Journal of Materials Chemistry A
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2025
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IF 9.5
Wenwen Yin,Jiawei Ma,Yanyan Li,Qing Cheng,Bernt Johannessen,Fangxi Xie,Mingmei Wu
Exploiting bifunctional and highly efficient electrocatalysts that can facilitate the reversible formation and decomposition of discharge products is crucial for rechargeable Na-air batteries (SABs). However, restricted by scaling relations, air cathodes based on single metal systems usually exhibit inferior activity and fail to achieve a stable and long cycle life of Na-air batteries. Dual single-atom catalysts (DACs) with two metal sites can circumvent the scaling relations and endow the single-atom catalysts with superior activity. Herein, we present a hollow carbon microsphere loaded with Ni and Fe single atoms (Ni-HCMs-Fe) as a demonstration of DAC air cathodes for SABs. Notably, Na-air batteries with Ni-HCMs-Fe as an air cathode can achieve a low overpotential gap of 530 mV, a high specific capacity of 5382.9 mAh g−1, and an ultralong cycle life of over 450 cycles (1800 hours) with NaO2 as the main discharge product. Due to the different adsorption energies between oxygenated intermediates and Ni/Fe sites, the Ni-HCMs-Fe catalysts can break through the scaling relations and display optimized binding ability towards intermediates, thus boosting the reversible formation and decomposition of NaO2 in SABs. This work pioneers the use of DACs in SABs, paving the way for their practical applications.
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SEPARATION AND PURIFICATION TECHNOLOGY
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2025
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IF 9
Sifan Bao,Xudong Zheng,Zihuai Xu,Zhouzhou Yang,Wei Sun,Jinfeng Mei,Jian Rong,Zhongyu Li
Carbon aerogel is limited in its application in CO 2 capture due to its poor surface properties. Heteroatom doping is conducive to the adsorption of CO 2 by biochar. Therefore, by in-situ synthesis of nitrogen-doped carbon nanotubes on BC, Ni/N co-doped cellulose carbon aerogel was synthesized, and the results showed excellent adsorption capacity and reversible adsorption/desorption properties. The synthesis of nitrogen-doped carbon nanotubes made the material realize N doping and provided more adsorption sites for CO 2 adsorption. When Ni is dispersed in the material, it not only increases the carbon dioxide adsorption sites but also enhances the thermal stability and cycling performance of the composite material. Meanwhile, the coordination effect between nickel and nitrogen further enhances the capture capacity of carbon dioxide. Ultimately, the adsorption capacity of the modified biochar reached 4.89 mmol/g, and it also has good recycling performance. The unique co-doping design strategy reduces the dependence of traditional carbon materials on surface area when adsorbing CO 2 , providing a new direction for the modification of carbon materials.
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APPLIED CATALYSIS A-GENERAL
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2025
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IF 4.8
Chi Zhang,Junwen Zhang,Lina Che,Xusheng Wang,Li Shi
Photothermal technology offers distinct advantages for catalytic CO 2 methanation. Herein, we synthesized a series of Ni-based catalysts (denoted as TiO 2-x /Ni-X) through controlled calcination of NiTi-layered double hydroxides (LDHs) precursors at 400–700°C. In a continuous-flow system under xenon lamp irradiation (3.2 W/cm²), the TiO 2-x /Ni-X catalysts exhibited a reduction temperature dependent CH 4 production rate. During 40-hour stability testing, the optimized TiO 2-x /Ni-550 catalyst achieved a sustained CH 4 production rate of 180 mmol g cat −1 h −1 with a remarkable near-unity selectivity (>99 %), and the light irradiation substantially enhanced the CH 4 yield compared to bare thermal catalysis. Comprehensive structural characterization and mechanistic studies revealed competing roles governing catalytic activity, with TiO 2-x /Ni-550 demonstrating an optimal balance for CH 4 generation kinetics.
