Efficient electrocatalytic rupture of energy-rich molecules(H_(2)and O_(2))is a green approach for gener-ating clean energy for modern societies.In this context,porphyry-type molecular electrocatalysts act intelligent...Efficient electrocatalytic rupture of energy-rich molecules(H_(2)and O_(2))is a green approach for gener-ating clean energy for modern societies.In this context,porphyry-type molecular electrocatalysts act intelligently toward oxygen reduction reaction(ORR),a fundamental process in fuel cells,due to their redox-rich chemistry,which involves core metal ions and macrocyclic ligands.The concerned scientific community has tried many times to correlate the ORR intermediates with their formation kinetics and simplify the associated multi H+/e-stages during the ORR process,constructing several volcano plots be-tween catalytic Tafel data,turnover frequencies,and overpotentials for many electrocatalysts.Despite the fact that many review articles on molecular electrocatalysts for ORR have been published,understanding the strategic implications and molecular catalyst intelligence towards homogenous ORR has been poorly explored.This review examined the relationships between volcano plots of current vs.thermodynamic parameters and the Sabatier principle in order to explain the intelligence of molecular electrocatalysts and approaches for their creation,as well as the difficulties and potential prospects of molecular electro-catalysts.These facts distinguish this review from previously published articles and will pique the scien-tific community’s interest in avoiding trial-and-error procedures for catalyst creation while also allowing for more exact evaluations of the molecular catalyst’s performance.展开更多
Efficient charge carrier transfer from light harvesters to catalysts greatly determines the photocatalytic activity in an artificial photosynthesis(AP) system for solar hydrogen evolution.In this study,an AP system co...Efficient charge carrier transfer from light harvesters to catalysts greatly determines the photocatalytic activity in an artificial photosynthesis(AP) system for solar hydrogen evolution.In this study,an AP system composed of xanthene dye as light harvester and cobaloxime molecular complex as catalyst,with TiO2 as electron relay,was designed for photocatalytic hydrogen evolution under visible light(λ>420 nm).It was demonstrated that with cobaloxime molecule covalently linked onto the TiO2 electron relay,the resulting hybrid AP system exhibited much increased photocatalytic activity as compared to that without TiO2.The greatly increased photocatalytic activity should be due to the efficient electron transfer from xanthene dye as light harvester and cobaloxime molecular complex as catalyst,shuttled by the TiO2 electron relay,for the following water reduction reaction.The present study demonstrates a facile and feasible strategy to guide the design of high performance AP systems through the electron relay shuttled and promoted cha rge transfer process.展开更多
The concept of liquid-solid hybrid catalyst that featuring a truly homogeneous liquid microenvironment together with insoluble solid characteristics has been established recently by our group,which enables us to conve...The concept of liquid-solid hybrid catalyst that featuring a truly homogeneous liquid microenvironment together with insoluble solid characteristics has been established recently by our group,which enables us to conveniently bridge the gap between homo-and heterogeneous catalysis.In this study,we extend this general concept to the confinement of molecular rhodium phosphine complexes,including Rh-TPPTS,Rh-TPPMS and Rh-SXP,for olefin hydroformylation reactions.A series of hybrid catalyst materials consisting a modulated liquid interior([BMIM]NTf_(2),[BMIM]PF_(6),[BMIM]BF_(4) or H_(2)O)and a permeable silica crust were fabricated through our developed Pickering emulsion-based method,showing 9.4–24.2-fold activity enhancement and significantly improved aldehyde selectivity(from 72.2%,61.8%to 86.6%)compared to their biphasic counterparts or traditional supported liquid phase system in the hydroformylation of 1-dodecene.Interestingly,the catalytic efficiency was demonstrated to be tunable by rationally engineering the thickness of porous crust and dimensions of the liquid pool.The thus-attained hybrid catalyst could also successfully catalyze the hydroformylation of a variety of olefin substrates and be recycled without a significant loss of activity for at least seven times.展开更多
The development of inexpensive artificial photosynthetic(AP)systems,utilizing low-energy sunlight for CO_(2)reduction remains a significant challenge.Here,we report a red-light-driven CO_(2)reduction system with pyrid...The development of inexpensive artificial photosynthetic(AP)systems,utilizing low-energy sunlight for CO_(2)reduction remains a significant challenge.Here,we report a red-light-driven CO_(2)reduction system with pyridinethiolate-capped CdSe quantum dots(QDs)as the photosensitizers and a cobalt quarterpyridyl complex as the catalyst.This system,assembled from abundant elements,achieved efficient CO_(2)conversion to CO with over 97%selectivity and turnover numbers of 392 for cobalt and 7840 for QDs in aqueous solution.Over 92%selectivity was observed even at CO_(2)concentration as low as 1%,which showed potential for practical applications.To our knowledge,this is the first report of red-lightdriven CO_(2)photoreduction in QDs/catalyst-based photocatalytic systems.展开更多
