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JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY · 2019 ·Vol. 19 ·期 7 ·3879-3886 · IF 1.093

Preparation of a Pt/Active Carbon Fiber Catalyst and Its Application in the Synthesis of p-Chloroaniline with Catalytic Hydrogenation

Liu Baoliang,Yang Bing,Sun Meiyu,Qian Xiangli,Zhang Qikun

In this study, a Pt loaded active carbon fiber (Pt/ACF) catalyst was prepared by immobilizing Pt nanoparticles on ACF. The catalyst accelerated hydrogenation of p-chloronitrobenzene (p-CNB) to p-chloroaniline (p-CA) at lower temperature and atmospheric pressure, resulting in approximately 100% yield and selectivity. Several factors that affect p-CA yield were investigated. The nitro reduction rate reached 100% under the optimal reaction conditions, indicating excellent selectivity of the prepared catalyst. This process will overcome the environmental pollution problems associated with the traditional process, and is a green synthetic process.

研究领域: 化学工程 · 环境科学
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Materials Research Express · 2021 ·Vol. 8 ·期 10 ·105009 · IF 1.62

Synthesis of Ag/GO nanocomposite with promising photocatalytic ability for reduction reaction of p-nitrophenol

Pham Tan Thi,Le Van Thang,Tran Van Khai,Tran Xuan Diem,Chau Ngoc Trong Nghia,Tran Thi Thanh Ngan,Le Minh Tri,Nguyen Ngoc Vinh,Nguyen Minh Hien

p-Aminophenol (PAP) is an important intermediate reagent in the synthesis of paracetamol, widely used as an analgesic and antipyretic drug. Therefore, finding an effective catalyst to improve PAP synthesis efficiency is worth studying. Among those studies, nanocomposite is the most promising material. In this study, Ag/GO nanocomposites were synthesized by reducing silver nitrate on graphene oxide (GO) with sodium borohydride as a reducing agent and characterized by SEM, EDX, XRD and UV–vis methods. The catalytic ability was investigated based on the hydrogenation reaction of p-nitrophenol (PNP). We successfully synthesized Ag/GO nanocomposite with relatively homogeneous distributions and similar particle sizes. The results showed that Ag/GO nanocomposite has an excellent catalytic activity with the yield of reduction reaction at 97%, 3 min. Moreover, this photocatalyst can easily be recovered and reused three times without any reaction efficiency reduction. We also successfully synthesized and crystallized PAP with high purity and the total yield of 45.82%. The results show that Ag/GO nanocomposite is an excellent catalyst for high-performance reactions with many useful properties, such as easily recovered and repetitive used. On top of that, Ag/GO nanocomposite is safe, less toxic and environmentally friendly.

CAS / MDL: 16940-66-2
研究领域: 材料科学 · 催化化学 · 环境科学
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Small · 2024 ·Vol. 20 ·期 32 ·2400327 · IF 13

P-Bridging Asymmetry Diatomic Catalysts Sites Drive Efficient Bifunctional Oxygen Electrocatalysis for Zinc-Air Batteries

Nan Wang,Riguo Mei,Liqiong Chen,Tao Yang,Zhongwei Chen,Xidong Lin,Qingxia Liu

Rechargeable zinc-air batteries (ZABs) rely on the development of high-performance bifunctional oxygen electrocatalysts to facilitate efficient oxygen reduction/evolution reactions (ORR/OER). Single-atom catalysts (SACs), characterized by their precisely defined active sites, have great potential for applications in ZABs. However, the design and architecture of atomic site electrocatalysts with both high activity and durability present significant challenges, owing to their spatial confinement and electronic states. In this study, a strategy is proposed to fabricate structurally uniform dual single-atom electrocatalyst (denoted as P-FeCo/NC) consisting of P-bridging Fe and Co bimetal atom (i.e., Fe-P-Co) decorated on N, P-co-doped carbon framework as an efficient and durable bifunctional electrocatalyst for ZABs. Experimental investigations and theoretical calculations reveal that the Fe-P-Co bridge-coupling structure enables a facile adsorption/desorption of oxygen intermediates and low activation barrier. The resultant P-FeCo/NC exhibits ultralow overpotential of 340 mV at 10 mA cm −2 for OER and high half-wave potential of 0.95 V for ORR. In addition, the application of P-FeCo/NC in rechargeable ZABs demonstrates enhanced performance with maximum power density of 115 mW cm −2 and long cyclic stability, which surpass Pt/C and RuO 2 catalysts. This study provides valuable insights into the design and mechanism of atomically dispersed catalysts for energy conversion applications.

