Materials Research Express
·
2021
·Vol. 8
·期 12
·125006
·
IF 1.62
Peng She,Chun Yao,Jun Li,Hegang Bao,Xiuquan Xu,Hong Zhou
Co-doping is one of the most facile and efficient strategies for boosting the photocatalytic performance of g-C3N4. Herein, a series of Ti and O co-doped g-C3N4 (Ti/OCN) composites with excellent photocatalytic inactivation activity of Enterobacter cloacae (E. cloacae) were successfully synthesized by simple calcination of urea/formic acid/TiCl4 precursor. The obtained Ti/OCN-3 possessed the optimal photocatalytic capability with complete inactivation of 6.20 log CFU·ml−1 E. cloacae under 60 min of visible light irradiation. The improved photocatalytic disinfection performance was probably attributed to the synergistic effect of Ti and O co-doping, which led to an extended visible light response and accelerated charge transport efficiency. Furthermore, scavenger trapping and electron spin resonance (ESR) experiments revealed that ·O2−, h+ and ·OH were responsible for the enhanced inactivation activity. Overall, this research provided a promising strategy for fabricating g-C3N4-based catalysts to efficiently deal with the hazards of pathogenic microorganisms.
研究领域:
环境科学
·
微生物学
·
材料科学
✓ 已验证
DOI
高影响因子
DIAMOND AND RELATED MATERIALS
·
2024
·
IF 4.3
Shuai Yang,Tao Li,Jun Fang,Shichong Yao,Zhenyu Li,Yunyun Liu,Jie Chen,Yuanliang Yuan,Xiaocong Zhong
N,O-codoped microporous carbon (HPC) was derived from hypnum plumaeforme via precarbonization and KOH activation and utilized as an electrode for supercapacitors. The HPC750 sample, produced at an activation temperature of 750 °C, demonstrated superior capacitive behavior due to its large specific surface area, microporous architecture, and high number of oxygen and nitrogen heteroatoms. These HPC750 electrodes have a specific capacitance of up to 424 F g −1 at a current density of 1 A g −1 while also providing excellent rate performance, maintaining >85 % capacitance over a range of 1 to 100 A g −1 . In a symmetric supercapacitor configuration using 6 M KOH and 1 M Na 2 SO 4 as electrolytes, the HPC750 electrodes exhibit high specific capacitances of 96.2 F g −1 and 65.8 F g −1 at a current density of 1 A g −1 , respectively. With the Na 2 SO 4 electrolyte, the device achieved a peak energy density of 29.9 W h kg −1 and a peak power density of 225 W kg −1 . In addition, the electrodes retained approximately 90 % of their initial capacitance after 15,000 cycles at a current density of 5 A g −1 .
研究领域:
材料科学
·
能源存储
·
植物学
✓ 已验证
DOI
高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2021
·
IF 5.316
Shiying Lin,Lanlan Mo,Feijun Wang,Ziqiang Shao
Heteroatom doping is a significant modification of carbon materials for electrodes in storage device and co-doping has synergistic improvement effect. This work reports a N/O co-doped porous carbon (CPK800) from crosslinking sodium carboxymethyl cellulose and poly (m-phenylene diamine). The material characterization reveals its large specific surface area of 1501.3 m 2 g −1 with optimum micro- and mesopore distribution, partially graphitized carbon and high N, O concentration. This carbon has 3D interconnected porous structure and internal conducting network providing rapid ion and electron transportation. Take these advantages, it exhibits high capacitance of 358 F/g at 1 A g −1 , an excellent rate retention of 70.8% at a high current density of 20 A g −1 , and superior cyclic stability of 97.8% capacitance retention after 10,000 cycles at 10 A g −1 as an electrode material in 3 M KOH electrolyte. Moreover, the assembled symmetric supercapacitor device (CPK800//CPK800) delivers a high energy density of 11.5 Wh kg −1 at a power density of 326.8 W kg −1 and still have energy density of 8.9 Wh kg −1 at a very high power density of 6.8 kW kg −1 . The well-developed structure and outstanding electrochemical performance demonstrate the promising potential of CPK800 as electrode material for advanced energy storage devices.