Molecules with metal-N_(4) centers have been widely applied as efficient catalysts in electrocatalytic CO_(2) reduction(ECR)to CO.However,the localized d orbitals of the metal centers significantly hindered the mass a...Molecules with metal-N_(4) centers have been widely applied as efficient catalysts in electrocatalytic CO_(2) reduction(ECR)to CO.However,the localized d orbitals of the metal centers significantly hindered the mass and electron transfer of the CO_(2)-to-CO process.Herein,we propose aπ-d interaction regulation strategy that involves tuning the molecular conjugated structure to delocalize the metal d orbital of Co-N_(4)-centered molecular catalysts for ECR.The cobalt naphthalocyanine(CoNPc)with an extended conjugated structure exhibits a superior ECR performance compared to cobalt phthalocyanine(CoPc)and cobalt octaethylporphyrin(CoOEP),with the highest CO faradaic efficiency(FECO),reaching 96.1%at−0.8 V versus reversible hydrogen electrode in an H-cell and 97%at 100 mA cm^(−2) in flow cell using a bicarbonate electrolyte.Furthermore,the electrochemical scanning tunneling microscopy and theoretical analyses reveal that the extended conjugated structures promoted CO_(2) adsorption and CO desorption on Co-N_(4) active sites,thus accelerating the ECR process.These results provide insights into the design of high-performance metal-N_(4)-centered electrocatalysts.展开更多
Efficient and selective oxygen reduction reaction(ORR)electrocatalysts are critical to realizing decentralized H_(2)O_(2)production and utilization.Here we demonstrate a facile interfacial engineering strategy using a...Efficient and selective oxygen reduction reaction(ORR)electrocatalysts are critical to realizing decentralized H_(2)O_(2)production and utilization.Here we demonstrate a facile interfacial engineering strategy using a hydrophobic ionic liquid(IL,i.e.,[BMIM][NTF2])to boost the performance of a nitrogen coordinated single atom cobalt catalyst(i.e.),cobalt phthalocyanine(CoPc)supported on carbon nanotubes(CNTs).We find a strong correlation between the ORR performance of CoPc/CNT and the thickness of its IL coatings.Detailed characterization revealed that a higher O_(2)solubility(2.12×10^(−3)mol/L)in the IL compared to aqueous electrolytes provides a local O2 enriched surface layer near active catalytic sites,enhancing the ORR thermodynamics.Further,the hydrophobic IL can efficiently repel the as‐synthesized H_(2)O_(2)molecules from the catalyst surface,preventing their fast decomposition to H_(2)O,resulting in improved H_(2)O_(2)selectivity.Compared to CoPc/CNT without IL coatings,the catalyst with an optimal~8 nm IL coating can deliver a nearly 4 times higher mass specific kinetic current density and 12.5%higher H2O2 selectivity up to 92%.In a two‐electrode electrolyzer test,the optimal catalyst exhibits an enhanced productivity of 3.71 molH2O2 gcat^(–1)h^(–1),and robust stability.This IL‐based interfacial engineering strategy may also be extended to many other electrochemical reactions by carefully tailoring the thickness and hydrophobicity of IL coatings.展开更多
Electrochemical CO_(2) reduction reaction(CO_(2)RR)into value-added chemicals/fuels is crucial for realizing the sustainable carbon cycle while mitigating the energy crisis.However,it is impeded by the relatively high...Electrochemical CO_(2) reduction reaction(CO_(2)RR)into value-added chemicals/fuels is crucial for realizing the sustainable carbon cycle while mitigating the energy crisis.However,it is impeded by the relatively high overpotential and low energy efficiency due to the lack of efficient electrocatalysts.Herein,we develop an isolated single-atom Ni catalyst regulated strategy to activate and stabilize the iron phthalocyanine molecule(Ni SA@FePc)toward a highly efficient CO_(2)RR process at low overpotential.The well-defined and homogenous catalytic centers with unique structures confer Ni SA@FePc with a significantly enhanced CO_(2)RR performance compared to single-atom Ni catalyst and FePc molecule and afford the atomic understanding on active sites and catalytic mechanism.As expected,Ni SA@FePc exhibits a high selectivity of more significant Faraday efficiency(≥95%)over a wide potential range,a high current density of~252 mA·cm^(−2) at low overpotential(390 mV),and excellent long-term stability for CO_(2)RR to CO.X-ray absorption spectroscopy measurement and theoretical calculation indicate the formation of NiN_(4)-O_(2)-FePc heterogeneous structure for Ni SA@FePc.And CO_(2)RR prefers to occur at the raised N centers of NiN4-O_(2)-FePc heterogeneous structure for Ni SA@FePc,which enables facilitated adsorption of*COOH and desorption of CO,and thus accelerated overall reaction kinetics.展开更多
Electrocatalytic ammonia oxidation reaction(eAOR)is of significance to ammonia fuel economy and the production of valuable N-containing products,such as nitrite,nitrate and hydrazine.The study of well-defined molecula...Electrocatalytic ammonia oxidation reaction(eAOR)is of significance to ammonia fuel economy and the production of valuable N-containing products,such as nitrite,nitrate and hydrazine.The study of well-defined molecular catalysts offers rich insights in terms of the detailed mechanism of ammonia oxidation.This review analyzes the thermodynamics of ammonia oxidation reactions and summarizes the current progress in molecular electrocatalysts in this booming field.We emphasized the factors that influence the selectivity of products and further discussed the challenges in designing efficient catalysts.展开更多