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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
·
2024
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IF 3.8
Shiqiang Wang,Dan Guo,Meng Han,Yitong Yao,Pengfei Zhang,Xuening Zhang,Jing Lv,Yong Wang,Shengping Wang,Xinbin Ma
Syngas, an extremely meaningful chemical feedstock consisting of hydrogen and carbon monoxide, can be produced through methane dry reforming with carbon dioxide. The extensively utilized Ni-based catalysts usually suffer from coke-induced instability. Herein, we design Ni-CeOx bifunctional catalysts with different proximity and explore the influence of proximity level on anticoking performance. Ni-CeOx bimetallic nanoparticles with intimate contact are precisely regulated through the anchoring strategy of coordination unsaturated Al3+penta, which undergoes the topotactic exsolution of a Ni–Ce–O quasi-solid solution into Ni-CeOx bimetallic nanoparticles. A trend toward easier elimination and even the absence of graphitic carbon is observed with a decreasing spatial distance between Ni and CeOx, which is attributed to the proximity between the dissociation and gasification sites of CHx* intermediates. CHx* species generated at Ni nanoparticles migrated to adjacent CeOx oxygen carriers for Ni-CeOx/Al2O3 catalyst gasification with Ni-CeOx bimetallic nanoparticle interfaces, which undergo the Mars–van Krevelen (MvK) mechanism. The exploration of the Ni-CeOx proximity provides guidance for developing efficient and durable Ni-based DRM catalysts.
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Journal of Environmental Chemical Engineering
·
2024
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IF 7.4
Xueqian Wu,Jin Zhao,Jiangyan Tao,Jiawen Chi,Xin Min,Songjian Zhao
As a major greenhouse gas, the rational conversion and utilization of CO 2 can help reduce carbon emissions and mitigate the greenhouse effect. In this study, mesoporous SiO 2 as a carrier, with CuO and NiO employed to construct a binary metal composite silica-based catalyst, coupled with dielectric barrier discharge (DBD) plasma, for the conversion of CO 2 . Physicochemical analysis confirmed the successful introduction of CuO into the mesoporous SiO 2 . NiO and CuO bimetals were dispersed on SiO 2 surfaces with large specific surface areas, ensuring an optimal distribution of metal oxide. Gas chromatography was utilized to investigate the performance of DBD-coupled x%CuO-3 %NiO/Si for CO 2 conversion. The results indicated that the CuO-NiO binary composite silica catalysts significantly improved CO 2 conversion, CO yield, and energy efficiency compared to the monometallic 3 %NiO/Si materials. Further microstructural analysis of the 9 %CuO-3 %NiO/Si catalyst revealed near-elliptic particles with dimensions of 200 by 500 nm and a large number of irregular fine particles attached to the surface. When the CuO loading reached an optimal level and the input power was set at 30 W, the energy efficiency of the 9 %CuO-3 %NiO/Si catalyst increased by 119.6 %. The CuO-NiO binary composite Si-based catalyst developed in this study boasts simple operation and environmental friendliness, making it highly significant for CO 2 treatment.
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Small
·
2024
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IF 13
Yi-Ran Du,Xiao-Qiang Li,Xian-Xia Yang,Guo-Yi Duan,Yong-Mei Chen,Bao-Hua Xu
In this study, the copper-nickel (Cu–Ni) bimetallic electrocatalysts for electrochemical CO 2 reduction reaction(CO 2 RR) are fabricated by taking the finely designed poly(ionic liquids) (PIL) containing abundant Salen and imidazolium chelating sites as the surficial layer, wherein Cu–Ni, PIL–Cu and PIL–Ni interaction can be readily regulated by different synthetic scheme. As a proof of concept, Cu@Salen-PIL@Ni(NO 3 ) 2 and Cu@Salen-PIL(Ni) hybrids differ significantly in the types and distribution of Ni species and Cu species at the surface, thereby delivering distinct Cu–Ni cooperation fashion for the CO 2 RR. Remarkably, Cu@Salen-PIL@Ni(NO 3 ) 2 provides a C2+ faradaic efficiency (FE C2+ ) of 80.9% with partial current density ( j C 2+ ) of 262.9 mA cm −2 at −0.80 V (versus reversible hydrogen electrode, RHE) in 1 m KOH in a flow cell, while Cu@Salen-PIL(Ni) delivers the optimal FE C2+ of 63.8% at j C2+ of 146.7 mA cm −2 at −0.78 V. Mechanistic studies indicates that the presence of Cu–Ni interfaces in Cu@Salen-PIL@Ni(NO 3 ) 2 accounts for the preserve of high-valence Cu(I) species under CO 2 RR conditions. It results in a high activity of both CO 2 -to-CO conversion and C–C coupling while inhibition of the competitive HER.
