“…After the first CV cycle, the observed reduction peaks during the first cycle appeared around 1.86 and 0.742 V were shifted to 1.87 and 0.73 V, and the oxidation peaks at 0.992 and 2.05 V were shifted to 1.01 and 2.04 V, respectively. The shifts in the redox peaks during the later cycles could be ascribed to the improved diffusion kinetics of Li ions . Notably, the redox peaks exhibit identical shape and position during the second and third cycles, which implies the excellent cycling stability of the NiS 2 :Mo electrode …”
Section: Resultsmentioning
confidence: 92%
“…In the following first anodic scan, an intense peak appeared at 0.992 V and two less intense peaks appeared around 1.35 and 2.05 V ( vs Li + /Li). The peak appeared at 0.992 V is related to the partial dissolution of the SEI film . On the other hand, the peak appeared around 2.05 V is associated with the delithiation of Li + and oxidation of metallic Ni and formation of NiS 2 , and the peak appeared around 1.35 V corresponds to the oxidation of Mo to form MoO 3 .…”
Section: Resultsmentioning
confidence: 96%
“…One successful approach to tackle these issues of anode materials is the doping TMOs/TMSs with metal ions. Several mono- and multivalent dopant ions, such as Cu 2+ ,Co 2+ , Mo 6+ , Nb 5+ , Cr 3+ , Ti 4+ , etc., were used to dope TMOs/TMSs and tested as anode materials for LIBs. ,− Among the tested dopants, Mo was seen to improve the specific capacity and cycling stability of TMO/TMS electrodes remarkably. , For instance, Chen et al showed that doping of porous WO 2 with Mo stabilizes its structure and improves its electronic conductivity, resulting in its performance enhancement as the electrode material in LIBs. Recently, we have shown that Mo doping in Cu 2 O-based anodes can substantially enhance its specific capacity (up to 1128 mAh g –1 at 0.1 Ag –1 ) and cycling stability in LIBs .…”
Transition-metal
sulfides (TMSs) are promising anode materials
for lithium-ion batteries (LIBs) as they exhibit anomalously high
specific capacities. However, the electrodes made on TMSs possess
low electronic conductivity and poor specific capacity retention,
which hinder their application in LIBs. Herein, we report a one-step,
simple, hydrothermal technique for synthesizing molybdenum-doped nickel
disulfide (NiS2:Mo) microspheres with varying Mo contents
(0, 5, and 10 wt %) and their performance as anode materials in LIBs.
Mo doping was found to improve the electronic conductivity, structural
stability, and reduce charge transfer resistance between the electrode/electrolyte
interface of NiS2 microspheres, thereby achieving a superior
electrochemical performance in LIBs. The anode made of NiS2:Mo microspheres with 5 wt % Mo registered a maximum specific capacity
and cycling durability. It delivered an outstanding initial specific
capacity of 1605 mAh g–1 at 0.1 Ag–1 and exhibited exceptional cycling stability with a reversible discharge
capacity retention of 713.3 mAh g–1 after 120 cycles
and Coulombic efficiency of 98.42%. Such exceptionally high specific
capacity and high charge–discharge capacity retention of the
NiS2:Mo (5%) microspheres indicate that the material is
a promising anode material for LIBs and other advanced energy storage
applications.
“…After the first CV cycle, the observed reduction peaks during the first cycle appeared around 1.86 and 0.742 V were shifted to 1.87 and 0.73 V, and the oxidation peaks at 0.992 and 2.05 V were shifted to 1.01 and 2.04 V, respectively. The shifts in the redox peaks during the later cycles could be ascribed to the improved diffusion kinetics of Li ions . Notably, the redox peaks exhibit identical shape and position during the second and third cycles, which implies the excellent cycling stability of the NiS 2 :Mo electrode …”
Section: Resultsmentioning
confidence: 92%
“…In the following first anodic scan, an intense peak appeared at 0.992 V and two less intense peaks appeared around 1.35 and 2.05 V ( vs Li + /Li). The peak appeared at 0.992 V is related to the partial dissolution of the SEI film . On the other hand, the peak appeared around 2.05 V is associated with the delithiation of Li + and oxidation of metallic Ni and formation of NiS 2 , and the peak appeared around 1.35 V corresponds to the oxidation of Mo to form MoO 3 .…”
Section: Resultsmentioning
confidence: 96%
“…One successful approach to tackle these issues of anode materials is the doping TMOs/TMSs with metal ions. Several mono- and multivalent dopant ions, such as Cu 2+ ,Co 2+ , Mo 6+ , Nb 5+ , Cr 3+ , Ti 4+ , etc., were used to dope TMOs/TMSs and tested as anode materials for LIBs. ,− Among the tested dopants, Mo was seen to improve the specific capacity and cycling stability of TMO/TMS electrodes remarkably. , For instance, Chen et al showed that doping of porous WO 2 with Mo stabilizes its structure and improves its electronic conductivity, resulting in its performance enhancement as the electrode material in LIBs. Recently, we have shown that Mo doping in Cu 2 O-based anodes can substantially enhance its specific capacity (up to 1128 mAh g –1 at 0.1 Ag –1 ) and cycling stability in LIBs .…”
Transition-metal
sulfides (TMSs) are promising anode materials
for lithium-ion batteries (LIBs) as they exhibit anomalously high
specific capacities. However, the electrodes made on TMSs possess
low electronic conductivity and poor specific capacity retention,
which hinder their application in LIBs. Herein, we report a one-step,
simple, hydrothermal technique for synthesizing molybdenum-doped nickel
disulfide (NiS2:Mo) microspheres with varying Mo contents
(0, 5, and 10 wt %) and their performance as anode materials in LIBs.
