Hybrid supercapacitors using metal-organic framework derived nickel-sulfur compounds.

HYPOTHESIS: Metal-organic frameworks (MOFs) are highly suitable precursors for supercapacitor electrode materials owing to their high porosity and stable backbone structures that offer several advantages for redox reactions and rapid ion transport. EXPERIMENTS: In this study, a carbon-coated Ni9S8 composite (Ni9S8@C-5) was prepared via sulfuration at 500 ℃ using a spherical Ni-MOF as the sacrificial template. FINDING: The stable carbon skeleton derived from Ni-MOF and positive structure-activity relationship due to the multinuclear Ni9S8 components resulted in a specific capacity of 278.06 mAh·g-1 at 1 A·g-1. Additionally, the hybrid supercapacitor (HSC) constructed using Ni9S8@C-5 as the positive electrode and the laboratory-prepared coal pitch-based activated carbon (CTP-AC) as the negative electrode achieved an energy density of 69.32 Wh·kg-1 at a power density of 800.06 W·kg-1, and capacity retention of 83.06 % after 5000 cycles of charging and discharging at 5 A·g-1. The Ni-MOF sacrificial template method proposed in this study effectively addresses the challenges associated with structural collapse and agglomeration of Ni9S8 during electrochemical reactions, thus improving its electrochemical performance. Hence, a simple preparation method is demonstrated, with broad application prospects in supercapacitor electrodes.

Peroxymonosulfate Activation by Facile Fabrication of α-MnO2 for Rhodamine B Degradation: Reaction Kinetics and Mechanism.

The persulfate-based advanced oxidation process has been an effective method for refractory organic pollutants' degradation in aqueous phase. Herein, α-MnO2 with nanowire morphology was facially fabricated via a one-step hydrothermal method and successfully activated peroxymonosulfate (PMS) for Rhodamine B (RhB) degradation. Influencing factors, including the hydrothermal parameter, PMS concentration, α-MnO2 dosage, RhB concentration, initial pH, and anions, were systematically investigated. The corresponding reaction kinetics were further fitted by the pseudo-first-order kinetic. The RhB degradation mechanism via α-MnO2 activating PMS was proposed according to a series of quenching experiments and the UV-vis scanning spectrum. Results showed that α-MnO2 could effectively activate PMS to degrade RhB and has good repeatability. The catalytic RhB degradation reaction was accelerated by increasing the catalyst dosage and the PMS concentration. The effective RhB degradation performance can be attributed to the high content of surface hydroxyl groups and the greater reducibility of α-MnO2, and the contribution of different ROS (reactive oxygen species) was 1O2 > O2·- > SO4·- > ·OH.

Tetrakaidecahedron-shaped Cu four-core supramolecule as novel high-performance electrode material for lithium-ion batteries.

Here, a tetrakaidecahedron-shaped Cu four-core supramolecule was designed to overcome the defects of supramolecules for lithium-ion batteries. With multiple metal centers, conductive ligands and abundant hydrogen bonds, this novel electrode shows excellent rate capability (459.4 mA h g-1 at 2000 mA g-1) and cyclicality (494.5 mA h g-1 after 700 cycles).

Cream roll-inspired advanced MnS/C composite for sodium-ion batteries: encapsulating MnS cream into hollow N,S-co-doped carbon rolls.

With advantages of high theoretical capacity and low cost, manganese sulfide (MnS) has become a potential electrode material for sodium-ion batteries (SIBs). However, complicated preparations and limited cycle life still hinder its application. Inspired by cream rolls in our daily life, a MnS/N,S-co-doped carbon tube (MnS/NSCT) composite with a 3D cross-linked tubular structure is prepared via an ultra-simple and low-cost method in this work. As the anode for SIBs, the cream roll-like MnS/NSCT composite has delivered the best electrochemical performance to date (the highest capacity of 550.6 mA h g-1 at 100 mA g-1, the highest capacity of 447.0 mA h g-1 after 1400 cycles at 1000 mA g-1, and the best rate performance of 319.8 mA h g-1 at 10 000 mA g-1). Besides, according to several in situ and ex situ techniques, the sodium storage mechanism of MnS/NSCTs is mainly from a conversion reaction, and the superior electrochemical performance of MnS/NSCTs is mainly attributed to the unique cream roll-like structure. More importantly, this simple method may be feasible for other anode materials, which will greatly promote the development of SIBs.

