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NixP
ACS Applied Energy Materials · 2023 · IF 6.4

Cu-Doped ZnIn2S4/NixP Composites with Enhanced Carrier Dynamics and Photocatalytic Hydrogen Production Performance

Tongyang Zhang,Aihua Yan,Sen Luo,Fei Huang,Jixu Zhang,Ye Gao,Wenxue Zhao,Ziwu Liu,Xianhui Zhao

Photocatalytic technology still faces enormous challenges to design and synthesize highly efficient photocatalytic materials with a high electron/hole separation efficiency, rapid charge migration, low carrier recombination rate, and strong visible light-harvesting capability. Herein, Cu-doped ZnIn2S4/NixP (marked CuyZIS/NP) composites were successfully synthesized by a simple two-step method. The synergistic effect of Cu2+ doping and the NixP cocatalyst on hydrogen evolution performance was investigated in detail. The results showed that superior photoactivity over CuyZIS/NP composites was achieved. The optimal Cu0.5ZIS/NP-1/2 sample had a hydrogen evolution rate of 4746.3 μmol·g–1·h–1 under visible light irradiation, which was approximately 15.98 times higher than that of pure ZnIn2S4 (297 μmol·g–1·h–1). This work may offer a valuable insight into understanding the synergistic effect of doping and cocatalysis and provide a guideline for designing and developing highly efficient visible light-driven photocatalysts toward a water splitting system.

研究领域: 材料科学 · 能源化学 · 环境科学
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NEW JOURNAL OF CHEMISTRY · 2022 ·Vol. 46 ·期 13 ·6267-6273 · IF 3.925

NixP and Mn3O4 dual co-catalysts separately deposited on a g-C3N4/red phosphorus hybrid photocatalyst for an efficient hydrogen evolution

Qinyi Mao,Dandan Li,Yuming Dong

Recently, much attention has been focused on the development of photocatalysts for hydrogen evolution. Up to now, efficient hydrogen generation is still greatly challenging due to the restraints of the surface redox reaction rate, and the introduction of a co-catalyst is one of the keys to this problem. Here, dual non-noble co-catalysts NixP and Mn3O4 were proposed and prepared on a g-C3N4/red phosphorus (CNP) hybrid structure with a high light adsorption capability by a two-step photo-deposition method. The photo-excited charge on the composite catalyst separate and transfer from C3N4 to red phosphorous due to a type I heterojunction structure. NixP and Mn3O4 act as reductive and oxidative co-catalysts, respectively. The hydrogen production rate was 5851.3 μmol g−1 h−1, 12.4 times that of pure CNP. The consistent catalytic activity in an actual 25 mL flask for hydrogen evolution over eight hours accumulated 245.08 μmol H2 under solar simulated irradiation. This work provides practical reference for the development of a novel inexpensive photocatalyst system.

CAS / MDL: 7723-14-0
研究领域: 材料科学 · 催化化学
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ACS Applied Energy Materials · 2023 · IF 6.4

Photocatalytic Overall Water Splitting Reaction Feature on Photodeposited NixP/γ-Ga2O3 Nanosheets

Jinni Shen,Xu Liu,Yuhua Zhong,Chengwei Qiu,Huihui Xu,Hongsheng He,Haifeng Li,Jianhan Lin,Zizhong Zhang,Xuxu Wang

Solar light-driven overall water splitting for hydrogen production is an ideal solution to climate warming and energy shortage issues. Obtaining a highly efficient and stable photocatalyst remains a major challenge at present. Herein, NixP/γ-Ga2O3 nanosheets, which were synthesized from NiCl2, NaH2PO2, and home-made γ-Ga2O3 nanosheets by the photodeposition method under 254 UV irradiation for 30 min, are found as a highly active and durable photocatalyst for pure water splitting into H2 and O2 without a sacrificial reagent. The H2 production rate is as high as 5.5 mmol·g–1·h–1 under 125 W high-pressure mercury lamp irradiation, which is 3.4 and 2.5 times higher than that on the pristine γ-Ga2O3 nanosheets and Pt/γ-Ga2O3 nanosheets, respectively, and is 2.0 times higher than that on the 0.5 wt % Ni2P/γ-Ga2O3 reported previously. However, the O2 evolution rate is much less than the H2 evolution rate in the initial reaction stage. On prolonging the irradiation time, H2 evolution declines, while O2 evolution increases until it reaches its stoichiometric value corresponding to H2. The reason for the photocatalytic behavior of NixP/γ-Ga2O3 is studied and the corresponding mechanism is suggested. The absent or low oxygen evolution in the initial reaction stage is because the dioxygen generated from water oxidation by the photogenerated holes is wholly or partially captured by the surface oxygen vacancies to form the surface peroxide bonds (−O–O−). Once the oxygen vacancies are eliminated by the photogenerated O2, the overall water splitting reaction would reach the steady state. Thereafter, H2 production decreases from 5.5 to 2.0 mmol·g–1·h–1, but the O2 evolution gradually approaches the corresponding stoichiometric value, especially for the photocatalyst treated with H2O2 for 24 h.

