Research progress on metal-organic framework compounds (MOFs) in electrocatalysis.

Metal-organic frameworks (MOFs) have favorable characteristics such as large specific surface area, high porosity, structural diversity, and pore surface modification, giving them great potential for development and attractive prospects in the research area of modern materials electrocatalysis. However, unsatisfactory catalytic activity and poor electronic conductivity are the main challenges facing MOFs. This review focuses on MOF-based materials used in electrocatalysis, based on the types of catalytic reactions that have used MOF-based materials in recent years along with their applications, and also looks at some new electrocatalytic materials and their future development prospects.

Recent advances in catalytic oxidation of VOCs by two-dimensional ultra-thin nanomaterials.

Catalytic oxidation, an end-of-pipe treatment technology for effectively purifying volatile organic compounds (VOCs), has received widespread attention. The crux of catalytic oxidation lies in the development of efficient catalysts, with their optimization necessitating a comprehensive analysis of the catalytic reaction mechanism. Two-dimensional (2D) ultra-thin nanomaterials offer significant advantages in exploring the catalytic oxidation mechanism of VOCs due to their unique structure and properties. This review classifies strategies for regulating catalytic properties and typical applications of 2D materials in VOCs catalytic oxidation, in addition to their characteristics and typical characterization techniques. Furthermore, the possible reaction mechanism of 2D Co-based and Mn-based oxides in the catalytic oxidation of VOCs is analyzed, with a special focus on the synergistic effect between oxygen and metal vacancies. The objective of this review is to provide valuable references for scholars in the field.

δ-MnO2 decorated layered double oxides in-situ grown on nickel foam towards electrothermal catalysis of n-heptane.

Energy-saving and efficient monolithic catalysts are hotspots of catalytic purification of industrial gaseous pollutants. Here, we have developed an electrothermal catalytic mode, in which the ignition temperature required for the reaction is provided by Joule heat generated when the current flows through the catalyst. In this paper, Mn/NiAl/NF, Mn/NiFe/NF and Mn/NF metal-based monolithic catalysts were prepared using nickel foam (NF) as the carrier for thermal and electrothermal catalysis of n-heptane. The results indicated that Mn-based monolithic catalysts exhibit high activity in thermal and electrothermal catalysis. Mn/NiFe/NF achieve conversion of n-heptane more than 99% in electrothermal catalysis under a direct-current (DC) power of 6 W, and energy-saving is 54% compared with thermal catalysis. In addition, the results indicated that the introduction of NiAl (or NiFe) greatly enhanced the catalytic activity of Mn/NF, which attributed to the higher specific surface area, Mn3+/Mn4+, Ni3+/Ni2+, adsorbed oxygen species (Oads)/lattice oxygen species (Olatt), redox performance of the catalyst. Electrothermal catalytic activity was significantly higher than thermal catalytic activity before complete conversion, which may be related to electronic effects. Besides, Mn/NiFe/NF has good cyclic and long-term stability in electrothermal catalysis. This paper provided a theoretical basis for applying electrothermal catalysis in the field of VOCs elimination.

Stainless steel catalyst for air pollution control: structure, properties, and activity.

With the awakening of environmental awareness, the importance of air quality to human health and the proper functioning of social mechanisms is becoming increasingly prominent. The low cost and high efficiency of catalytic technique makes it a natural choice for achieving deep air purification. Stainless steel alloys have demonstrated their full potential for application in a variety of catalytic fields. The diversity of 3D networks or fibrous structures increases the turbulence within the heterogeneous catalysis, balance the temperature distribution in the reaction bed and, in combination with a highly thermally conductive skeleton, avoid agglomeration and deactivation of the active components; corrosion resistance and thermal stability are adapted to highly endothermic/exothermic or corrosive reaction environments; oxide layers formed by bulk transition metals activated by thermal treatment or etching can significantly alter the physico-chemical properties between the substrate and active species, further improving the stability of stainless steel catalysts; suitable electronic conductivity can be applied to the electrothermal catalysis, which is expected to provide guidance for the reduction of intermittent emission exhausts and the storage of renewable energy. The current applications of stainless steel as catalyst or support in the air purification have covered soot particle capture and combustion, catalytic oxidation of VOCs, SCR, and air sterilization. This paper summarizes several preparation methods and presents the relationships between the preparation process and the activity, and reviews its application and the current status of research in atmospheric environmental management, proposing the advantages and challenges of the stainless steel-based catalysts.