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PubMed
高影响因子
IONICS
·
2025
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IF 2.6
Wang Zhaomin,Zhao Chaoyue,Niu Xiaodong,Cheng Yong,Wang Limin,Huang Pai
With high theoretical discharge specific capacity, excellent reversibility of electrochemical reaction, and suitable oxygen evolution overpotential, α -Ni(OH) 2 is an auspicious cathode material for alkaline batteries, which supports the development of high-capacity nickel-based batteries. Nevertheless, α -Ni(OH) 2 exhibits substandard structural stability and is susceptible to crystalline transformation, leading to capacity degradation, affecting the battery charge/discharge performance and cycle life. In this study, the TiO 2 -nickel hydroxide (TiO 2 - α -Ni(OH) 2 ) is prepared by high-energy ball milling. Among them, TiO 2 can be uniformly dispersed on the surface of α -Ni(OH) 2 , which can effectively prevent the collapse of the α -phase structure. Benefiting from the unique elemental doping technology, the TiO 2 - α -Ni(OH) 2 composites as a nickel-metal hydride (Ni-MH) battery cathode can release a reversible specific capacity of 390 mAh g −1 at a 2 C rate for 200 cycles. A reversible specific capacity of 210 mAh g −1 is still released after 200 cycles at a 5 C rate. Consequently, TiO 2 - α -Ni(OH) 2 is a promising candidate for high-power Ni-MH batteries.
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JOURNAL OF SOLID STATE ELECTROCHEMISTRY
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2025
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IF 2.6
Bi Mengqi,Liu Wei,Yang Menghui,Huang Naibao
To enhance the corrosion resistance of 316L stainless steel, which is a potential alternative bipolar plate material for PEMWE or PEMFC, Ni–P amorphous coating was prepared by DC electrodeposition method. The results indicated that the coating’s structure strongly related to the phosphorus (P) content. Under specific phosphorus content conditions, a dense coating (Ni–P-30) with typical amorphous characteristics can be obtained, with a uniform surface morphology and no obvious structural defects. In simulated PEMWE environment, Ni–P-30’s corrosion current density decreased by one order of magnitude and the corrosion potential shifted positively by 0.29 V comparing with untreated steel. The excellent corrosion resistance of the amorphous Ni–P coating is attributed by its continuous and dense microstructure, functioning as an effective physical barrier. Meanwhile, during corrosion process, the P will enrich on the surface from the preferential dissolution of nickel in amorphous Ni–P coatings, improving the corrosion potential, reducing the corrosion current and inhibiting the hydration of Ni. Preliminary studies have shown that Ni–P-coated 316L stainless steel can be used as a replacement for graphite as a bipolar plate for PEMWE and PEMFC.
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Advanced Composites and Hybrid Materials
·
2025
·Vol. 8
·期 6
·394
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IF 21.8
Wu Chongji,Yang Lu,Qian Zhu,Yan Zupeng,Sun Xia,Hu Weiqiang,Ma Zongqing
The conventional sintered W-Ni-Fe alloy encounters challenges in achieving both high strength and plasticity simultaneously, primarily due to its inadequate organizational compatibility. To address this issue, we developed a novel approach combining in situ freeze-drying and straightforward liquid-phase sintering techniques to effectively control the microstructure of 93W-4.9Ni-2.1Fe alloys. The corresponding W-Ni-Fe alloy in this work simultaneously takes into account ultrafine W grains (28.3 µm), low W-W connectivity (CW-W = 0.31), and suitable γ phase volume fraction (20.2%), which is currently difficult for traditional W-Ni-Fe alloys to achieve. The minute dimensions of nanopowder play a crucial role in inhibiting Ostwald ripening and facilitating W grain refinement. Additionally, the extensive surface area of nanopowder enhances capillary penetration, leading to effective homogenization of high γ phase volume. As a result, the freeze-dried W-Ni-Fe alloy simultaneously achieves high strength (1010 MPa) and high plasticity (31%), which provides a new insight for the further development of W-Ni-Fe alloy industries.