CAS / MDL: 69365-72-6
研究领域: 材料科学 · 催化 · 可再生能源 · 光化学
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Catalysis Science & Technology · 2025 · IF 4.2

Construction of a 0D/2D NixP/LaTiO2N Schottky junction photocatalyst for efficient visible-light-driven photocatalytic CO2 reduction

Guoyu Xu,Yanan Chen,Peiling Lin,Zizhong Zhang,Tao Ji,Wenyue Su

Employing photocatalytic technology to transform CO2 into valuable fuels is considered a promising solution for addressing the exacerbated greenhouse effect and energy crisis. The development of photocatalysts featuring superior charge separation efficiency is pivotal for the widespread implementation of photocatalytic CO2 reduction technologies. Herein, zero-dimensional (0D) NixP nanoparticles are anchored onto two-dimensional (2D) LaTiO2N nanosheets by a photo-deposition method, and a NixP/LaTiO2N Schottky junction composite with excellent photocatalytic CO2 reduction performance is constructed. The optimal NixP/LaTiO2N composite achieves CO and CH4 yields of 9.39 and 4.15 μmol g−1 h−1, respectively, with the utilized photoelectron number (UPN) reaching 51.98 μmol g−1, which is approximately 9.7 times higher than that of LaTiO2N alone. The improved photocatalytic performance of the composites can be attributed to the formation of Schottky junctions, which effectively suppress the recombination of photogenerated carriers. This study provides a new idea for the development of 0D/2D Schottky junction photocatalysts.

CAS / MDL: 10277-43-7
研究领域: 材料科学 · 环境科学 · 能源科学
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Journal of Environmental Chemical Engineering · 2022 · IF 7.968

Photocatalytic removal of sulfamethoxazole using yeast biomass-derived NixP/biocarbon composites in the presence of dye sensitizer

Xuqian Wang,Yuanyuan Peng,Tonghui Xie,Yongkui Zhang,Yabo Wang,Huan Yang

Photocatalysis represents an environmental-benign approach for organic pollutant treatment. Herein, a photocatalytic system composed of Ni x P/biocarbon composite as reactive center and erythrosine B (ErB) as sensitizer was constructed for the removal of sulfamethoxazole (SMX) antibiotic under visible light irradiation. Ni x P/biocarbon composites were fabricated via a facile impregnation-pyrolysis approach using baker’s yeast as both phosphorus and carbon precursor. It was found that Ni x P with pure Ni 12 P 5 , almost pure Ni 2 P or mixed crystal phases could be obtained by simply adjusting Ni:P molar ratio in precursor and pyrolysis temperature. Interestingly, the variation of Ni x P crystal phases remarkably affected photocatalytic removal efficiency of SMX. The obtained Ni x P(1:4)− 900 sample with mixed phases of Ni 12 P 5 and Ni 2 P displayed excellent photodegradation performance with 98.71% removal efficiency for SMX ( C 0 = 20 mg L −1 ) in ErB-sensitized photocatalytic system. Moreover, the reusability of Ni x P/biocarbon composite was confirmed by four consecutive runs. The slight loss of activity in recycle study could be fully recovered after thermal regeneration. Further investigation indicated that photo-generated electrons from excited ErB molecules could be transferred to Ni x P/biocarbon, triggering a series of reactions to form various reactive oxygen species (eg., •O 2 − , H 2 O 2 , •OH) for SMX degradation. The better photocatalytic activity of Ni x P mixed crystal phases should be ascribed to its faster electron transfer ability. Overall, this study provides useful guidance in terms of the development of transition metal phosphide and efficient photocatalytic system.

研究领域: 环境科学 · 材料科学 · 化学工程 · 光化学
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CHEMICAL ENGINEERING JOURNAL · 2018 · IF 6.735

One-step co-electrodeposition of hierarchical radial NixP nanospheres on Ni foam as highly active flexible electrodes for hydrogen evolution reaction and supercapacitor

Xueying Cao,Dedong Jia,Da Li,Liang Cui,Jingquan Liu

Considering the synergistic effect of transition metal phosphides and 3D structure substrates, herein, we directly deposited well-defined hierarchical radial Ni x P nanospheres on Ni foam via a facile, one-step co-electrochemical method to function as highly active flexible electrodes for both hydrogen evolution reaction and supercapacitor. Impressively, the bifunctional Ni x P/NF electrode requires an overpotential of only 63 mV to achieve a current density of 10 mA cm −2 and demonstrates a low Tafel slop of 55 mV dec −1 in 1 M KOH. Moreover, the electrochemical supercapacitor based on this hierarchical Ni x P/NF electrode also shows a superior specific capacitance of 1684 mF cm −2 (382.7 F/g) at a current density of 2 mA cm −2 and an outstanding retention ratio of 110.9% of its original capacitance value after 4000 cycles in 6 M KOH. Hopefully, excellent electrochemical performances demonstrate that this Ni x P/NF material could be a promising candidate for future applications in both hydrogen evolution reactions and supercapacitors.

CAS / MDL: 31175-20-9 7440-06-4
研究领域: 材料科学 · 电化学
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