Journal of Energy Storage, Год журнала: 2024, Номер 103, С. 114389 - 114389
Опубликована: Ноя. 1, 2024
Язык: Английский
Journal of Energy Storage, Год журнала: 2024, Номер 103, С. 114389 - 114389
Опубликована: Ноя. 1, 2024
Язык: Английский
Advanced Materials, Год журнала: 2024, Номер unknown
Опубликована: Сен. 30, 2024
Abstract Oxygen electrocatalysis, as the pivotal circle of many green energy technologies, sets off a worldwide research boom in full swing, while its large kinetic obstacles require remarkable catalysts to break through. Here, based on summarizing reaction mechanisms and situ characterizations, structure–activity relationships oxygen electrocatalysts are emphatically overviewed, including influence geometric morphology chemical structures electrocatalytic performances. Subsequently, experimental/theoretical is combined with device applications comprehensively summarize cutting‐edge according various material categories. Finally, future challenges forecasted from perspective catalyst development applications, favoring researchers promote industrialization electrocatalysis at an early date.
Язык: Английский
Процитировано
16Advanced Composites and Hybrid Materials, Год журнала: 2025, Номер 8(1)
Опубликована: Янв. 24, 2025
Язык: Английский
Процитировано
4Advanced Functional Materials, Год журнала: 2025, Номер unknown
Опубликована: Фев. 2, 2025
Abstract The structural instability of lithium‐based transition metal layered oxides during electrochemical cycling‐exacerbated by phenomena such as dissolution and phase transitions‐induces rapid capacity degradation, thus constraining their applicability in high‐energy‐density lithium batteries. While coating these materials can bolster stability, the employment electrochemically inactive coatings may inadvertently undermine energy storage performance, presenting a significant trade‐off. In response to this challenge, an innovative core‐shell cathode architecture is presented, wherein high entropy doped LiNi 1/6 Mn Al Ti Mo Ta O 2 serves shell nickel‐rich cobalt‐free 0.89 0.11 constitutes core, synthesized through simple two‐step co‐precipitation methodology (designated LHECNM). This high‐entropy preserves core's performance while effectively mitigating transformations ion dissolution, thereby enhancing robustness. Moreover, configuration significantly diminishes barrier for Li + diffusion, facilitating superior transport dynamics. Consequently, LHECNM demonstrates remarkable achieving discharge 201.57 mAh g −1 , commendable rate capability up 5C, impressive 92% retention over prolonged cycling. investigation elucidates promising paradigm design materials, offering profound insights advancement future technologies.
Язык: Английский
Процитировано
2Advanced Functional Materials, Год журнала: 2024, Номер unknown
Опубликована: Ноя. 5, 2024
Abstract Unraveling the fundamental mechanisms of sodium ion adsorption behavior is crucial for guiding design electrode materials and enhancing performance capacitive deionization systems. Herein, optimization systematically investigated through robust d–d orbital interactions within zinc‐doped iron carbide, facilitated by a novel liquid nitrogen quenching treatment. Liquid treatment can enhance coordination number, strengthen interactions, promote electron transfer, shift d‐band center Fe closer to Fermi level, thereby ions energy. Consequently, obtained material achieves superior gravimetric capacity 121.1 mg g −1 attractive cyclic durability. The highly competitive compared vast majority related research works in field deionization. Furthermore, adsorption/desorption are substantiated ex situ techniques, revealing dynamic atomic electronic structure evolutions under operational conditions. This work demonstrates that optimizing via modulation enabled an effective approach developing efficient materials.
Язык: Английский
Процитировано
5Applied Catalysis B Environment and Energy, Год журнала: 2024, Номер 358, С. 124435 - 124435
Опубликована: Июль 26, 2024
Язык: Английский
Процитировано
4Chemical Engineering Journal, Год журнала: 2024, Номер unknown, С. 158196 - 158196
Опубликована: Дек. 1, 2024
Язык: Английский
Процитировано
4Journal of Colloid and Interface Science, Год журнала: 2025, Номер 683, С. 995 - 1002
Опубликована: Янв. 2, 2025
Язык: Английский
Процитировано
0Journal of Alloys and Compounds, Год журнала: 2025, Номер unknown, С. 178578 - 178578
Опубликована: Янв. 1, 2025
Язык: Английский
Процитировано
0ACS Catalysis, Год журнала: 2025, Номер 15(3), С. 1607 - 1615
Опубликована: Янв. 15, 2025
Efficiently converting methane (CH4) to C1 products such as CH3OH, HCHO, and CH3OOH is considered a promising route for the chemical industry, while huge challenge of low CH4 activation rate still remains. Here, Cu/ZnO composite catalyst with CuOx supported on ZnO synthesized modify electronic structure utilized conversion. The fast e– transfer channel → Cu O2 facilitates dissociation •OOH, which promotes charge separation and, in parallel, enables oxidation •CH3 by h+ left acceleration effect situ generated •OOH. Mechanistic studies revealed that additional d-π*/d-σ-orbital hybridization between adsorbed O2/CH4 molecules plays decisive roles activation, resulted highest signal, so far we know, ultimately remarkably high yield 21.25 mmol g–1 h–1 100% selectivity over optimized 1 wt % photocatalyst. This work offers valuable guidance designation conversion presence O2.
Язык: Английский
Процитировано
0Advanced Composites and Hybrid Materials, Год журнала: 2025, Номер 8(1)
Опубликована: Янв. 20, 2025
Язык: Английский
Процитировано
0