研究领域: 材料科学 · 电化学 · 能源转换
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Applied Catalysis O: Open · 2024 · IF 0

P-N bonds in P-modified biochar/g-C3N4 composite constructed via mechanochemical method to enhance photodegradation of indigo carmine

Yongsi Jiao,Cunjun Li,Yanqi Xu,Limei He,Linjiang Wang

Photodegradation of indigo carmine (IC) in wastewater has received much attention in recent decades. However, the current photocatalysts used for IC photodegradation suffer from an unsatisfactory efficiency due to low yield of reactive species. Herein, a P-modified biochar/g-C 3 N 4 (P-BC/CN) photocatalyst was fabricated by mechanochemical method using P-modified biochar and g-C 3 N 4 as precursors. It is discovered that P N bonds were constructed between P-modified biochar and g-C 3 N 4 , and these bonds served as the active sites to promote the generation of •O 2 − during the photodegradation process. The biochar component in P-BC/CN composite is conducive to transfer the photogenerated carriers, thereby avoiding their recombination. The photodegradation experiment showed that the P-BC/CN composite exhibits an impressive photodegradation performance towards IC ( C 0  = 50 mg/L) with a photodegradation rate of 95.3% in 120 min. This work provides a green and efficient method to design biochar-based photocatalyst with P N active sites for advanced wastewater purification.

研究领域: 环境科学 · 材料科学 · 化学工程
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Journal of Materials Chemistry A · 2021 ·Vol. 9 ·期 14 ·9157-9164 · IF 12.732

Development of a bi-compound heterogeneous cocatalyst modified p-Si photocathode for boosting the photoelectrochemical water splitting performance

Zhiwei Chen,Yang Li,Lin Wang,Yuyu Bu,Jin-Ping Ao

In this paper, a MoS2/Rh–P bi-compound heterogeneous cocatalyst is developed to improve the photoelectrochemical (PEC) water splitting performance of a p-Si photocathode. Compared with the single cocatalysts (MoS2 and Rh–P), the bi-compound heterogeneous cocatalyst MoS2/Rh–P on the p-Si photocathode surface exhibits a much better hydrogen evolution reaction (HER) activity at the electrode/electrolyte interface, which is attributed to the synergistic electronic effect between MoS2 and Rh–P materials. Meanwhile, the TiO2 layer could serve as a linker between p-Si and the surface cocatalyst to optimize the interface energy, further promoting the photocarrier transfer process within the system. Thus, the as-prepared p-Si–TiO2–MoS2/Rh–P photocathode exhibits excellent PEC performance with a high photocurrent density of −24.1 mA cm−2 at 0 V (vs. RHE) and a positive onset potential of 0.43 V (vs. RHE). And the bi-compound heterogeneous cocatalyst provides a feasible strategy for boosting the PEC hydrogen evolution.

研究领域: 材料科学 · 能源转换与存储
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MATERIALS SCIENCE FORUM · 2020 · IF 0

Preparation of Thermosensitive Conducting PANI@P(St-NIPAm) Composite Particles and Conductivity Properties

Qiang Zhang,Meng Hao Li,Ru Xiu Wang,Jia Jia Song,Bin Wang,Xin Li,Xiu Juan Fan,Ji Guang Liu

Thermosensitive conducting composite particles were synthesized using the unsulfonated P(St-NIPAm) as a thermosensitive substrate. A series of characterizations have been performed to study the effects of thermosensitive PANI@poly (St-NIPAm) conductivity performance. Aniline diffused into P(St-NIPAm) particles in solution, and then polyaniline (PANI) was in-situ produced in P(St-NIPAm) particles through oxidation polymerization. The samples showed different particle sizes at different temperatures. The content of conducting polyaniline is dependent on NIPAm feed ratios. The particle electrical conductivity was improved with the increasing NIPAM feed ratios and exhibited thermal responsive electrical conductivity. The thermosensitive conducting composite particles will have wide applications in sensors, for example, they could be used to fabricate smart conductive gel responsive to temperature and moisture.

