APPLIED SURFACE SCIENCE
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2021
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IF 6.707
Xiaoxue Zhao,Linlin Sun,Xian Jin,Mengyang Xu,Shikang Yin,Jinze Li,Xin Li,Dong Shen,Yan Yan,Pengwei Huo
Z-scheme heterojunction can effectively separate photo-generated carriers and enhance photocatalytic activity of CO 2 reduction. In this work, we report indirect Z-scheme heterojunction of UiO-66-NH 2 /Cu 2 O/Cu, which achieves highly CO 2 photocatalytic conversion to CO. Among these, UiO-66-NH 2 /Cu 2 O/Cu-0.39 (U/C/Cu-0.39) displays the best activity with a CO yield of 4.54 μmol·g −1 ·h −1 , which is 37.8 times higher than that for UiO-66-NH 2 and 50.4 times higher than that for Cu 2 O. Cu not only acts as the electron conductor of the indirect Z-scheme heterojunction to promote the charge carrier transmission, but also acts as the active site of CO 2 reduction. The increase of active sites and the CO 2 adsorption capacity results in the superior photocatalytic performances.
研究领域:
材料科学
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化学
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环境科学
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产品关联
DOI
高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
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2024
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IF 9.4
Luotian Lv,Yao Liu,Yankai Huang,Tong Li,Han Feng,Yongqing Wang
Since the intensification of global environmental pollution and energy shortages, photocatalytic CO 2 reduction reaction (CO 2 RR) has emerged as a promising strategy to convert solar energy into clean chemical energy. Herein, we construct a robust and efficient heterojunction construction photocatalyst for CO 2 RR, composed of the highly reactive CeNi quantum dots (CeNi QDs) and nickel metal–organic layer (Ni-MOL) ultrathin nanosheets. This design facilitates the rapid separation of photogenerated charge carriers, as confirmed by X-ray photoelectron spectroscopy (XPS), photoluminescence spectroscopy (PL) and other characterizations. Mechanistic studies with in situ diffuse reflectance Fourier transform infrared spectroscopy (in situ DRIFTS) and the d-band center calculation indicate that the propensity of photocatalyst for CO 2 absorption and CO desorption, leading to high performance and selectivity. The optimized loading amount of CeNi quantum dots and modified structure result in a CO yield of 30.53 mmol·g −1 within 6 h under irradiation. This work not only paves a new and convenient way for developing high-activity quantum dot materials for CO 2 RR but also exploits novel avenues to fabricate more heterojunction composites for solar energy conversion.
研究领域:
材料科学
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环境科学
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能源科学
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化学工程
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产品关联
DOI
PubMed
高影响因子
CATALYSIS TODAY
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2022
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IF 6.562
Xiaowen Su,Shan Wu,Xiaoxing Long,Yan Shi,Qi Pan,Jixin Su
Preventing climate change and achieving carbon neutralization depend on strengthening the carbon cycle in industry and limiting carbon emissions to ambient air. Our aim is to reduce CO 2 to valuable CO by gas-solid photo-catalytic reduction under sunlight. We prepared catalysts by one-step synthesis with graphene oxide (GO) and ZnO, surface modified with a monolayer of sulfonated cobalt phthalocyanine (CoPcS), which were calcined to obtain photocatalyst samples containing Co(II), ZnO and reduced graphene oxide (rGO). Results of TEM, SEM-EDS, XRD, XPS, PL and ESR revealed that the photocatalyst samples possessed a hybrid layer microstructure, heterojunction, and excellent electron-hole pair separation. Evaluation of the photocatalytic reduction reactivity showed that CO selectivity reached 96.2–99.0% and top CO yield was 26.15 µmol.g −1 .h −1 .