Mo doping was found to improve the electronic conductivity, structural
stability, and reduce charge transfer resistance between the electrode/electrolyte
interface of NiS2 microspheres, thereby achieving a superior
electrochemical performance in LIBs. The anode made of NiS2:Mo microspheres with 5 wt % Mo registered a maximum specific capacity
and cycling durability. It delivered an outstanding initial specific
capacity of 1605 mAh g–1 at 0.1 Ag–1 and exhibited exceptional cycling stability with a reversible discharge
capacity retention of 713.3 mAh g–1 after 120 cycles
and Coulombic efficiency of 98.42%. Such exceptionally high specific
capacity and high charge–discharge capacity retention of the
NiS2:Mo (5%) microspheres indicate that the material is
a promising anode material for LIBs and other advanced energy storage
applications.
“…50,56 Last, the transition metals may play the role of a catalyst, leading to electrolyte decomposition during the delithiation process, thus providing some additional capacities. 35,62 The NiS@C and pure-NiS, by contrast, only exhibit the capacities of 405.5 and 63.6 mA h g −1 after 1500 cycles at 1 A g −1 with a lower capacity retention of 76.7% and 14.9%, respectively. The above results further demonstrate that the proper recombination of Cu 2 S and the construction of the S/N co-doped carbon coating structure is an effective strategy to improve the lithium storage performance of the NiS.…”
Section: Resultsmentioning
confidence: 99%
“…Cu 2+ and Ni 3+ co-doped Ni(OH) 2 (Cu-Ni(OH) 2 ) and Pure-Ni(OH) 2 were synthesized through a simple co-precipitation method which can be found in our previous research. 35 For the preparation of N/S co-doped carbon-coated NiS/Cu 2 S (NiS/ Cu 2 S@N/S-C), typically, 0.5 g as-synthesized Cu-Ni(OH) 2 and 0.5 g dopamine hydrochloride (PDA) were firstly dispersed into 0.5 L Tris buffer solution ( pH = 8.5). After stirring for 24 h at 25 °C, the black precipitate product was obtained through filtering the above mixture.…”
Nickel sulfides are promising anode materials for lithium-ion batteries (LIBs) due to their high theoretical capacities but suffer from the sluggish kinetic process and poor structural stability. Herein, we develop...
Rh has been widely studied as a catalyst for the promising hydrazine oxidation reaction that can replace oxygen evolution reactions for boosting hydrogen production from hydrazine‐containing wastewater. Despite Rh being expensive, only a few studies have examined its electrocatalytic mass activity. Herein, surface‐limited cation exchange and electrochemical activation processes are designed to remarkably enhance the mass activity of Rh. Rh atoms were readily replaced at the Ni sites on the surface of NiOOH electrodes by cation exchange, and the resulting RhOOH compounds were activated by the electrochemical reduction process. The cation exchange‐derived Rh catalysts exhibited particle sizes not exceeding 2 nm without agglomeration, indicating a decrease in the number of inactive inner Rh atoms. Consequently, an improved mass activity of 30 A mgRh−1 was achieved at 0.4 V versus reversible hydrogen electrode. Furthermore, the two‐electrode system employing the same CE‐derived Rh electrodes achieved overall hydrazine splitting over 36 h at a stable low voltage. The proposed surface‐limited CE process is an effective method for reducing inactive atoms of expensive noble metal catalysts.
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