Bi-component synergic effect in lily-like CdS/Cu7S4 QDs for dye degradation.

CdS has attracted extensive attention in the photocatalytic degradation of wastewater due to its relatively narrow bandgap and various microstructures. Previous reports have focused on CdS coupled with other semiconductors to reduce the photocorrosion and improve the photocatalytic performance. Herein, a 3D hierarchical CdS/Cu7S4 nanostructure was synthesized by cation exchange using lily-like CdS as template. The heterojunction material completely inherits the special skeleton of the template material and optimizes the nano-scale morphology, and achieves the transformation from nanometer structure to quantum dots (QDs). The introduction of Cu ions not only tuned the band gap of the composites to promote the utilization of solar photons, more importantly, Fenton-like catalysis was combined into the degradation process. Compared with the experiments of organic dye degradation under different illumination conditions, the degradability of the CdS/Cu7S4 QDs is greatly superior to pure CdS. Therefore, the constructed CdS/Cu7S4 QDs further realized the optimization of degradation performance by the synergic effect of photo-catalysis and Fenton-like catalysis.

A Metal-Organic Compound as Cathode Material with Superhigh Capacity Achieved by Reversible Cationic and Anionic Redox Chemistry for High-Energy Sodium-Ion Batteries.

Although sodium-ion batteries (SIBs) are considered as alternatives to lithium-ion batteries (LIBs), the electrochemical performances, in particular the energy density, are much lower than LIBs. A metal-organic compound, cuprous 7,7,8,8-tetracyanoquinodimethane (CuTCNQ), is presented as a new kind of cathode material for SIBs. It consists of both cationic (CuII ↔CuI ) and anionic (TCNQ0 ↔TCNQ- ↔ TCNQ2- ) reversible redox reactions, delivering a discharge capacity as high as 255 mAh g-1 at a current density of 20 mA g-1 . The synergistic effect of both redox-active metal cations and organic anions brings an electrochemical transfer of multiple electrons. The transformation of cupric ions to cuprous ions occurs at near 3.80 V vs. Na+ /Na, while the full reduction of TCNQ0 to TCNQ- happens at 3.00-3.30 V. The remarkably high voltage is attributed to the strong inductive effect of the four cyano groups.

Mechanism of Capacity Fade in Sodium Storage and the Strategies of Improvement for FeS2 Anode.

Pyrite FeS2 has attracted extensive interest as anode material for sodium-ion batteries due to its high capacity, low cost, and abundant resource. However, the micron-sized FeS2 usually suffers from poor cyclability, which stems from structure collapse, exfoliation of active materials, and sulfur dissolution. Here, we use a synergistic approach to enhance the sodium storage performance of the micron-sized FeS2 through voltage control (0.5-3 V), binder choice, and graphene coating. The FeS2 electrode with the synergistic approach exhibits high specific capacity (524 mA h g-1), long cycle life (87.8% capacity retention after 800 cycles), and excellent rate capability (323 mA h g-1 at 5 A g-1). The results prove that a synergistic approach can be applied in the micron-sized sulfides to achieve high electrochemical performance.

Carbon coated K(0.8)Ti(1.73)Li(0.27)O4: a novel anode material for sodium-ion batteries with a long cycle life.

Carbon coated K0.8Ti1.73Li0.27O4 (KTLO) has been synthesized by a facile flux method followed by ball-milling and gaseous carbon coating. The carbon coated KTLO delivers a reversible specific capacity of 119.6 mA h g(-1) at 20 mA g(-1) with no capacity loss after 250 cycles as an anode material in sodium ion batteries, exhibiting an improved rate capability of 66 mA h g(-1) at 200 mA g(-1). It was found that carbon coating of KTLO not only enhances its electronic conductivity, but also improves the structure stability, proving that the carbon coated KTLO is a promising anode material for sodium ion batteries.