Molecular copper catalysts serve as exemplary models for correlating the structure-reaction-mechanism relationship in the electrochemical CO_(2) reduction(eCO_(2)R),owing to their adaptable environments surrounding th...Molecular copper catalysts serve as exemplary models for correlating the structure-reaction-mechanism relationship in the electrochemical CO_(2) reduction(eCO_(2)R),owing to their adaptable environments surrounding the copper metal centres.This investigation,employing density functional theory calculations,focuses on a novel family of binuclear Cu molecular catalysts.The modulation of their coordination configuration through the introduction of organic groups aims to assess their efficacy in converting CO_(2) to C_(2)products.Our findings highlight the crucial role of chemical valence state in shaping the characteristics of binuclear Cu catalysts,consequently influencing the eCO_(2)R behaviour,Notably,the Cu(Ⅱ)Cu(Ⅱ)macrocycle catalyst exhibits enhanced suppression of the hydrogen evolution reaction(HER),facilitating proton trans fer and the eCO_(2)R process.Fu rthermore,we explo re the impact of diverse electro n-withdrawing and electron-donating groups coordinated to the macrocycle(R=-F,-H,and-OCH_3)on the electron distribution in the molecular catalysts.Strategic placement of-OCH_3 groups in the macrocycles leads to a favourable oxidation state of the Cu centres and subsequent C-C coupling to form C_(2) products.This research provides fundamental insights into the design and optimization of binuclear Cu molecular catalysts for the electrochemical conversion of CO_(2) to value-added C_(2) products.展开更多
Photocatalytic CO_(2)reduction into chemical fuels is a promising route for alleviating the energy crisis and environmental issues.However,reported catalysts still exhibit low catalytic efficiencies,which hinders the ...Photocatalytic CO_(2)reduction into chemical fuels is a promising route for alleviating the energy crisis and environmental issues.However,reported catalysts still exhibit low catalytic efficiencies,which hinders the development of this important reaction.Herein,we report the heterogenization of a dinuclear cobalt molecular catalyst into two porous polymers(Co_(2)-P1 and Co_(2)-P2)using a covalent strategy for photocatalytic CO_(2)reduction.As a result,Co_(2)-P1 with a phenyl group as the linker exhibited high catalytic performance for the photochemical CO_(2)-to-CO conversion with a CO production rate of 568.8 mmol g-1 h-1 and turnover frequency(TOF)of 11.6 min-1(CO selectivity,95.2%).More impressively,by extending the phenyl to biphenyl linker,the resulting Co_(2)-P2 shows obviously enhanced photocatalytic efficiency for CO_(2)reduction to CO,with a record CO production rate of 1063.0 mmol g-1 h-1 and TOF of 23.6 min-1(CO selectivity,94.9%)under a laboratory light source.Furthermore,Co_(2)-P2 also shows outstanding catalytic activity for photocatalytic CO_(2)reduction under natural sunlight,with a CO production rate of 544.1 mmol g-1 h-1 and TOF of 12.1 min-1(CO selectivity,97.2%).Systematic studies demonstrated that fast electron transfer from the photosensitizer to the catalyst greatly contributes to the superior catalytic activity of Co_(2)-P2.展开更多
Catalytic conversion of bio-oil into light olefins was performed by a series of molecular sieve catalysts, including HZSM-5, MCM-41, SAPO-34 and Y-zeolite. Based on the light olefins yield and its carbon selectivity, ...Catalytic conversion of bio-oil into light olefins was performed by a series of molecular sieve catalysts, including HZSM-5, MCM-41, SAPO-34 and Y-zeolite. Based on the light olefins yield and its carbon selectivity, the production of light olefins decreased in the following order： HZSM-5〉SAPO-34〉MCM-41〉Y-zeolite. The highest olefins yield from bio-oil using HZSM- 5 catalyst reached 0.22 kg/kgbio-oil with carbon selectivity of 50.7% and a nearly complete bio-oil conversion. The reaction conditions and catalyst characterization were investigated in detail to reveal the relationship between the catalyst structure and the production of olefins. The comparison between the pyrolysis and catalytic pyrolysis of bio-oil was also performed.展开更多
Rational interface engineering via regulating the anchoring groups between molecular catalysts and light-absorbing semiconductors is essential and emergent to stabilize the semiconductor/molecular complex interaction ...Rational interface engineering via regulating the anchoring groups between molecular catalysts and light-absorbing semiconductors is essential and emergent to stabilize the semiconductor/molecular complex interaction and facilitate the photocarriers transport,thus realizing highly active and stable photoelectrochemical(PEC)water splitting.In this mini review,following a showcasing of the fundamental details of hybrid PEC systems containing semiconductor photoelectrodes and molecular catalysts for water splitting,the state-of-the-art progress of anchoring group regulation at semiconductor/molecular complex interface for efficient and stable PEC water splitting,as well as its effect on charge transfer kinetics,are comprehensively reviewed.Finally,potential research directions aimed at building high-efficiency hybrid PEC water splitting systems are summarized.展开更多
