化学 复合数 复合材料 冶金 物理化学 内分泌学 工程类 医学
作者
Glaydson S. dos Reis,Chandrasekar Mayandi Subramaniyam,Angélica Duarte Cárdenas,Sylvia H. Larsson,Mikael Thyrel,Ulla Lassi,F. Garcı́a-Alvarado
出处
期刊:ACS omega [American Chemical Society]
卷期号:7 (46): 42570-42581 被引量:9
标识
DOI:10.1021/acsomega.2c06054
摘要

The present work elucidates facile one-pot synthesis from biomass forestry waste (Norway spruce bark) and its chemical activation yielding high specific surface area (SBET) biochars as efficient lithium- and sodium-ion storage anodes. The chemically activated biochar using ZnCl2 (Biochar-1) produced a highly mesoporous carbon containing 96.1% mesopores in its structure as compared to only 56.1% mesoporosity from KOH-activated biochars (Biochar-2). The latter exhibited a lower degree of graphitization with disordered and defective carbon structures, while the former presented more formation of ordered graphite sheets in its structure as analyzed from Raman spectra. In addition, both biochars presented a high degree of functionalities on their surfaces but Biochar-1 presented a pyridinic-nitrogen group, which helps improve its electrochemical response. When tested electrochemically, Biochar-1 showed an excellent rate capability and the longest capacity retentions of 370 mA h g–1 at 100 mA g–1 (100 cycles), 332.4 mA h g–1 at 500 mA g–1 (1000 cycles), and 319 mA h g–1 at 1000 mA g–1 after 5000 cycles, rendering as an alternative biomass anode for lithium-ion batteries (LIBs). Moreover, as a negative electrode in sodium-ion batteries, Biochar-1 delivered discharge capacities of 147.7 mA h g–1 at 50 mA g–1 (140 cycles) and 126 mA h g–1 at 100 mA g–1 after 440 cycles.
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