研究领域:
环境科学
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材料科学
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化学工程
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光化学
✓ 已验证
DOI
高影响因子
FUEL PROCESSING TECHNOLOGY
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2023
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IF 7.5
Yuanling Li,Han Yu,Jing Dai,Zhenzong Zhang,Zhichao Zhang,Hongbing Yu,Lina Liu
Non-thermal plasma (NTP) combined with catalysts supplies a potential alternative to enable the CH 4 and CO 2 conversion to work at low temperatures. In this study, different Ni/BN catalysts were synthesized using modified wetness impregnation for CH 4 and CO 2 conversion in dielectric barrier discharge (DBD) plasma. Among, BN_IPA_Ni exhibited the highest catalytic performance with a CH 4 conversion of 40.5%, a CO 2 conversion of 26.6%, a H 2 yield of 9.3% and a CO yield of 10.5%. The development of B O defects, which played a significant role in the size control of Ni particles to facilitate the dissociation of CH 4 to form H*, is the key for the high catalysis activity and selectivity in this reaction. In addition, the B O defects of BN_IPA_Ni provide an efficient route to eliminate excess CH x species, which further inhibit the nucleation growth of carbon species to inert carbon.
研究领域:
化学工程
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催化
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等离子体化学
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环境科学
✓ 已验证
产品关联
DOI
高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
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2022
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IF 9.136
Longkai Pan,Minggang Zhang,Hui Mei,Li Yao,Zhipeng Jin,Hongxia Liu,Shixiang Zhou,Ziyi Yao,Gangqiang Zhu,Laifei Cheng,Litong Zhang
Use of 3D photocatalytic reactor has been widely explored for development of efficient photocatalytic systems. In the present study, a bionic palisade cells BiOBr/Sr 2 Nb 2 O 7 /Al 6 Si 2 O 13 photocatalytic reactor with high strength was prepared through combination of 3D printing technology and solvothermal method. The carefully designed and optimized bionic palisade cell structure exhibited a periodic porous structure with high surface area. The controllable periodic structure effectively regulated the internal photon transfer and mass transfer. Photon transfer ensured that light is fully scattered within the structure, which improved light utilization. High mass transfer ensured smooth flow of reactant inside the structure, which increased reactant adsorption on the surface of photocatalysts. The interface electric field of the BiOBr/Sr 2 Nb 2 O 7 p-n heterojunction effectively separated the photogenerated electrons and holes. The BOB/SNO/ASO structure had high photocatalytic CO 2 reduction performance under the simulated sunlight. The CO yield for the reaction was 13.68 μmol/g/h, whereas that of CH 4 yield was 6.37 μmol/g/h. Therefore, the findings of the present study provide a basis for design and preparation of high-performance 3D photocatalytic reactors.
研究领域:
材料科学
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环境科学
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化学工程
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光催化
✓ 已验证
DOI
高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
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2024
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IF 8.1
Min Wang,Jing Xie,Zhenjiang Lu,Fanlin Kong,Baolin Liu,Zhende Wu,Yali Cao
The structural devise of photocatalytic materials are closely related to the separation of photogenerated carriers and the transport of charge, which is crucial to enhance the performance of photocatalytic carbon dioxide reduction reaction (CO 2 RR). Here, a photocatalyst (CdS-S V @Co@NCNT) has been successfully prepared by growing cadmium sulfide nanoparticles with sulfur vacancies on N-doped carbon nanotubes through a simple solvothermal method. The intrinsic electronic structure is regulated by sulfur vacancies to promote photocatalytic activity. Meanwhile, a larger specific surface area of Co@NCNT could expose more reaction sites and shorten the transfer distance of photogenerated carriers. Furthermore, the combination with Co@NCNT could effectively suppress the photocorrosion of CdS. The possible photocatalytic CO 2 RR path is further speculated by in-situ infrared test results, in which CO 2 molecules adsorbed on sulfur vacancies preferentially generate important intermediate COOH*, which is then reduced to CO and CH 4 . Therefore, it exhibits a high CO yield of 263.3 μmol·g −1 ·h −1 and trace of CH 4 while showing excellent stability. This research provides a novel idea for designing the photocatalysts with highly active and stability for CO 2 RR.