Molecular sieve catalysts,owing to their unique chemical properties,are widely used as catalysts among various catalytic reactions.Abundant Br?nsted acid sites in molecular sieve catalysts usually enable active compon...Molecular sieve catalysts,owing to their unique chemical properties,are widely used as catalysts among various catalytic reactions.Abundant Br?nsted acid sites in molecular sieve catalysts usually enable active components to disperse well on the catalyst surface,and help to adsorb a large number of gas molecules to achieve maximum catalytic performance.Therefore,a variety of molecular sieve catalysts have been developed and used in the selective catalytic reduction of NO_(x)by NH_(3)(NH_(3)-SCR).For example,Cu molecular sieve catalysts such as Cu-SSZ-13 and Cu-SAPO-34 with wide temperature windows and stable structure are considered and applied as commercial catalysts for NO_(x)removal in diesel vehicles for a long time.Although molecular sieve catalysts possess many advantages,they still cannot avoid the serious deactivation caused by various factors in practical applications.In this review,reasons leading to the deactivation of molecular sieve catalysts for NO_(x)reduction in actual working conditions were concluded.The deactivation mechanisms of molecular sieve catalysts for NO_(x)reduction were analyzed and the corresponding anti-deactivation strategies were summarized.Finally,challenges and prospects of molecular sieve catalysts for NO_(x)reduction were also proposed.展开更多
In this paper,the bi-functional catalyst system composed of molecular sieve（MCM-41） immobilized oligomerization catalyst（C25H17Cl2N3·FeCl2） and copolymerization catalyst（Et（Ind）2ZrCl2） was employed in the...In this paper,the bi-functional catalyst system composed of molecular sieve（MCM-41） immobilized oligomerization catalyst（C25H17Cl2N3·FeCl2） and copolymerization catalyst（Et（Ind）2ZrCl2） was employed in the in situ copolymerization of ethylene aiming to prepare the Linear low density polyethylene（LLDPE）.In this paper,we mainly argued the regular pattern of the in situ copolymerization of ethylene in limited nano-space and compared it with that happening in free space.The impact of variance of the reaction temperature,Fe/Zr value and the A1/（Fe＋Zr） value on the activity of the in situ copolymerization of ethylene has also been introduced.Furthermore,the degree of branching,thermal properties and crystalline changes of the obtained polymerization products prepared from different reactivity were investigated.展开更多
Bis(imino)pyridyl Fe(Ⅱ) complexes are important catalysts in ethylene oligomerization for preparingα-olefins. The metal net charge-activity relationship of bis(imino)pyridyl Fe(Ⅱ) complexes was investigated by mole...Bis(imino)pyridyl Fe(Ⅱ) complexes are important catalysts in ethylene oligomerization for preparingα-olefins. The metal net charge-activity relationship of bis(imino)pyridyl Fe(Ⅱ) complexes was investigated by molecular mechanics (MM) and net charge equilibration(QEq) method with modified Dreiding force field.It was found that metal net charge was in reverse ratio to ethylene oligomerization activity.Electron-donor substituents with less steric hindrance to the central metal were favorable to Fe complex act...展开更多
In an alkaline 2-propanol solution with 5,10,15,20-tetra(4-methoxyl phenyl) porphyrin iron chloride(TOMPPFeCl) as a catalyst and oxygen as a cheap green oxidant, 2-naphthol was conversed to 2-hydroxy-\{1,4-naphthoquin...In an alkaline 2-propanol solution with 5,10,15,20-tetra(4-methoxyl phenyl) porphyrin iron chloride(TOMPPFeCl) as a catalyst and oxygen as a cheap green oxidant, 2-naphthol was conversed to 2-hydroxy-\{1,4-naphthoquinone(HNQ)\} with a yield of 62.17% and a selectivity of 100%, and the conversion number of TMOPPFeCl catalyst was 8.32/min. The catalytic oxidation products were characterized by means of UV-Vis, IR, GC-MS, ~ 1H NMR and melting point determination. In this catalytic oxidation, the catalytic activity of TMOPPFeCl was researched in detail and the reacting conditions were optimized. A possible reaction mechanism is summarized based on in situ EPR determination.展开更多
Water oxidation, as a mandatory reaction of solar fuels conversion systems, requires the use of light absorbers with electronic properties that are well matched with those of the multi-electron catalyst in order to ac...Water oxidation, as a mandatory reaction of solar fuels conversion systems, requires the use of light absorbers with electronic properties that are well matched with those of the multi-electron catalyst in order to achieve high efficiency. Molecular light absorbers offer flexibility in fine tuning of orbital energetics,and metal oxide nanoparticles have emerged as robust oxygen evolving catalysts. Hence, these material choices offer a promising approach for the development of photocatalytic systems for water oxidation.However, efficient charge transfer coupling of molecular light absorbers and metal oxide nanoparticle catalysts has proven a challenge. Recent new approaches toward the efficient coupling of these components based on synthetic design improvements combined with direct spectroscopic observation and kinetic evaluation of charge transfer processes are discussed.展开更多
The effect of chemical composition of highly active supported Ziegler-Natta catalysts with controlled morphology on the MWD of PE has been studied.It was shown the variation of transition metal compound in the MgCl_2-...The effect of chemical composition of highly active supported Ziegler-Natta catalysts with controlled morphology on the MWD of PE has been studied.It was shown the variation of transition metal compound in the MgCl_2-supported catalyst affect of MWD of PE produced in broad range:Vanadium-magnesium catalyst(VMC)produce PE with broad and bimodal MWD(M_w/M_n=14-21).MWD of PE,produced over titanium-magnesium catalyst(TMC)is narrow or medium depending on Ti content in the catalyst(M_w/M_n=3.1-4.8).The oxidation ...展开更多
基金funding this work through large group Research Project under grant number RGP2/172/44.