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Energy Storage Materials
·
2022
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IF 20.831
Tao Zhu,Guoqing Liu,Dongli Chen,Jinxuan Chen,Peng Qi,Jun Sun,Xiaoyu Gu,Sheng Zhang
Parasitic multiscale free radical reactions of electrolytes not only deteriorate battery performance but also cause a fire hazard. Therefore, fundamentally blocking free radical reactions is a smart strategy for simultaneous improvement. Herein, a multiscale free radical annihilating agent hexachlorocyclotriphosphazene cross-linked tannic acid microsphere (HT) is unprecedentedly applied to polyethylene glycol diacrylate based in-situ constructed polymer electrolytes (PEGGPE@HT), which significantly annihilates free radicals from electrolytes at high-voltage and high temperature. The electrochemical stability of PEGGPE@HT is improved to 4.5 V (Li/Li + ). The capacity retention rate of the LiNi 0.8 Mn 0.1 Co 0.1 O 2 (NCM811)//Li cell is increased to 85.3% after 200 cycles at 1 C and that of the LiFePO 4 //Li cell is up to 96.4% after 400 cycles at 1 C by the presence of HT. Moreover, the effectiveness of this strategy has also been further validated in the NCM811//Graphite pouch full cell and high loading NCM811//ultra-thin Li cell. Furthermore, benefiting from the annihilation of phosphorus radicals generated from HT at high temperatures, the PEGGPE@HT shows good flame retardancy and endows the pouch cell with excellent fire safety. Additionally, the pouch cell also features excellent mechanical abuse resistance. This facile synthesis is compatible with the existing battery industry process, which renders great potential for PEGGPE@HT to construct competitive LIBs with high energy density and high safety in large-scale applications.
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Science Bulletin
·
2022
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IF 20.577
Fangyuan Cheng,Xiaoyu Zhang,Peng Wei,Shixiong Sun,Yue Xu,Qing Li,Chun Fang,Jiantao Han,Yunhui Huang
The LiNi 0.8 Co 0.1 Mn 0.1 O 2 (Ni-rich NCM) cathode materials suffer from electrochemical performance degradation upon cycling due to detrimental cathode interface reactions and irreversible surface phase transition when operating at a high voltage (≥4.5 V). Herein, a traditional carbonate electrolyte with lithium difluoro(oxalato)borate (LiDFOB) and tris(trimethylsilyl)phosphate (TMSP) as dual additives that can preferentially oxidize and decompose to form a stable F, B and Si-rich cathode-electrolyte interphase (CEI) that effectively inhibits continual electrolyte decomposition, transition metal dissolves, surface phase transition and gas generation. In addition, TMSP also removes trace H 2 O/HF in the electrolyte to increase the electrolyte stability. Owing to the synergistic effect of LiDFOB and TMSP, the Li/LiNi 0.8 Co 0.1 Mn 0.1 O 2 half cells exhibit the capacity retention 76.3% after 500 cycles at a super high voltage of 4.7 V, the graphite/LiNi 0.8 Co 0.1 Mn 0.1 O 2 full cells exhibit high capacity retention of 82.8% after 500 cycles at 4.5 V, and Li/LiNi 0.8 Co 0.1 Mn 0.1 O 2 pouch cells exhibit high capacity retention 94% after 200 cycles at 4.5 V. This work is expected to provide an effective electrolyte optimizing strategy compatible with high energy density lithium-ion battery manufacturing systems.
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Energy Storage Materials
·
2025
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IF 20.2
Ridong Hu,Chong Mao,Hao Zhuo,Xiaobing Dai,Lewen Yang,Xugang Shu,Yang Li,Zhanqiang Li,Wenhong Ruan,Fujie Yang,Xudong Chen
The precarious interfacial chemistry between the electrode and electrolyte is the determining step that restricts the long cycle life of Ni-rich-based Li-metal batteries. Here we show that the robust cathode electrolyte interphase (CEI) and solid electrolyte interphase (SEI) layers can be engineered by tuning the spatial linking structure of dipentacyclic anhydride (DPA) additives. Specifically, an inorganic-rich CEI/SEI layer induced by CBDA (a DPA featuring a quaternary ring spatial linking structure) exhibits superior Li + interfacial kinetics and an ultra-stable cycle performance, outperforming the other systems. As a result, the NCM811ǁLi cells containing CBDA show excellent long-term performances, even under high voltage, high load, and high charge-discharge current density, respectively. The coin-cell using a low-loading cathode exhibits 129 mAh g- 1 discharged capacity for over 200 cycles at a 6 C rate. Moreover, The high-loading cathode retains 80 % capacity after 312 cycles at 1.0 C. Furthermore, the NCM811ǁLi pouch cell demonstrated a capacity retention rate of 99.8 % after 50 cycles. Prolonged stable cycling for 900 cycles (93 % capacity retention) in an NCM811ǁGraphite pouch cell is enabled by CBDA. The DPA-based additives in this work offer a highly promising and feasible route to achieving a long-term and high-capacity lithium battery featuring a Ni-rich cathode.
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