Air pollutant emission and reduction potentials from the sintering process of the iron and steel industry in China in 2017.

The iron and steel industry (ISI) is one of the most energy-intensive industries in China, which makes a substantial contribution to the emissions of air pollutants. Among the various manufacturing processes, sintering is the major emitting process, which shares over half of the emissions of sulfur dioxide (SO2), nitrogen oxide (NOx) and particulate matter (PM) for the entire industry. In this study we made a comprehensive evaluation of the air pollutant emissions from the sintering process of China's ISI in 2017 based on the Continuous Emission Monitoring System (CEMS) database and estimated the future reduction potentials. We found that there was a general decreasing trend of emission concentrations in the sintering flue gas in response to the strengthened emission control policies, but the mild increase of the oxygen content in the second half of the year flattened the decreasing trend, indicating the necessity for simultaneous control of the oxygen content in the flue gas. Despite the relative high standard-reaching rates of 90% to the emission concentration limits in GB 28662-2012, the standard-reaching rates to the ultra-low emission standards were only 12%, 40% and 27% for NOx, SO2 and PM respectively, with the lowest value mostly occurred in the western provinces. In 2017, the NOx, SO2 and PM emissions from the sintering process were 378.6 kt, 169.0 kt and 51.9 kt, respectively. If the ultra-low emission standards were met, the corresponding NOx, SO2 and PM emissions would decrease by 69.9%, 52.9%, and 56.4% respectively, illustrating large emission reducing potentials by achieving the ultra-low emission standards.

Trends in air pollutant emissions from the sintering process of the iron and steel industry in the Fenwei Plain and surrounding regions in China, 2014-2017.

China is the largest iron and steel producer and consumer in the world. The iron and steel manufacture, especially the sintering process, is energy-intensive, and contributes substantially to air pollutant emissions in China. Compared with other regions, the Fenwei Plain, a coal base, has a heavy industry concentration, and high pollutant emission total amount. In addition, urban air pollution has rebounded, and the pollutants concentrations in many cities have increased rather than decreased. In this study, we investigated the inter-annual trends of particulate matter (PM), sulfur dioxide (SO2) and nitrogen oxide (NOx) from the sintering process of iron and steel industry (ISI) in the Fenwei Plain and the surrounding regions in China from 2014 to 2017 based on the Continuous Emission Monitoring System (CEMS). We found that the oxygen content of the flue gas is the key to judge whether the sintering flue gas air pollutant emission concentration can meet the standard. Therefore, we adopted the converted concentration by the reference oxygen content in the final analysis. Overall, the SO2 and PM emission concentrations exhibit a downward trend from 2014 to 2017, in response to the strengthening of the emission control policies and standards in the ISI, whereas the NOx emission concentration did not change significantly during the same period The emission factors (EFs) of PM, NOx and SO2 obtained in this study are lower than previous estimates. In 2017, the SO2 and PM emissions were 27% and 32% lower than the levels in 2014.While NOx was 22% higher than the level in 2014. Our study confirmed the effectiveness of current emission control policies and standards in the iron and steel sector. However, the levels of NOx emissions were still high until 2017, illustrating the urgent need for more advanced emission control technologies to further reduce NOx emissions from the sintering flue gas in China.

Evolution mechanism of transition metal in NH3-SCR reaction over Mn-based bimetallic oxide catalysts: Structure-activity relationships.