文摘Efficient electrocatalytic rupture of energy-rich molecules(H_(2)and O_(2))is a green approach for gener-ating clean energy for modern societies.In this context,porphyry-type molecular electrocatalysts act intelligently toward oxygen reduction reaction(ORR),a fundamental process in fuel cells,due to their redox-rich chemistry,which involves core metal ions and macrocyclic ligands.The concerned scientific community has tried many times to correlate the ORR intermediates with their formation kinetics and simplify the associated multi H+/e-stages during the ORR process,constructing several volcano plots be-tween catalytic Tafel data,turnover frequencies,and overpotentials for many electrocatalysts.Despite the fact that many review articles on molecular electrocatalysts for ORR have been published,understanding the strategic implications and molecular catalyst intelligence towards homogenous ORR has been poorly explored.This review examined the relationships between volcano plots of current vs.thermodynamic parameters and the Sabatier principle in order to explain the intelligence of molecular electrocatalysts and approaches for their creation,as well as the difficulties and potential prospects of molecular electro-catalysts.These facts distinguish this review from previously published articles and will pique the scien-tific community’s interest in avoiding trial-and-error procedures for catalyst creation while also allowing for more exact evaluations of the molecular catalyst’s performance.
基金supported financially by the Scientific Research Program funded by Shaanxi Provincial Education Department (No. 15JK1369)。
文摘Efficient charge carrier transfer from light harvesters to catalysts greatly determines the photocatalytic activity in an artificial photosynthesis(AP) system for solar hydrogen evolution.In this study,an AP system composed of xanthene dye as light harvester and cobaloxime molecular complex as catalyst,with TiO2 as electron relay,was designed for photocatalytic hydrogen evolution under visible light(λ>420 nm).It was demonstrated that with cobaloxime molecule covalently linked onto the TiO2 electron relay,the resulting hybrid AP system exhibited much increased photocatalytic activity as compared to that without TiO2.The greatly increased photocatalytic activity should be due to the efficient electron transfer from xanthene dye as light harvester and cobaloxime molecular complex as catalyst,shuttled by the TiO2 electron relay,for the following water reduction reaction.The present study demonstrates a facile and feasible strategy to guide the design of high performance AP systems through the electron relay shuttled and promoted cha rge transfer process.
文摘The concept of liquid-solid hybrid catalyst that featuring a truly homogeneous liquid microenvironment together with insoluble solid characteristics has been established recently by our group,which enables us to conveniently bridge the gap between homo-and heterogeneous catalysis.In this study,we extend this general concept to the confinement of molecular rhodium phosphine complexes,including Rh-TPPTS,Rh-TPPMS and Rh-SXP,for olefin hydroformylation reactions.A series of hybrid catalyst materials consisting a modulated liquid interior([BMIM]NTf_(2),[BMIM]PF_(6),[BMIM]BF_(4) or H_(2)O)and a permeable silica crust were fabricated through our developed Pickering emulsion-based method,showing 9.4–24.2-fold activity enhancement and significantly improved aldehyde selectivity(from 72.2%,61.8%to 86.6%)compared to their biphasic counterparts or traditional supported liquid phase system in the hydroformylation of 1-dodecene.Interestingly,the catalytic efficiency was demonstrated to be tunable by rationally engineering the thickness of porous crust and dimensions of the liquid pool.The thus-attained hybrid catalyst could also successfully catalyze the hydroformylation of a variety of olefin substrates and be recycled without a significant loss of activity for at least seven times.
基金the financial support provided by Sun Yat-sen University,Green Biotechnologies Research Center of Excellence(GBRCE)for Functional Molecular Engineering,China,the National Natural Science Foundation of China(grant no.22471301)Guangdong Basic and Applied Basic Research Foundation,China(grant no.2024A1515011465)+1 种基金Guangzhou Science and Technology Programme,China(grant no.2024A04J6419)the China Postdoctoral Science Foundation(grant nos.2022TQ0380 and 2022M723586).
文摘The development of inexpensive artificial photosynthetic(AP)systems,utilizing low-energy sunlight for CO_(2)reduction remains a significant challenge.Here,we report a red-light-driven CO_(2)reduction system with pyridinethiolate-capped CdSe quantum dots(QDs)as the photosensitizers and a cobalt quarterpyridyl complex as the catalyst.This system,assembled from abundant elements,achieved efficient CO_(2)conversion to CO with over 97%selectivity and turnover numbers of 392 for cobalt and 7840 for QDs in aqueous solution.Over 92%selectivity was observed even at CO_(2)concentration as low as 1%,which showed potential for practical applications.To our knowledge,this is the first report of red-lightdriven CO_(2)photoreduction in QDs/catalyst-based photocatalytic systems.
基金the National Key Research and Development Program of China(grant no.2023YFA1500014)the National Natural Science Foundation of China(grant nos.22025208,22102191,and 22432006).The authors also acknowledge the financial support of the Chinese Academy of Sciences.