研究领域: 材料科学 · 化学 · 纳米技术 · 电气工程 · 传感器技术
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WATER RESEARCH · 2014 · IF 5.323

Enhanced removal of p-fluoronitrobenzene using bioelectrochemical system

Huajun Feng,Xueqin Zhang,Yuxiang Liang,Meizhen Wang,Dongsheng Shen,Yangcheng Ding,Baocheng Huang,Jiali Shentu

p -Fluoronitrobenzene ( p -FNB) tends to accumulate in industrial effluents because of its recalcitrant properties. Approaches to the removal of p -FNB always encounter conflicts between treatment efficiency and economic efficiency. A bioelectrochemical system (BES) was established to facilitate the removal and mineralization of p -FNB. The treatment cost was reduced by using inexpensive electrode materials and reducing the electrical energy used. p -FNB was effectively removed using the BES, and the reaction rate was higher than the sum of the rates of two control systems, i.e., a biological system (BS) and an electrocatalytic system (ECS), by a maximum of 62.9% under a voltage of 1.4 V. The voltage is a crucial kinetic factor for the BES performance; as the voltage increased from 0 to 1.4 V, the reaction rate constants for p -FNB removal and defluorination increased from 0.0520 to 0.1811 h −1 and 0 to 0.0107 h −1 . The synergistic effect of multistrains gave a TOC removal efficiency in the BES of about 34.05%, yet the removal efficiencies were low for the two control. The defluorination reaction rate was significantly slower than the p -FNB removal rate, which indicated that defluorination lagged p -FNB removal, and p -FNB transformation to p -fluoroaniline ( p -FA) was the fastest step. The electrochemical assistance provided electrons and accelerated the electron transfer rate in the microbial reduction of p -FNB to p -FA. In this study, the critical voltage for defluorination in the BES was 0.8 V, which was approximately 0.2 V lower than that in the ECS. The decrease in the critical voltage for defluorination was based on the production of p -FA, which is more electrocatalytically activated. These results demonstrate the mechanism of efficient p -FNB removal and mineralization in a BES.

CAS / MDL: 140-75-0
研究领域: 环境科学 · 微生物学
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Nanomaterials · 2022 ·Vol. 12 ·期 10 ·1695 · IF 5.719

Constructing Co3O4/La2Ti2O7 p-n Heterojunction for the Enhancement of Photocatalytic Hydrogen Evolution

Haodong Wen,Wenning Zhao,Xiuxun Han

Layered perovskite-type semiconductor La2Ti2O7has attracted lots of attention in photocatalytic hydrogen evolution, due to the suitable energy band position for water splitting, high specific surface area, and excellent physicochemical stability. However, the narrow light absorption range and the low separation efficiency of photogenerated carriers limit its photocatalytic activity. Herein, plate-like La2Ti2O7with uniform crystal morphology was synthesized in molten NaCl salt. A p-n heterojunction was then constructed through the in situ hydrothermal growth of p-type Co3O4nanoparticles on the surface of n-type plate-like La2Ti2O7. The effects of Co3O4loading on photocatalytic hydrogen evolution performance were investigated in detail. The results demonstrate that composite Co3O4/La2Ti2O7possesses much better photocatalytic activity than the pure component. The composite photocatalyst with 1 wt% Co3O4exhibits the highest hydrogen evolution rate of 79.73 μmol·g−1·h−1and a good cycling stability. The photoelectrochemistry characterizations illustrate that the improvement of photocatalytic activity is mainly attributed to both the enhanced light absorption from the Co3O4ornament and the rapid separation of photogenerated electron-hole pairs driven by the built-in electric field close to the p-n heterojunction. The results may provide further insights into the design of high-efficiency La2Ti2O7-based heterojunctions for photocatalytic hydrogen evolution.Keywords:photocatalysis;hydrogen evolution;p-n heterojunction;La2Ti2O7;Co3O4

CAS / MDL: 7647-14-5 10026-22-9
研究领域: 材料科学 · 光催化 · 能源材料
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iScience · 2023 ·Vol. 26 ·期 4 ·106461-106461 · IF 5.8

Multilevel resistive switching in stable all-inorganic n-i-p double perovskite memristor.

