INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
·
2022
·
IF 4.326
Fangyi Pei,Zhimiao Wang,Jianhua Lv,Fang Li,Wei Xue
Cu–Zn–Al catalyst was prepared by the co-precipitation method, and the catalytic performance for transfer hydrogenation of acetophenone (AP) to 1-phenylethanol (1-PhE) was evaluated using isopropanol (IPA) as a hydrogen source. The addition of Zn changed the morphology of the catalyst and reduced aggregation of catalyst particles, resulting in highly dispersed Cu active sites. As the Zn content increased, the valence state of Cu species changed. When the Cu/Zn molar ratio was 2/3, the Cu+/Cu0 ratio in the catalyst was 0.81, resulting in good selectivity for 1-PhE. The reaction conditions were optimized over the Cu–Zn–Al catalyst with a Cu/Zn molar ratio of 2/3. When the reaction was performed at 180 °C for 2 h with an IPA/AP molar ratio of 15, the AP conversion was 89.4% and the 1-PhE selectivity was 93.2%. The Cu–Zn–Al catalyst showed good stability, and AP conversion and the 1-PhE selectivity were essentially unchanged after five cycles.
研究领域:
催化化学
·
有机合成
·
材料科学
✓ 已验证
DOI
高影响因子
Journal of Materials Chemistry A
·
2021
·Vol. 9
·期 42
·23817-23827
·
IF 12.732
Manman Feng,Xuemei Wu,Huiyuan Cheng,Zihao Fan,Xiangcun Li,Fujun Cui,Shuai Fan,Yan Dai,Guangping Lei,Gaohong He
The diatomic catalysts (DACs) provide a new strategy for efficient catalysis of CO2 reduction reaction (CO2RR) owing to their maximum atomic utility and more flexible active sites. However, it is still challenging to precisely design heteronuclear diatomic active centers and understand the coordination mechanism of binary sites at the atomic level. Herein, a nitrogen-doped carbon matrix with precisely controlled Fe–Cu diatom sites is synthesized through a metal–organic framework. The as-obtained Fe/Cu–N–C catalyst exhibits an excellent CO faradaic efficiency (>95% over a wide potential range of −0.4 to −1.1 V vs. RHE, 99.2% at −0.8 V vs. RHE), a high turnover frequency (5047 h−1 at −1.1 V vs. RHE), and a low overpotential (50 mV), thus outperforming most reported atomically dispersed catalysts. Further density functional theory calculations indicate that the synergy between Fe–Cu diatoms causes rapid charge transfer and effectively adjusts the position of the d-band center, which reduces the energy barriers for *COOH formation and *CO desorption. This work provides a new approach for advancing universal synthesis strategies to construct heteronuclear diatomic catalysts and explore synergistic effects.
研究领域:
材料科学
·
催化化学
·
能源转换
✓ 已验证
DOI
高影响因子
Materials Today Physics
·
2022
·
IF 11.021
X. Li,Z. Wang,J. Zhang,K. Dai,K. Fan,G. Dawson
The solar driven reduction of carbon dioxide (CO 2 ) to high value-added carbon based fuel is a promising solution to mitidate climate and energy problems, however, improving the adsorption and conversion efficiency of CO 2 in the photoreduction process still faces severe challenges. In this work, Cd 0·7 Zn 0·3 Se solid solution was prepared by cation exchange: selenium (Se) vacancies are produced during ion exchange, which promotes the unsaturated coordination of the surrounding metal atoms. The adsorption of diethylenetriamine (DETA) on the surface limits the growth of Cd x Zn 1- x Se crystallites , resulting in insufficient coordination of the surface atoms, which then become active adsorption sites. Furthermore, a heterojunction was formed with Cu 2 O@Cu to accelerate the separation and transfer of photo-induced carriers of Cd 0·7 Zn 0·3 Se, and the optimized Cd 0·7 Zn 0·3 Se/Cu 2 O@Cu (CZS/CC) step-scheme heterojunction exhibited a CO release activity of 50.5 μmol g −1 h −1 , which is 3.8 and 10.7 times higher than that of Cd 0·7 Zn 0·3 Se and Cu 2 O@Cu, respectively. This work is expected to open up new insight for the regulation of nanostructures and the design of selective catalysts.