文摘Molecules with metal-N_(4) centers have been widely applied as efficient catalysts in electrocatalytic CO_(2) reduction(ECR)to CO.However,the localized d orbitals of the metal centers significantly hindered the mass and electron transfer of the CO_(2)-to-CO process.Herein,we propose aπ-d interaction regulation strategy that involves tuning the molecular conjugated structure to delocalize the metal d orbital of Co-N_(4)-centered molecular catalysts for ECR.The cobalt naphthalocyanine(CoNPc)with an extended conjugated structure exhibits a superior ECR performance compared to cobalt phthalocyanine(CoPc)and cobalt octaethylporphyrin(CoOEP),with the highest CO faradaic efficiency(FECO),reaching 96.1%at−0.8 V versus reversible hydrogen electrode in an H-cell and 97%at 100 mA cm^(−2) in flow cell using a bicarbonate electrolyte.Furthermore,the electrochemical scanning tunneling microscopy and theoretical analyses reveal that the extended conjugated structures promoted CO_(2) adsorption and CO desorption on Co-N_(4) active sites,thus accelerating the ECR process.These results provide insights into the design of high-performance metal-N_(4)-centered electrocatalysts.
文摘Efficient and selective oxygen reduction reaction(ORR)electrocatalysts are critical to realizing decentralized H_(2)O_(2)production and utilization.Here we demonstrate a facile interfacial engineering strategy using a hydrophobic ionic liquid(IL,i.e.,[BMIM][NTF2])to boost the performance of a nitrogen coordinated single atom cobalt catalyst(i.e.),cobalt phthalocyanine(CoPc)supported on carbon nanotubes(CNTs).We find a strong correlation between the ORR performance of CoPc/CNT and the thickness of its IL coatings.Detailed characterization revealed that a higher O_(2)solubility(2.12×10^(−3)mol/L)in the IL compared to aqueous electrolytes provides a local O2 enriched surface layer near active catalytic sites,enhancing the ORR thermodynamics.Further,the hydrophobic IL can efficiently repel the as‐synthesized H_(2)O_(2)molecules from the catalyst surface,preventing their fast decomposition to H_(2)O,resulting in improved H_(2)O_(2)selectivity.Compared to CoPc/CNT without IL coatings,the catalyst with an optimal~8 nm IL coating can deliver a nearly 4 times higher mass specific kinetic current density and 12.5%higher H2O2 selectivity up to 92%.In a two‐electrode electrolyzer test,the optimal catalyst exhibits an enhanced productivity of 3.71 molH2O2 gcat^(–1)h^(–1),and robust stability.This IL‐based interfacial engineering strategy may also be extended to many other electrochemical reactions by carefully tailoring the thickness and hydrophobicity of IL coatings.
基金supported by the National Natural Science Foundation of China(No.21725103)National Key R&D Program of China(No.2019YFA0705704)+4 种基金the Strategic Priority Research Program of the Chinese Academy of Sciences(No.XDA21010210)Jilin Province Science and Technology Development Plan Funding Project(No.20200201079JC)Changchun Science and Technology Development Plan Funding Project(No.19SS010)Jilin Province Capital Construction Funds Project(No.2020C026-1)the K.C.Wong Education Foundation(No.GJTD-2018-09).
文摘Electrochemical CO_(2) reduction reaction(CO_(2)RR)into value-added chemicals/fuels is crucial for realizing the sustainable carbon cycle while mitigating the energy crisis.However,it is impeded by the relatively high overpotential and low energy efficiency due to the lack of efficient electrocatalysts.Herein,we develop an isolated single-atom Ni catalyst regulated strategy to activate and stabilize the iron phthalocyanine molecule(Ni SA@FePc)toward a highly efficient CO_(2)RR process at low overpotential.The well-defined and homogenous catalytic centers with unique structures confer Ni SA@FePc with a significantly enhanced CO_(2)RR performance compared to single-atom Ni catalyst and FePc molecule and afford the atomic understanding on active sites and catalytic mechanism.As expected,Ni SA@FePc exhibits a high selectivity of more significant Faraday efficiency(≥95%)over a wide potential range,a high current density of~252 mA·cm^(−2) at low overpotential(390 mV),and excellent long-term stability for CO_(2)RR to CO.X-ray absorption spectroscopy measurement and theoretical calculation indicate the formation of NiN_(4)-O_(2)-FePc heterogeneous structure for Ni SA@FePc.And CO_(2)RR prefers to occur at the raised N centers of NiN4-O_(2)-FePc heterogeneous structure for Ni SA@FePc,which enables facilitated adsorption of*COOH and desorption of CO,and thus accelerated overall reaction kinetics.
基金supported by the National Key R&D Program of China(2022YFC3401802)the National Natural Science Foundation of China(22279105)+4 种基金the Zhejiang Provincial Natural Science Foundation(XHD24B0201)the Starting-up Package from Westlake Universitythe Kunpeng Research Fund from Zhejiang ProvinceResearch Center for Industries of the FutureZhejiang Baima Lake Laboratory。
文摘Electrocatalytic ammonia oxidation reaction(eAOR)is of significance to ammonia fuel economy and the production of valuable N-containing products,such as nitrite,nitrate and hydrazine.The study of well-defined molecular catalysts offers rich insights in terms of the detailed mechanism of ammonia oxidation.This review analyzes the thermodynamics of ammonia oxidation reactions and summarizes the current progress in molecular electrocatalysts in this booming field.We emphasized the factors that influence the selectivity of products and further discussed the challenges in designing efficient catalysts.