Shuaibo Zhai,Jiaqi Gong,Yifei Feng,Zhongbao Que,Weiwei Mao,Xuemin He,Yannan Xie,Xing’ao Li,Liang Chu

Memristors are promising information storage devices for commercial applications because of their long endurance and low power consumption. Particularly, perovskite memristors have revealed excellent resistive switching (RS) properties owing to the fast ion migration and solution fabrication process. Here, an n-i-p type double perovskite memristor with "ITO/SnO 2 /Cs 2 AgBiBr 6 /NiO x /Ag" architecture was developed and demonstrated to reveal three resistance states because of the p-n junction electric field coupled with ion migration. The devices exhibited reliable filamentary with an on/off ratio exceeding 50. The RS characteristics remained unchanged after 1000 s read and 300 switching cycles. The synaptic functions were examined through long-term depression and potentiation measurements. Significantly, the device still worked after one year to reveal long-term stability because of the all-inorganic layers. This work indicates a novel idea for designing a multistate memristor by utilizing the p-n junction unidirectional conductivity during the forward and reverse scanning.

研究领域: 材料科学 · 电子工程 · 纳米技术
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ACS Applied Nano Materials · 2025 · IF 5.5

TiO2-Coated BiOCl Nanosheet p-n Heterojunctions for Photocatalytic H2O2 Production under Simulated Sunlight

Mingming Du,Anxian Peng,Hongyue Liu,Huimei Chen,Qiyun Li,Zheng Fang,Ganning Zeng,Rongjun Yan

The well-designed internal electric field (IEF) with band bending effects will effectively accelerate the separation and transfer of photogenerated charges to foster a photocatalytic performance. Hence, in this work, the IEF-induced BiOCl/TiO2 p-n heterojunctions are prepared through the hydrothermal method for photocatalytic H2O2 production. The BiOCl/2TiO2 composite performed a superior H2O2 yield of 4.75 mM h–1, which is 4 times higher than that of pristine BiOCl. The p-n heterojunction mechanism was investigated via XPS and photoelectrochemical property tests, in which BiOCl/2TiO2 showed the highest photogenerated charge separation efficiency for boosting photocatalytic activity. This work provided an effective strategy for the design of p-n heterojunction photocatalysts to enhance photocatalytic performance.

研究领域: 材料科学 · 环境科学
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MENDELEEV COMMUNICATIONS · 2019 · IF 2.01

UVC-induced photodegradation of p-arsanilic acid assisted by humic substances

Yuliya E. Tyutereva,Peter S. Sherin,Zizheng Liu,Victor F. Plyusnin,Ivan P. Pozdnyakov

Quantum yields of indirect UVC photodegradation of p -arsanilic acid (a widely used phenylarsonic feed additive) caused by the photolysis of humic substances were measured. The acquired results demonstrate that the efficiency of such decomposition of p -arsanilic acid is comparable with that of its direct UVC photolysis due to the participation of active intermediates generated during the photolysis of humic substances. These results could be important for understanding the fate of p -arsanilic acid during an UVC disinfection of wastewaters containing natural humic substances.

CAS / MDL: 65-49-6 1415-93-6
研究领域: 环境科学 · 化学
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CHEMOSPHERE · 2018 · IF 4.427

Phototransformation of p-arsanilic acid in aqueous media containing nitrogen species

Jing Xu,Heng Zhang,Tao Luo,Zizheng Liu,Jun Xia,Xiang Zhang

The effects of co-existing nitrogen species in surface water on the phototransformation of organoarsenical p -arsanilic acid ( p -ASA) have been investigated using a xenon lamp as a simulated solar light source. Significant enhancements of p -ASA phototransformation efficiency were observed in the presence of nitrate and nitrite, increasing with the concentration of these species and pH, whereas ammonia showed no obvious effect. The products, including inorganic arsenic species and organic derivatives, have been analyzed in order to reveal the phototransformation pathways. In the nitrate and nitrite systems, only small proportions of inorganic arsenic species were generated, with the majority of p -ASA being converted into other organoarsenical derivatives through hydroxylation, nitration, and nitrosation. Phototransformation of p -ASA in collected natural surface water was also observed. This work has implications for the phototransformation of p -ASA in nitrogen-contaminated surface water.

CAS / MDL: 65-49-6
研究领域: 环境科学 · 水污染控制 · 光化学反应
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