研究领域:
材料科学
·
环境科学
✓ 已验证
DOI
高影响因子
ACS Nano
·
2024
·
IF 15.8
Minglei Lu,Zhuoyu Zheng,Weiwei Lu,Haiping Zhu,Junwei Liao,Yuxin Ge,Xueer Huang,Qian Zhang,Jiajin Li,Yiyuan Zhou,Xiaoping Wu,Baozhu Chen,Chunxiao Yang,Xitang Qian,Minhua Shao,Tiejun Wang
Aqueous-phase reforming of methanol represents a promising avenue for hydrogen (H2) production. However, developing highly efficient and low-cost nonprecious catalysts remains challenging. Here, we report the synthesis of Cu-based catalysts with Cu, Cu2O, and CuN3 nanoparticles anchored on the nitrogen-doped carbon, forming Cu0/Cu+/Cu-N3 active sites. This catalyst achieves a H2 production rate of 140.1 μmol/gcat/s at 210 °C, which is several times to 2 orders of magnitude higher than that of Cu-, Ni-, even Pt-based catalysts, demonstrating excellent long-term stability over 350 h at 210 °C. A mechanism investigation reveals that the Cu-N3 site facilitates water dissociation into *OH and improves *CO and *OH conversion, leading to enhanced CO conversion and H2 production kinetics.
研究领域:
催化化学
·
能源材料科学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
Chem Catalysis
·
2022
·
IF 0
Wenjie Wu,Yulu Yang,Yitong Wang,Tiantian Lu,Qingsong Dong,Junwei Zhao,Jingyang Niu,Qingchao Liu,Zhaomin Hao,Shuyan Song
Electrosynthesis of urea from N 2 and CO 2 molecules is of immense significance but has so far been plagued by the lack of a universal design principle to guide the search for new catalysts. Herein, as exemplified by the Cu-Bi catalyst, our findings revealed that the defective Cu-Bi catalyst could offer a maximum urea concentration of 0.45 ± 0.06 mg L −1 and the largest faradaic efficiency of 8.7% ± 1.7% at −0.4 V (versus reversible hydrogen electrode [RHE]), exhibiting outstanding activity in contrast to monometallic (Cu and Bi) and bimetallic (Cu-Bi mixture and intact Cu-Bi) catalysts. Moreover, the evidence from isotope tracing experiments, in situ Raman spectroscopy, and density functional theory (DFT) calculations suggested that it is a promising strategy for the co-reduction of N 2 and CO 2 by defective Cu-Bi catalysts, switching on a light to the application of defects in electrosynthesis of urea.
研究领域:
化学工程
·
材料科学
·
催化反应
✓ 已验证
DOI
APPLIED SURFACE SCIENCE
·
2024
·
IF 6.3
Huijuan Chen,Fangrui Gao,Wenbin Ren,Lulu Du,Kaifeng Xue,Pinhua Zhang,Changmin Shi,Li Lv,Guangliang Cui
Ultra-sensitive hydrogen sulfide (H 2 S) detection technology at low temperatures provides critical support for the application of one-time alert systems under extreme conditions, ensuring reliable monitoring of H 2 S in low-temperature environments and enhancing safety and practicability. In this study, we developed a novel low-temperature H 2 S sensor based on Cu/Cu 2 O nanoarrays, prepared through a combination of 2D electrodeposition in situ assembly and the hydrothermal method. The heterointerface between Cu nanowires and Cu 2 O nanocubes presents a high barrier, which can be modulated to zero through the formation of continuous Cu x S conductive channels via the vulcanization reaction, thereby achieving excellent sensitivity and selectivity towards H 2 S at low temperatures. At freezing temperatures and low H 2 S concentrations (≤20 ppm), the sensors show ideal recovery and reasonable sensitivity (R=150 to 10 ppm H 2 S at 0 °C). However, the response significantly increases (R=5624 at 10 ppm H 2 S at 50 °C) and recovery is lost under reversed conditions. First-principles calculations have confirmed that the enhanced H 2 S adsorption at the heterointerface is the primary reason for the robust response observed at 0 °C. Experimental results demonstrate that the Cu/Cu 2 O nanoarrays were capable of rapid detection of H 2 S at low temperatures through modulation of heterointerface barriers.