基金the HUST-QMUL Strategic Partnership Research Funding(No.2022-HUST-QMUL-SPRF-03),which funded the project“Design of Binuclear Copper Electrocatalysts for CO_(2) Conversion from First Principles”the China Scholarship Council for financial support。
文摘Molecular copper catalysts serve as exemplary models for correlating the structure-reaction-mechanism relationship in the electrochemical CO_(2) reduction(eCO_(2)R),owing to their adaptable environments surrounding the copper metal centres.This investigation,employing density functional theory calculations,focuses on a novel family of binuclear Cu molecular catalysts.The modulation of their coordination configuration through the introduction of organic groups aims to assess their efficacy in converting CO_(2) to C_(2)products.Our findings highlight the crucial role of chemical valence state in shaping the characteristics of binuclear Cu catalysts,consequently influencing the eCO_(2)R behaviour,Notably,the Cu(Ⅱ)Cu(Ⅱ)macrocycle catalyst exhibits enhanced suppression of the hydrogen evolution reaction(HER),facilitating proton trans fer and the eCO_(2)R process.Fu rthermore,we explo re the impact of diverse electro n-withdrawing and electron-donating groups coordinated to the macrocycle(R=-F,-H,and-OCH_3)on the electron distribution in the molecular catalysts.Strategic placement of-OCH_3 groups in the macrocycles leads to a favourable oxidation state of the Cu centres and subsequent C-C coupling to form C_(2) products.This research provides fundamental insights into the design and optimization of binuclear Cu molecular catalysts for the electrochemical conversion of CO_(2) to value-added C_(2) products.
基金supported by National Key R&D Program of China(grant no.2022YFA1502902)the National Natural Science Foundation of China(grant nos.22371208,22271218,22071182,and 21931007)the Science&Technology Development Fund of Tianjin Education Commission for Higher Education(grant no.2018KJ129).
文摘Photocatalytic CO_(2)reduction into chemical fuels is a promising route for alleviating the energy crisis and environmental issues.However,reported catalysts still exhibit low catalytic efficiencies,which hinders the development of this important reaction.Herein,we report the heterogenization of a dinuclear cobalt molecular catalyst into two porous polymers(Co_(2)-P1 and Co_(2)-P2)using a covalent strategy for photocatalytic CO_(2)reduction.As a result,Co_(2)-P1 with a phenyl group as the linker exhibited high catalytic performance for the photochemical CO_(2)-to-CO conversion with a CO production rate of 568.8 mmol g-1 h-1 and turnover frequency(TOF)of 11.6 min-1(CO selectivity,95.2%).More impressively,by extending the phenyl to biphenyl linker,the resulting Co_(2)-P2 shows obviously enhanced photocatalytic efficiency for CO_(2)reduction to CO,with a record CO production rate of 1063.0 mmol g-1 h-1 and TOF of 23.6 min-1(CO selectivity,94.9%)under a laboratory light source.Furthermore,Co_(2)-P2 also shows outstanding catalytic activity for photocatalytic CO_(2)reduction under natural sunlight,with a CO production rate of 544.1 mmol g-1 h-1 and TOF of 12.1 min-1(CO selectivity,97.2%).Systematic studies demonstrated that fast electron transfer from the photosensitizer to the catalyst greatly contributes to the superior catalytic activity of Co_(2)-P2.
基金V. ACKNOWLEDGEMENTS This work was supported by the National Natural Science Foundation of China （No.51161140331） and the National High Technology Research and Development of Ministry of Science and Technology of China （No.2009AA05Z435）.
文摘Catalytic conversion of bio-oil into light olefins was performed by a series of molecular sieve catalysts, including HZSM-5, MCM-41, SAPO-34 and Y-zeolite. Based on the light olefins yield and its carbon selectivity, the production of light olefins decreased in the following order： HZSM-5〉SAPO-34〉MCM-41〉Y-zeolite. The highest olefins yield from bio-oil using HZSM- 5 catalyst reached 0.22 kg/kgbio-oil with carbon selectivity of 50.7% and a nearly complete bio-oil conversion. The reaction conditions and catalyst characterization were investigated in detail to reveal the relationship between the catalyst structure and the production of olefins. The comparison between the pyrolysis and catalytic pyrolysis of bio-oil was also performed.
基金support of the Natural Science Foundation of Shaanxi Province(2023-JC-QN-0415)the Special Project on Functional Materials from Shaanxi Provincial Department of Finance(0801YC2305)+1 种基金the Talent Project from Northwest Institute for Non-ferrous Metal Research(YK2310)the National Natural Science Foundation of China(52225606 and 52304334).
文摘Rational interface engineering via regulating the anchoring groups between molecular catalysts and light-absorbing semiconductors is essential and emergent to stabilize the semiconductor/molecular complex interaction and facilitate the photocarriers transport,thus realizing highly active and stable photoelectrochemical(PEC)water splitting.In this mini review,following a showcasing of the fundamental details of hybrid PEC systems containing semiconductor photoelectrodes and molecular catalysts for water splitting,the state-of-the-art progress of anchoring group regulation at semiconductor/molecular complex interface for efficient and stable PEC water splitting,as well as its effect on charge transfer kinetics,are comprehensively reviewed.Finally,potential research directions aimed at building high-efficiency hybrid PEC water splitting systems are summarized.