研究领域:
材料科学
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化学工程
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环境科学
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纳米技术
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产品关联
DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
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2024
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IF 13.3
Qiliang Zhu,Wenxuan Huang,Jianhua Shen,Haibo Jiang,Yihua Zhu,Chunzhong Li
Metal halide perovskite nanocrystals have garnered significant attention in the realm of photocatalytic CO 2 reduction in recent years owing to their remarkable reducing properties and high selectivity. However, the issue of low photocatalytic activity due to severe carrier recombination phenomena in perovskite has posed a significant challenge. To address this, a one-pot in-situ preparation strategy was employed to create a BiOBr/Bi-doped perovskite nanocrystal S-scheme heterojunction, resulting in a significant improvement in the CO 2 photoreduction performance. The heterojunction material exhibited a CO yield of 151.56 μmolg -1 h −1 , with a selectivity for CO of 93.6 %. The molar ratio of the components was modulated using an in-situ water aging strategy, yielding a photocatalyst performance that exceeded that of pure BiOBr. The synthesis strategy of one-step in-situ preparation of heterojunctions overcomes the problem of insufficient bonding caused by two-step methods. And various characterizations and DFT calculations strongly support the S-scheme mechanism of the photocatalyst. The active site effectively reduces the energy barrier for the transition from *COOH to *CO intermediate, thereby significantly improving photocatalytic activity.
研究领域:
材料科学
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光催化
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纳米技术
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环境科学
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化学工程
✓ 已验证
产品关联
DOI
高影响因子
APPLIED CATALYSIS B-ENVIRONMENTAL
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2022
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IF 24.319
Xinxin Han,Bingjie Lu,Xin Huang,Cheng Liu,Shixia Chen,Jingwen Chen,Zheling Zeng,Shuguang Deng,Jun Wang
S-scheme photocatalysts are more efficient than the conventional type-II configuration, but the CO 2 reduction performances are still unsatisfactory. Herein, we firstly report the layered double hydroxide (LDH) based S-scheme heterostructure photocatalyst (NiIn LDH/In 2 S 3 ) with n-type NiIn LDH and p-type In 2 S 3 . The built-in internal electric field directs the photogenerated electrons flow from the conductive band of In 2 S 3 to the valance band of NiIn LDH, which is confirmed by operando and theoretical experiments. The CO 2 photoreduction intermediates are monitored by in-situ Raman spectra, and the density functional calculations disclose the reduced energy barrier for CO desorption on the heterojunction. Therefore, without cocatalysts or sacrificial agents, the NiIn LDH/In 2 S 3 heterojunction delivers a high CO yield rate of 29.43 μmol g −1 h −1 under visible light irradiation, ca. 3.5 and 4.3 times higher than the single counterpart NiIn LDH and In 2 S 3 . Notably, this value is the highest among S-scheme CO 2 photocatalysts and surpasses most top-ranking benchmarks.
研究领域:
材料科学
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化学
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环境科学
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF THE ENERGY INSTITUTE
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2024
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IF 5.6
Zheng Bo,Mengyu Cao,Yaolin Wang,Jianhua Yan,Kefa Cen,Xin Tu
Plasma catalytic CO 2 hydrogenation has emerged as a promising approach for converting CO 2 into valuable chemicals such as CO, offering a potential solution to mitigate greenhouse gas emissions. In this study, we investigate the synergistic effect between plasma and a Cu/Ti 3 C 2 T x MXene catalyst for CO 2 hydrogenation via the reverse water gas shift (RWGS) reaction in a dielectric barrier discharge (DBD) reactor. Our findings reveal a significant enhancement in CO 2 conversion (33.1%) and CO yield (31.9%) when using the Cu/Ti 3 C 2 T x catalyst compared to plasma alone or with a Ti 3 C 2 T x foam. Plasma treatment creates unsaturated Ti sites on the Ti 3 C 2 T x surface, dramatically improving CO 2 adsorption and activation, while Cu nanoparticles significantly enhances the activation and dissociation of H 2 molecules on the catalyst surface. These surface adsorbed hydrogen species readily hydrogenate adsorbed CO 2 molecules through the Langmuir-Hinshelwood mechanism. Furthermore, these surface hydrogen species can also participate in the conversion of gas-phase CO 2 molecules through the Eley-Rideal pathway. This work sheds light on the synergistic plasma catalytic mechanism and provide insights for optimizing CO 2 hydrogenation processes using MXene catalysts.
研究领域:
化学工程
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催化
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环境科学
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等离子体化学
✓ 已验证
产品关联
DOI
高影响因子
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