研究领域:
材料科学
·
化学传感器
·
表面科学
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF MATERIALS SCIENCE
·
2020
·Vol. 55
·期 24
·10388-10398
·
IF 3.553
Zhong Mingjun,Zhang Shizhen,Dong Anwang,Sui Zhuyin,Feng Lijuan,Chen Qi
Heterogeneous metal–organic framework composites are widely used to catalyze the synthesis reaction of organic materials. Here, we report the use of a heterogeneous catalyst to catalyze the reaction of alcohols and amines to synthesize imines directly using a one-pot method. A low-dimensional Cu-MOF prepared by a simple surfactant-assisted method shows the morphology of nanorods. Cu-MOF nanorods provide an ideal support for preparing supported metal nanocatalysts. A reduction method was applied to immobilize the ultrafine noble metal Au and Pd nanoparticles on the surface of Cu-MOF nanorods to form a Cu-MOF/Au–Pd composite catalyst. Cu-MOF/Au–Pd catalyst is used to catalyze the reaction between alcohols and amines to form imines. Due to the synergy between different metal nanoparticles, it can effectively catalyze the reaction to form imines. In addition, Cu 2+ in Cu-MOF/Au–Pd catalyst facilitates the adsorption of substances by excess electrons and promotes product formation. After 12 h of catalytic reaction, the yield of imine is as high as 95%.
研究领域:
催化
·
材料科学
·
化学工程
✓ 已验证
DOI
高影响因子
CATALYSIS COMMUNICATIONS
·
2008
·
IF 2.394
Yunlai Ren,Zhifei Liu,Shuang Zhao,Xinzhe Tian,Jianji Wang,Weiping Yin,Shebin He
Commercially available and inexpensive ethylenediamine/Cu(OAc) 2 · H 2 O has been found to be a highly effective catalyst system for the cyanation of aryl bromides in the solvent of NMP. At the same time, the highly activated aryl chlorides with NO 2 groups gave corresponding benzonitriles in good yields. Similar to the previous observation, it is not necessary to use an excess of K 4 [Fe(CN) 6 ] in the cyanation reaction (only 20 mol% of K 4 [Fe(CN) 6 ] was used). In other hand, a more remarkable KI-accelerated effect was observed for the cyanation reaction: the addition of KI increased the yield from 6% to 91% in the cyanation of bromobenzene.
研究领域:
有机化学
·
催化化学
✓ 已验证
DOI
高影响因子
Nanomaterials
·
2021
·Vol. 11
·期 5
·1097
·
IF 5.076
Luran Zhang,Xinchen Du,Hongjie Lu,Dandan Gao,Huan Liu,Qilong Lin,Yongze Cao,Jiyang Xie,Wanbiao Hu
L10ordered FePt and FePtCu nanoparticles (NPs) with a good dispersion were successfully fabricated by a simple, green, one-step solid-phase reduction method. Fe (acac)3, Pt (acac)2, and CuO as the precursors were dispersed in NaCl and annealed at different temperatures with an H2-containing atmosphere. As the annealing temperature increased, the chemical order parameter (S), average particle size (D), coercivity (Hc), and saturation magnetization (Ms) of FePt and FePtCu NPs increased and the size distribution range of the particles became wider. The ordered degree,D,Hc, andMsof FePt NPs were greatly improved by adding 5% Cu. The highestS,D,Hc, andMswere obtained when FePtCu NPs annealed at 750 °C, which were 0.91, 4.87 nm, 12,200 Oe, and 23.38 emu/g, respectively. The structure and magnetic properties of FePt and FePtCu NPs at different annealing temperatures were investigated and the formation mechanism of FePt and FePtCu NPs were discussed in detail.