研究领域:
材料科学
·
能源存储
✓ 已验证
DOI
高影响因子
Journal of Environmental Chemical Engineering
·
2024
·
IF 7.4
Min Zhang,Mingxuan Du,Yuhang Ren,Yun Zhu,Yunyuan Dong,Jianming Liao,Xiaobin Chen,Qifu Zheng,Hongfei Yin
Element doping is generally employed to modify photocatalysts by optimizing their electronic structure, and light absorption , as well as improving charge separation and transfer, which are key factors in photocatalysis . In this study, a simple one-step solvothermal route was employed to synthesize N, O co-doped ZnIn 2 S 4 . Systematical analyses demonstrate that the introduction of N and O co-doping leads to enhanced light absorption, increased specific surface areas , and improved charge separation and transfer in comparison to the unmodified ZnIn 2 S 4 . As expected, compared with bare ZnIn 2 S 4 , the as-prepared N, O co-doped ZnIn 2 S 4 exhibits superior photocatalytic H 2 evolution and Cr(VI) photoreduction performance. The H 2 evolution rate of the N, O co-doped ZnIn 2 S 4 reaches 2254.0 μmol g −1 h −1 , which is 2.8 times of pristine ZnIn 2 S 4 . Moreover, the Cr(VI) photoreduction efficiency reaches 99.5 % within 50 minutes, and the apparent kinetic constant is nearly 4 times the bare ZnIn 2 S 4 . This work contributes to the modification of ZnIn 2 S 4 for photocatalytic H 2 generation and Cr(VI) reduction.
研究领域:
材料科学
·
环境科学
·
能源科学
✓ 已验证
产品关联
DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2024
·
IF 13.3
Jialin Li,Yu Wang,Ye Zhang,Wei Zhao,Wenzhe Bao,Yufeifan Duan,Junwei Yu,Bo Zhu,Kun Qiao
Currently, the hydrogen storage application of carbon-based adsorbent materials is mostly implemented under the pressure conditions of 30–300 bar, while there is few targeted studies conducted on the unsaturated adsorption under ambient pressure conditions. Therefore, based on industrialized Lyocell biopolymer fiber precursors and the enhancement effects of dipole-induced hydrogen bonds (DIHB), this work presents a facile construction strategy for P/O co-doped Lyocell-based porous carbon fiber cloth (Ly-ACF-F40). By the technical route of thermal stabilization---sonication assisted phosphoric acid activation---hydrogen bonds introduced by interfacial fluorination, the constructed Ly-ACF-F40 acquires a high specific surface area (1870 m 2 /g) and total pore volume (1.277 cm 3 /g), and an excellent hydrogen storage capacity of 3.22 wt% under ambient pressure conditions (77 K, 1 bar). The study directly demonstrated in the experiment that dipole induced hydrogen bonding H(I)-H(II)···F can effectively enhance the atmospheric hydrogen storage density on the basis of other eliminating influencing factors of specific surface area. The simple construction strategy of porous carbon-based materials can provide reference for the research of unsaturated adsorption hydrogen storage materials under ambient pressure conditions, also assist in the application and promotion of low-cost solid hydrogen storage materials.
研究领域:
材料科学
·
能源存储
✓ 已验证
产品关联
DOI
高影响因子
NEW JOURNAL OF CHEMISTRY
·
2024
·Vol. 48
·期 46
·19508-19518
·
IF 2.7
Yuanyuan Wang,Yingjing Xia,Xingshen Dong,Wenyi Wang,Xueqin Wang,Yanxiu Liu,Peng Qiao,Geng Zhang,Shetian Liu
Supercapacitors, an innovative energy storage technology, combine the strengths of batteries and capacitors, enabling diverse applications in sectors such as communications, transportation, and aerospace. Porous carbon materials derived from biomass have excellent electrical conductivity, customizable dimensions, high surface area, and robust electrochemical stability, rendering them ideal candidates for supercapacitor electrodes. This research utilized edamame shells as the carbon precursor and KOH as the activating agent to synthesize a series of N/O co-doped porous carbons (ESC-x-800) through a combined pre-carbonization and activation process. This study thoroughly investigated the effect of KOH addition on the morphology, structure, and electrochemical performance of the materials. The result showed that the ESC-3-800 stood out as the top performer, distinguished by its unique self-doping characteristic with N and O atoms and a unique hierarchical porous structure. The ESC-3-800 boasted an impressive specific surface area of 3188.98 m2 g−1, coupled with a substantial pore volume of 1.86 cm3 g−1. When evaluated in a three-electrode system, ESC-3-800 demonstrated a remarkable specific capacitance of 301 F g−1, and a capacitance retention rate of 73.1% at a high current density of 20 A g−1. In a two-electrode setup, the ESC-3-800 achieved a notable high energy density of 37.6 W h kg−1 (at a power density of 200 W kg−1) in the 1 M Na2SO4 electrolyte. Remarkably, after enduring 12 000 charge–discharge cycles in 6 M KOH, it maintained an impressive 96.68% of its initial capacity (8 A g−1), demonstrating exceptional long-term stability and durability. The straightforward preparation method and outstanding performance of the edamame shell-derived N/O co-doped porous carbon underscore its immense potential for practical applications in supercapacitors.