The unexpected phenomenon in which different transition metals (Co, Ni and Cu) presented significant variation of participation levels as the auxiliaries in Mn-based bimetallic oxide catalysts were reported here. It is found that the Co element more easily to form Mn enriched surface bimetallic oxides with Mn than Ni and Cu, resulting in Co-MnOx exhibited the best deNOx activity and SO2 tolerance, followed by Ni-MnOx and Cu-MnOx. The role of different transition metal and structure-activity relationships were systematically investigated by advanced techniques including Synchrotron XAFS and in situ DRIFTs analysis. The excellent activity of Co-MnOx was related to its unique Mn-enriched surface (Co2+)tet(Mn3+ Co3+)octO4 structure with Mn cations occupying the octahedral sites, which is superior to the Ni-MnOx and Cu-MnOx with Mn-lean surface. In addition, the reaction energy barrier of Co-MnOx is weakened due to the lower electron cloud density around the Mn atom as compared to Ni-MnOx and Cu-MnOx. Moreover, Co-MnOx benefiting from the rapid electron migration between Mn and Co, more active bidentate/bridged nitrates could react with adsorbed NH3 in faster reaction rates following the L-H mechanism.

Isolated copper single sites for high-performance electroreduction of carbon monoxide to multicarbon products.

Electrochemical carbon monoxide reduction is a promising strategy for the production of value-added multicarbon compounds, albeit yielding diverse products with low selectivities and Faradaic efficiencies. Here, copper single atoms anchored to Ti3C2Tx MXene nanosheets are firstly demonstrated as effective and robust catalysts for electrochemical carbon monoxide reduction, achieving an ultrahigh selectivity of 98% for the formation of multicarbon products. Particularly, it exhibits a high Faradaic efficiency of 71% towards ethylene at -0.7 V versus the reversible hydrogen electrode, superior to the previously reported copper-based catalysts. Besides, it shows a stable activity during the 68-h electrolysis. Theoretical simulations reveal that atomically dispersed Cu-O3 sites favor the C-C coupling of carbon monoxide molecules to generate the key *CO-CHO species, and then induce the decreased free energy barrier of the potential-determining step, thus accounting for the high activity and selectivity of copper single atoms for carbon monoxide reduction.

Boosting carbonyl sulfide catalytic hydrolysis performance over N-doped Mg-Al oxide derived from MgAl-layered double hydroxide.

Carbonyl sulfide (COS), the organic sulfur generated in the chemical industry, has been receiving more attention due to its environmental and economic influence. In this study N-doped MgAl-LDO catalyst was successfully prepared and tested for the COS hydrolysis reaction at low temperature, it was observed that the N species can be formed both in surface and bulk. Moreover, the basicity property and the H2O adsorption-desorption property were remarkably improved due to the N-doping. Besides, the hydroxyl group can be formed more easily and more abundantly on N modified catalyst surface, which was beneficial to the COS adsorption and the remarkable improvement of catalytic performance. The catalytic hydrolysis performance can proceed for almost 1440 min without any deactivation at 70 °C. However, further increase of temperature was not beneficial to improve the catalytic performance due to the occurrence of H2S oxidation side reaction. Furthermore, it was revealed that the surface hydroxyl groups were responsible for the adsorption of COS and then the formed surface transitional species reacted with the H2O molecules. Hydrogen thiocarbonate and bicarbonate were the main reaction intermediate. The rate-determining step was IM6→IM7 i.e., a type transformation of bicarbonate.

Simultaneous removal of gaseous CO and elemental mercury over Cu-Co modified activated coke at low temperature.

