Journal of Alloys and Compounds, Год журнала: 2024, Номер unknown, С. 177834 - 177834
Опубликована: Ноя. 1, 2024
Язык: Английский
Journal of Alloys and Compounds, Год журнала: 2024, Номер unknown, С. 177834 - 177834
Опубликована: Ноя. 1, 2024
Язык: Английский
Energy Materials, Год журнала: 2024, Номер 4(6)
Опубликована: Ноя. 8, 2024
The rechargeable alkali metal-ion batteries (RAMIBs) are highly promising candidates for next-generation efficient energy storage devices, owing to their outstanding theoretical specific capacities and extremely low electrochemical potentials. However, RAMIBs possess unsuitable lifespans, mechanical durability inevitable side reactions attributable inherent severe volumetric/structure alteration during the charge-discharge cycles. These hitches could be solved using porous multimetallic alloy-based anodes, due impressive capacities, working potential, cost, earth-abundance, which can meet sustainability practical application needs. Meanwhile, great surface area, electrical conductivity, structural stability, ability accommodate generated metal ions yield satisfactory coulomb efficiency long durability. Immense efforts dedicated rationally designing anodes RAMIBs, so it is essential provide timely updates on this research area. Herein, we reviewed recent advances in (i.e., Sn, Mn, Mo, Co, V, Fe) lithium-ion batteries, sodium-ion potassium-ion batteries. This rooted engineering approaches template-based, hydrothermal/solvothermal, chemical reduction, deposition, sol-gel, electrospinning) fundamental insights mechanisms, key parameters, calculations) precise evaluation changes, mechanisms by various experimental, theoretical, in-situ analysis optimizing performance. Also, recycling circular economy were discussed. Eventually, highlighted current drawbacks provided proposed perspectives solve these issues enable utilization of such large-scale applications.
Язык: Английский
Процитировано
3Journal of Power Sources, Год журнала: 2025, Номер 641, С. 236812 - 236812
Опубликована: Март 21, 2025
Язык: Английский
Процитировано
0ChemistrySelect, Год журнала: 2025, Номер 10(13)
Опубликована: Апрель 1, 2025
Abstract To investigate the potential of MXene‐catalyzed electroreduction carbon dioxide towards achieving highly efficient ECO 2 RR, this study engineered an S ‐anchoring site on Ti 3 C T x MXene for Zn ion coordination. The findings revealed that was uniformly distributed across surface and interface, either replacing or integrating with functional groups, effectively coordinating Zn. Subsequently, nanoparticles were synthesized leveraging defect‐induced self‐reduction capability support. presence facilitated rapid electron transfer to Zn, accelerated activation dioxide, endowed Zn‐S‐MXene a larger active area, enhanced RR selectivity, faster charge rate. Consequently, CO selectivity significantly enhanced, reaching impressive FE 89.7%. This offers novel perspectives utilization atomic modifications in materials design optimization through strategic pairing metal ions.
Язык: Английский
Процитировано
0Advanced Materials, Год журнала: 2025, Номер unknown
Опубликована: Май 19, 2025
Abstract The trade‐off of the Volmer reaction for *H formation and Heyrovsky/Tafel Reaction desorption is a crucial challenge in alkaline hydrogen evolution (HER). Thus, aside from conventional construction bifunctional active sites to accelerate water dissociation step, electronic retrimming each metal site also non‐negligible. Herein, an efficient HER electrocatalyst combining Pt single‐atoms nanoparticles on etched boron nitride (eBN) coated carbon nanotube (Pt‐eBN@CNT) synthesized, where both Heyrovsky steps are promoted by synergistic adsorption composite electron‐withdrawing effect eBN carrier, respectively. proposed catalyst shows impressive performance media with overpotential 25.1 ± 1.7 mV at 10 mA cm −2 , TOF 17.1 1.3 s −1 0.15 V vs RHE under extremely low loading 6 µg (catalyst 0.77 mg ), significantly better than those commercial benchmark Pt/C (44.2 4.1 mV, 0.9 0.1 ; 156.1 0.6 1.6 ) same conditions. Moreover, membrane‐electrode‐assembly (MEA) electrolyzer Pt‐eBN@CNT as cathodic exhibits notable charge transfer amount (stands long service life) 2.0 × C·cm within high‐temperature electrocatalysis 1.0 A·cm higher state‐of‐the‐art Pt‐based electrocatalysts. This work demonstrates important role active‐site combination coupled carrier optimizing kinetics multi‐step electrocatalytic reaction.
Язык: Английский
Процитировано
0Dalton Transactions, Год журнала: 2024, Номер 53(20), С. 8563 - 8575
Опубликована: Янв. 1, 2024
The Oxygen Evolution Reaction (OER) is crucial in various processes such as hydrogen production
Язык: Английский
Процитировано
2CHINESE JOURNAL OF CATALYSIS (CHINESE VERSION), Год журнала: 2024, Номер 62, С. 53 - 107
Опубликована: Июль 1, 2024
Язык: Английский
Процитировано
2Nanoscale, Год журнала: 2024, Номер 16(15), С. 7467 - 7479
Опубликована: Янв. 1, 2024
Elevated temperature-driven pyrolysis can generate coordinatively unsaturated NiSA-NC-900, crucial for the oxygen evolution process in water splitting, through coordination rebuilding and N-loss processes.
Язык: Английский
Процитировано
1Inorganic Chemistry Frontiers, Год журнала: 2024, Номер 11(18), С. 5884 - 5893
Опубликована: Янв. 1, 2024
Benefiting from the metal-support interactions, prepared Ru-NiCoO 2 /CC exhibits excellent alkaline HER activity. Importantly, two-electrode electrolyzer with demonstrates potential for integration intermittent energy systems.
Язык: Английский
Процитировано
1Journal of Colloid and Interface Science, Год журнала: 2024, Номер 678, С. 1223 - 1229
Опубликована: Сен. 23, 2024
Язык: Английский
Процитировано
1Inorganic Chemistry, Год журнала: 2024, Номер 63(33), С. 15477 - 15484
Опубликована: Авг. 6, 2024
Transition-metal phosphides (TMPs) have attracted extensive attention in energy-related fields, especially for electrocatalytic hydrogen evolution reaction (HER). However, it is imperative to develop a facile and time-consuming approach prepare metal with satisfactory catalytic performance. Herein, nitrogen-doped CoP-Co
Язык: Английский
Процитировано
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