研究领域:
材料科学
·
能源存储技术
·
生物质利用
✓ 已验证
产品关联
DOI
高影响因子
APPLIED SURFACE SCIENCE
·
2021
·
IF 6.707
Weili Teng,Qinqin Zhou,Xuekai Wang,Haibing Che,Yucheng Du,Peng Hu,Hongyi Li,Jinshu Wang
Heteroatom-doped hierarchically porous carbon is attractive electrode material for supercapacitors. However, it still remains a great challenge to develop a high-performance supercapacitor electrode with efficient preparation strategy. Herein, we report a N,O-codoped hierarchically porous carbon (NOHPC) prepared through one-step carbonization/in-situ doping/activation process by using natural diatomite as template and polydopamine as precursor. The as-prepared NOHPC possesses synergistic advantages of abundant redox-active N,O dopants, large effective specific surface area and hierarchically porous (micropores, mesopores and macropores) structure. Benefiting from such advantages, the NOHPC electrode exhibits an extremely high specific capacitance of 436.0 F g −1 at 0.625 A g −1 in H 2 SO 4 electrolyte. The as-assembled supercapacitor in H 2 SO 4 electrolyte also yields high specific capacitance (328.3 F g −1 at 0.625 A g −1 ), excellent rate performance (74.8% capacitance retention, 0.625–25 A g −1 ) and superb cycling stability (93.9%, 10,000 cycles). Besides, the corresponding device in Na 2 SO 4 electrolyte can present an enhanced energy density of 23.4 Wh kg −1 at the power density of 358.8 W kg −1 (1 A g −1 ) and still maintain 15.0 Wh kg −1 at the power density of 8357.8 W kg −1 (25 A g −1 ). The outstanding electrochemical performance and the efficient preparation process of NOHPC make it a promising widely applied electrode material for supercapacitor.
研究领域:
材料科学
·
能源存储
·
纳米技术
✓ 已验证
产品关联
DOI
高影响因子
DYES AND PIGMENTS
·
2019
·
IF 4.018
Xiuquan Xu,Songmei Wang,Tongjie Hu,Xiaofeng Yu,Jiapeng Wang,Chao Jia
Co-doping has been proven to significantly enhance the photocatalytic performance of g-C 3 N 4 . Herein, Mn and O co-doped g-C 3 N 4 (Mn/O-CN) composites were constructed for the first time by a simple one-pot calcining route. The systematic characterization results of XRD , FT-IR, TEM-EDS, XPS and DRS revealed that the Mn and O elements were co-doped into the CN framework successfully as Mn 3+ / 4+ and n-π* conjugate forms, respectively. The as-prepared Mn/O-CN-2 achieved the highest visible-light-driven degradation rate constant of 0.0290 and 0.0267 min −1 for degradation of Malachite green (MG) and Amido black 10B (AB 10B), which were about 5.09 and 5.45 folds higher than that of pristine CN, respectively. The improved photocatalytic degradation property of Mn/O-CN were mainly benefited from the extended visible light utilization, the enlarged specific surface area, and the accelerated separation and transfer of photo-induced charge carriers, which were all induced by the synergistic effects of Mn and O co-doped. Finally, the active species capturing experiments proved that the superoxide radicals (·O 2 − ) and holes (h + ) acted as the predominant roles in the photocatalytic degradation process .
研究领域:
材料科学
·
环境科学
✓ 已验证
产品关联
DOI
高影响因子
LANGMUIR
·
2024
·
IF 3.7
Liye Ni,Guangjie Yang,Chenweijia He,Tiancheng Lan,Shuijian He,Haoqi Yang,Nan Wu,Rulan Chen,Li Liu,Fangdi Wu,Qian Zhang
The preparation of porous carbon is constrained by the extensive use and detrimental impact of activators and dopants. Therefore, developing green and efficient strategies that leverage the intrinsic properties and pretreatment of the materials to achieve self-activation and self-doping is particularly crucial for porous carbon materials. Herein, potassium histidine was utilized as the molecular salt precursor, attaining the efficient and streamlined preparation of porous carbon through a one-step carbonization process that enables self-activation, self-doping, and self-templating. More interestingly, the carbonization temperature significantly impacts the porous structure of the molecular salt precursors, the properties of the heteroatoms, and electrochemical performance. The designed electrodes exhibit high accessibility to electrolyte ions and effective ion-electron transport channels. Therefore, the optimal carbon material (KHis800) has an excellent mass-specific capacitance of 305.2 F g–1 at 0.2 A g–1, and a high capacitance retention rate of 115.6% (50,000 cycles at 5 A g–1). Notably, KHis800 also shows a maximum energy density of 19.6 Wh kg–1. This research is dedicated to exploring a more efficient preparation method for porous carbon material via molecular salts, offering insights for the sustainable development of carbon materials.
