RESUMEN

The utilization of biomass pyrolysis is a crucial approach for sustainable development. This study used the typical biomass of pine (PI), rice husk (RH), and corn straw (ST) as feedstocks to evaluate the pyrolysis mechanisms, features and conversion mechanisms of the phenol tar product. The phenolic gaseous products were more trailing in ST, which mostly concentrated around 320-500 °C. Primary phenol tar is produced from lignin through the homolytic cleavage of ß-O and α-O, and C-C bond breakage, primarily occurring before 550 °C. As the degree of aromatization increases, the oxygenates progressively deoxygenate, and the primary tar demethoxylates to form secondary tar as the temperature increases. The pyrolysis of cellulose produces H radicals, which aid the transformation of lignin into phenol tar. This study can provide a theoretical basis for biomass pyrolysis to select the appropriate process parameters to improve the quality of bio-oil and regulate phenol tar products.

Asunto(s)

Biomasa , Lignina , Pirólisis , Lignina/química , Breas/química , Fenol/química , Fenoles/química , Zea mays/química , Oryza/química , Pinus/química , Temperatura

RESUMEN

Recently, aqueous Zn-X (X=S, Se, Te, I2, Br2) batteries (ZXBs) have attracted extensive attention in large-scale energy storage techniques due to their ultrahigh theoretical capacity and environmental friendliness. To date, despite tremendous research efforts, achieving high energy density in ZXBs remains challenging and requires a synergy of multiple factors including cathode materials, reaction mechanisms, electrodes and electrolytes. In this review, we comprehensively summarize the various reaction conversion mechanism of zinc-sulfur (Zn-S) batteries, zinc-selenium (Zn-Se) batteries, zinc-tellurium (Zn-Te) batteries, zinc-iodine (Zn-I2) batteries, and zinc-bromine (Zn-Br2) batteries, along with recent important progress in the design and electrolyte of advanced cathode (S, Se, Te, I2, Br2) materials. Additionally, we investigate the fundamental questions of ZXBs and highlight the correlation between electrolyte design and battery performance. This review will stimulate an in-deep understanding of ZXBs and guide the design of conversion batteries.

RESUMEN

Zinc ion batteries (ZIBs), generally established on an excessive metallic Zn anode and aqueous electrolytes, suffer from severe dendrites and gassing issues at Zn side, resulting in poor cycling life. Substituting Zn metal anode with non-Zn ones is a promising strategy for solving these problems, whereas this is still restricted by the limited anode alternatives. Herein, by replacing metal Zn with chalcogen element tellurium (Te), a conversion-type Te-based ZIB is reported that can work in both mild and alkaline electrolytes. As expected, the as-assembled mild Te/MnO2 and alkaline Te/Ni(OH)2 cells deliver remarkable capacities up to 106 and 161 mAh g-1 anode+cathode , respectively, with a high utilization of anode (50.1% for the Te/MnO2 and 38.9% for the Te/Ni(OH)2 ), which surpass all ZIBs. Ultralong cycling life (over 75% capacity retention after 5000 cycles) is achieved in the two systems, benefiting from the stable conversion mechanisms (mild: Te to ZnTe2 to ZnTe; alkaline: ZnTe to Te to TeO2 ) with thoroughly eliminated dendrites and gassing. Moreover, high gravimetric energy density of ZIBs is also achieved, which are 176.3 Wh kg-1 anode+cathdoe (Te/Ni(OH)2 ) and 81 Wh Kg-1 anode+cathode (Te/MnO2 ), respectively. This work sheds light on the development of advanced conversion-type anode for high-performance batteries with superior stability.

RESUMEN

Owing to their high specific capacity and abundant reserve, Cux S compounds are promising electrode materials for lithium-ion batteries (LIBs). Carbon compositing could stabilize the Cux S structure and repress capacity fading during the electrochemical cycling, but the corresponding Li+ storage mechanism and stabilization effect should be further clarified. In this study, nanoscale Cu2 S was synthesized by CuS co-precipitation and thermal reduction with polyelectrolytes. High-temperature synchrotron radiation diffraction was used to monitor the thermal reduction process. During the first cycle, the conversion mechanism upon lithium storage in the Cu2 S/carbon was elucidated by operando synchrotron radiation diffraction and in situ X-ray absorption spectroscopy. The N-doped carbon-composited Cu2 S (Cu2 S/C) exhibits an initial discharge capacity of 425 mAh g-1 at 0.1 A g-1 , with a higher, long-term capacity of 523 mAh g-1 at 0.1 A g-1 after 200 cycles; in contrast, the bare CuS electrode exhibits 123 mAh g-1 after 200 cycles. Multiple-scan cyclic voltammetry proves that extra Li+ storage can mainly be ascribed to the contribution of the capacitive storage.

RESUMEN

The increase in energy density of the next generation of battery materials to meet the new challenges of the electrical vehicles era calls for innovative and easily scalable materials with sustainable processes. An innovative Cu x O/C nanocomposite material, characterized by a highly conductive 3D-framework, with Cu x O/Cu-metal contiguous nanodomains is prepared by electrospinning. The electrode processing is made using a polyacrylic acid binder. The nanocomposite has been fully characterized and the electrochemical performance shows high specific capacity values over 450 galvanostatic cycles at 500 mAg-1 specific current with capacity retention values over 80 %. In addition, the composite shows remarkable high rate performance and highly stable interface, which has been studied by impedance spectroscopy.

RESUMEN

Hollow materials derived from metal-organic frameworks (MOFs), by virtue of their controllable configuration, composition, porosity, and specific surface area, have shown fascinating physicochemical properties and widespread applications, especially in electrochemical energy storage and conversion. Here, the recent advances in the controllable synthesis are discussed, mainly focusing on the conversion mechanisms from MOFs to hollow-structured materials. The synthetic strategies of MOF-derived hollow-structured materials are broadly sorted into two categories: the controllable synthesis of hollow MOFs and subsequent pyrolysis into functional materials, and the controllable conversion of solid MOFs with predesigned composition and morphology into hollow structures. Based on the formation processes of hollow MOFs and the conversion processes of solid MOFs, the synthetic strategies are further conceptually grouped into six categories: template-mediated assembly, stepped dissolution-regrowth, selective chemical etching, interfacial ion exchange, heterogeneous contraction, and self-catalytic pyrolysis. By analyzing and discussing 14 types of reaction processes in detail, a systematic mechanism of conversion from MOFs to hollow-structured materials is exhibited. Afterward, the applications of these hollow structures as electrode materials for lithium-ion batteries, hybrid supercapacitors, and electrocatalysis are presented. Finally, an outlook on the emergent challenges and future developments in terms of their controllable fabrications and electrochemical applications is further discussed.