研究领域:
材料科学
·
物理学
✓ 已验证
DOI
高影响因子
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
·
2025
·
IF 3.9
Shan Li,Huixia Li,Taotao Huang,Xuebo Chen
The development of efficient Cu–Ce catalysts for selective CO oxidation in hydrogen streams (CO-PROX) remains a critical challenge for hydrogen purification technologies. Herein, we report an acid-modified Cu–Ce/γ-Al2O3 catalyst synthesized through HCl-assisted wet impregnation and thermal aging, demonstrating exceptional low-temperature CO-PROX performance. The optimized CuCe0.8(Cl)0.2/γ-Al2O3 catalyst achieves superior CO conversion below 160 °C and maintains stable activity for 50 h at 160 °C. Mechanistic studies reveal that HCl modification induces dual enhancement effects: (1) increased Cu+ species density enhances CO adsorption capacity; (2) elevated Ce3+ concentration promotes oxygen vacancy formation for efficient O2 activation. Complementary characterization demonstrates that the acid treatment optimizes the active species dispersion and creates hierarchical pore structures in the γ-Al2O3 support, which facilitates reactant accessibility and stabilizes catalytic intermediates. The reaction mechanism involves synergistic cooperation between Cu+-mediated CO adsorption, oxygen vacancy-assisted O2 activation, and hydroxyl-assisted bicarbonate intermediate formation on the alumina support. This work establishes an effective acid-modification strategy for designing durable CO-PROX catalysts, advancing the development of a practical hydrogen purification system.
研究领域:
催化化学
·
材料科学
·
环境科学
·
能源技术
✓ 已验证
产品关联
DOI
高影响因子
APPLIED SURFACE SCIENCE
·
2024
·
IF 6.3
Songhao Yu,Guifen Tian,Liduan Li,Fei Wang,Kefeng Wang,Junyu Lei,Haijun Hao,Qinghong Xu
TpFO-PA, a novel spherical hollow mesoporous polyamide, was firstly synthesized by the reaction among 1,3,5-tris(4-aminophenyl)benzene (TAPB), furylamine and oxalyl chloride in using silica-gel nanoparticle as hard template, and the composite Cu(I)@TpFO-PA with high catalytic activities in C-N coupling reactions between (hetero)aryl bromide and (hetero)aryl amines under mild conditions was prepared basing on presence of N in the framework. A maximum activity of the catalyst with yield of C-N coupling product were about 311.9 g (product) /mol Cu(I) ·h and 95 % respectively, and the activity could be maintained at least 5 times after the catalyst was reused. The composite Cu(I)@TpFO-PA is a few heterogeneous catalysts reported in catalyzing coupling reaction between aromatic amines and brominated aromatic compounds.
研究领域:
化学
·
材料科学
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2022
·
IF 6.371
Guannan Yang,Pengyu Wang,Yu Liu,Shuzhou Lu,Bo Luo,Tao Lai,Shiwo Ta,Tingyu Lin,Jiye Luo,Yu Zhang,Chengqiang Cui
Ag-coated Cu particles (Cu@Ag particles) are highly anticipated bimetallic materials with wide electronic applications. However, it is still crucially challenging to obtain well-covered Ag shells and facilitate the synthetic process, and the sintering/migration behaviors of Cu@Ag particles are also poorly understood. In this study, we develop a facile Ag coating method for Cu@Ag particles with the assistance of double complexing agents. Electrochemical analysis reveals that the complexing effect can effectively reduce the potential difference of the Cu-Ag replacement reaction, and thereby improve the coating quality. Cu@Ag particles with compact and uniform Ag shells are obtained, with Ag contents as low as ~10 at%. The as-prepared Cu@Ag particles show significantly improved oxidation resistance and reliable sintering property. Moreover, the Cu@Ag particles exhibit superior ion migration resistance even better than both Cu and Ag particles under an oxygen-containing environment. The results could provide helpful basis for understanding the synthesis, sintering and migration processes of Cu@Ag particles. The comprehensive performance of Cu@Ag particles makes them a promising interconnected material in future electronic industry.
研究领域:
材料科学
·
电子工程
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）