研究领域:
材料科学
·
电化学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2021
·
IF 13.273
Wen-Long Yu,Shi-Lei Zhao,Guang-Wen Xu,Xin Li,Xiao-Lei Zhang,Yu-Ling Shan,Jun-Wei Ding,Guo-Hui Qin,Jun-Mei Zhang,Xiang Feng,De Chen
The chloroxylenol (PCMX) has shown well virucidal efficacy against COVID-19, but the large-scale utilization of which will undoubtedly pose extra environmental threaten. In the present study, the recycled industrial phenylenediamine residue was used and an integrated strategy of “carbonization-casting-activation” using super low-dose of activator and templates was established to achieve in-situ N/O co-doping and facile synthesis of a kind of hierarchical hyperporous carbons (HHPC). The sample of HHPC-1.25–0.5 obtained with activator and template to residue of 1.25 and 0.5 respectively shows super-high specific surface area of 3602 m 2 /g and volume of 2.81 cm 3 /g and demonstrates remarkable adsorption capacity of 1475 mg/g for PCMX in batch and of 1148 mg/g in dynamic column adsorption test. In addition, the HHPC-1.25–0.5 exhibits excellent reusability and tolerance for PCMX adsorption under various ionic backgrounds and real water matrix conditions. The combined physio-chemistry characterization, kinetic study and DFT calculation reveal that the enhanced high performances originate from the hierarchical pore structure and strong electrostatic interaction between PCMX and surface rich pyridinic-N and carbonyl groups.
研究领域:
环境科学
·
材料科学
✓ 已验证
DOI
高影响因子
NEW JOURNAL OF CHEMISTRY
·
2021
·Vol. 45
·期 36
·16648-16657
·
IF 3.591
Jing-Jiang Liu,Zhi-Wei Yan,Rui-Xue Kang,Jin-Hui Wang,Xun Feng
Herein, unique N,O-codoped porous biocarbon (PB) was prepared using Ephedra Herb (EH) as a precursor via a green and sustainable NaCl-sealing strategy and subsequent pyrolysis method. PB possesses vast microstructure, interlinked pores, and high specific surface area, which can facilitate ion adsorption and buffering to improve its properties as an electrode material. In addition, the high specific surface area, well-developed porosity, and abundant heteroatoms in EH are retained well owing to the salt-sealing approach, contributing to additional pseudocapacitance. Therefore, a typical PB sample (S12), obtained from the NaCl-sealing and pyrolysis of the mixture of EH and NaCl at a mass ratio of 1 : 2, is endowed with high specific capacitance, excellent rate performance, and performance retention over long-term cycling. Most importantly, an aqueous symmetrical supercapacitor (S12//S12) assembled with S12 electrodes has a superior specific energy density of 11.6 W h kg−1 at a specific power density of 450.1 W kg−1 in Li2SO4 electrolyte. This work confirms the utility of a NaCl-sealing strategy for designing high specific surface area biocarbon materials that are ultra-rich in micropores, and it sheds some light on the use of sustainable and low-cost synthetic carbon that is ultra-rich in micropores to meet energy-storage device requirements.
研究领域:
材料科学
·
能源存储
·
环境科学
✓ 已验证
产品关联
DOI
高影响因子
CARBON
·
2021
·
IF 9.594
Mengmeng Yang,Qingquan Kong,Wei Feng,Weitang Yao
In this study, N/O co-doped cage-type biomass carbon (NOBC) was prepared through a simple and facile hydrothermal reaction and two-step carbonization method. As the anode of a potassium ion battery, NOBC displays a superhigh long-cycling performance and a super high rate performance. NOBC-2 provides an excellent reversible capacity of 251.2 mAh g −1 after 1500 cycles at 0.5 A g −1 , and an excellent performance of 334.6 mAh g −1 at a high current density of 5 A g −1 (after 2000 cycles). The reversible capacity of 124.19 mAh g −1 can be maintained even after 5000 cycles at 10 A g −1 . The excellent performance of NOBC is attributed to the unique hollow cage structure, internal 3D carbon network structure and N/O co-doping. Based on the results of detailed fundamental analysis, the pseudo-capacitance mechanism contributes to the higher K ion storage process in NOBC-2. Density functional theory (DFT) calculations further show that N/O double doping can promote the adsorption of K ions in biomass carbon materials and improve the conductivity of the materials. The simple synthesis route and excellent electrochemical performance provide new insights for the search for novel carbon-based K storage anode materials with high energy and long cycle life.
研究领域:
材料科学
·
能源存储
✓ 已验证
产品关联
DOI
高影响因子
危险品化学品经营许可证（带存储）