基金the support from the National Natural Science Foundation of China(No.22125604)the Chenguang Program supported by Shanghai Education Development Foundation and Shanghai Municipal Education Commission(No.22Z00354)。
文摘Molecular sieve catalysts,owing to their unique chemical properties,are widely used as catalysts among various catalytic reactions.Abundant Br?nsted acid sites in molecular sieve catalysts usually enable active components to disperse well on the catalyst surface,and help to adsorb a large number of gas molecules to achieve maximum catalytic performance.Therefore,a variety of molecular sieve catalysts have been developed and used in the selective catalytic reduction of NO_(x)by NH_(3)(NH_(3)-SCR).For example,Cu molecular sieve catalysts such as Cu-SSZ-13 and Cu-SAPO-34 with wide temperature windows and stable structure are considered and applied as commercial catalysts for NO_(x)removal in diesel vehicles for a long time.Although molecular sieve catalysts possess many advantages,they still cannot avoid the serious deactivation caused by various factors in practical applications.In this review,reasons leading to the deactivation of molecular sieve catalysts for NO_(x)reduction in actual working conditions were concluded.The deactivation mechanisms of molecular sieve catalysts for NO_(x)reduction were analyzed and the corresponding anti-deactivation strategies were summarized.Finally,challenges and prospects of molecular sieve catalysts for NO_(x)reduction were also proposed.
基金Supported by the National "Eleventh Five-Year" Technology Support Program Project (2006BAD10B08)Natural Science Foundation of Hebei Province (E2009000448)
文摘In this paper,the bi-functional catalyst system composed of molecular sieve（MCM-41） immobilized oligomerization catalyst（C25H17Cl2N3·FeCl2） and copolymerization catalyst（Et（Ind）2ZrCl2） was employed in the in situ copolymerization of ethylene aiming to prepare the Linear low density polyethylene（LLDPE）.In this paper,we mainly argued the regular pattern of the in situ copolymerization of ethylene in limited nano-space and compared it with that happening in free space.The impact of variance of the reaction temperature,Fe/Zr value and the A1/（Fe＋Zr） value on the activity of the in situ copolymerization of ethylene has also been introduced.Furthermore,the degree of branching,thermal properties and crystalline changes of the obtained polymerization products prepared from different reactivity were investigated.
基金supported by the National Science Foundation of China(Nos20334030,50703044 and 20734002)
文摘Bis(imino)pyridyl Fe(Ⅱ) complexes are important catalysts in ethylene oligomerization for preparingα-olefins. The metal net charge-activity relationship of bis(imino)pyridyl Fe(Ⅱ) complexes was investigated by molecular mechanics (MM) and net charge equilibration(QEq) method with modified Dreiding force field.It was found that metal net charge was in reverse ratio to ethylene oligomerization activity.Electron-donor substituents with less steric hindrance to the central metal were favorable to Fe complex act...
文摘In an alkaline 2-propanol solution with 5,10,15,20-tetra(4-methoxyl phenyl) porphyrin iron chloride(TOMPPFeCl) as a catalyst and oxygen as a cheap green oxidant, 2-naphthol was conversed to 2-hydroxy-\{1,4-naphthoquinone(HNQ)\} with a yield of 62.17% and a selectivity of 100%, and the conversion number of TMOPPFeCl catalyst was 8.32/min. The catalytic oxidation products were characterized by means of UV-Vis, IR, GC-MS, ~ 1H NMR and melting point determination. In this catalytic oxidation, the catalytic activity of TMOPPFeCl was researched in detail and the reacting conditions were optimized. A possible reaction mechanism is summarized based on in situ EPR determination.
基金supported by the Director,Office of Science,Office of Basic Energy Sciences,Division of Chemical,Geological and Biosciences of the U.S.Department of Energy under Contract No.DE-AC02-05CH11231
文摘Water oxidation, as a mandatory reaction of solar fuels conversion systems, requires the use of light absorbers with electronic properties that are well matched with those of the multi-electron catalyst in order to achieve high efficiency. Molecular light absorbers offer flexibility in fine tuning of orbital energetics,and metal oxide nanoparticles have emerged as robust oxygen evolving catalysts. Hence, these material choices offer a promising approach for the development of photocatalytic systems for water oxidation.However, efficient charge transfer coupling of molecular light absorbers and metal oxide nanoparticle catalysts has proven a challenge. Recent new approaches toward the efficient coupling of these components based on synthetic design improvements combined with direct spectroscopic observation and kinetic evaluation of charge transfer processes are discussed.
文摘The effect of chemical composition of highly active supported Ziegler-Natta catalysts with controlled morphology on the MWD of PE has been studied.It was shown the variation of transition metal compound in the MgCl_2-supported catalyst affect of MWD of PE produced in broad range:Vanadium-magnesium catalyst(VMC)produce PE with broad and bimodal MWD(M_w/M_n=14-21).MWD of PE,produced over titanium-magnesium catalyst(TMC)is narrow or medium depending on Ti content in the catalyst(M_w/M_n=3.1-4.8).The oxidation ...