Cu-Co multiple-oxides modified on HNO3-pretreated activated coke (ACN) were optimized for the simultaneous removal of gaseous CO and elemental mercury (Hg0) at low temperature (< 200 °C). It was found that 2%CuOx-10%CoOx/ACN catalyst calcined at 400°C resulted in the coexistence of complex oxides including CuO, Cu2O, Co3O4, Co2O3 and CoO phases, which might be good for the simultaneous catalytic oxidation of CO by Co-species and removal of Hg0 by Cu-species, benefiting from the synergistic catalysis during the electro-interaction between Co and Cu cations (CoO ⇌ Co3O4 and Cu2O ⇌ CuO). The catalysis removal of CO oxidation was obviously depended on the reaction temperature obtaining 94.7% at 200 °C, while no obvious promoting effect on the Hg0 removal (68.3%-78.7%). These materials were very substitute for the removal of CO and Hg° from the flue gas with the conditions of 8-20 vol.% O2 and flue-gas temperature below 200 °C. The removal of Hg° followed the combination processes of adsorption and catalytic oxidation reaction via Langmuir-Hinshelwood mechanism, while the catalysis of CO abided by the Mars-van Krevelen mechanism with lattice oxygen species.

Trifunctional Single-Atomic Ru Sites Enable Efficient Overall Water Splitting and Oxygen Reduction in Acidic Media.

Development of cost-effective, active trifunctional catalysts for acidic oxygen reduction (ORR) as well as hydrogen and oxygen evolution reactions (HER and OER, respectively) is highly desirable, albeit challenging. Herein, single-atomic Ru sites anchored onto Ti3 C2 Tx MXene nanosheets are first reported to serve as trifunctional electrocatalysts for simultaneously catalyzing acidic HER, OER, and ORR. A half-wave potential of 0.80 V for ORR and small overpotentials of 290 and 70 mV for OER and HER, respectively, at 10 mA cm-2 are achieved. Hence, a low cell voltage of 1.56 V is required for the acidic overall water splitting. The maximum power density of an H2 -O2 fuel cell using the as-prepared catalyst can reach as high as 941 mW cm-2 . Theoretical calculations reveal that isolated Ru-O2 sites can effectively optimize the adsorption of reactants/intermediates and lower the energy barriers for the potential-determining steps, thereby accelerating the HER, ORR, and OER kinetics.

Nitrogen doping and titanium vacancies synergistically promote CO2 fixation in seawater.

The electrocatalytic generation of useful chemicals from CO2, H2O, and sustainable energy resources offers a promising strategy for the carbon cycle. However, the current CO2 electrolysis system is mainly operated in artificial electrolytes (e.g. ionic liquids and inorganic salt solutions), of which the high cost and impractical working conditions hinder its large-scale development. In this case, seawater represents an attractive alternative due to its abundance and good conductivity. Herein, we show that N-doping and titanium vacancies (VTi) can be introduced in Ti3C2 MXene nanosheets via a facile NH3-etching pyrolysis approach. These nanosheets demonstrate impressive CO2 reduction reaction (CO2RR) performances in seawater with a remarkable 92% faradaic efficiency and a partial current density of -16.2 mA cm-2 for CO production, being close to those of noble metal electrodes. Mechanistic studies reveal that the existence of N dopants and VTi synergistically modulates the electronic structure of the active Ti site, on which the free energy barriers for the key *COOH formation and desorption of *CO are greatly reduced, thereby leading to a notable CO2RR improvement. This study provides an opportunity for developing an active and cost-effective CO2 electrolysis system by using seawater as the electrolyte.

Mn2NiO4 spinel catalyst for high-efficiency selective catalytic reduction of nitrogen oxides with good resistance to H2O and SO2 at low temperature.

Mn-Ni oxides with different compositions were prepared using standard co-precipitation (CP) and urea hydrolysis-precipitation (UH) methods and optimized for the selective catalytic reduction of nitrogen oxides (NOx) by NH3 at low temperature. Mn(2)Ni(1)Ox-CP and Mn(2)Ni(1)Ox-UH (with Mn:Ni molar ratio of 2:1) catalysts showed almost identical selective catalytic reduction (SCR) catalytic activity, with about 96% NOx conversion at 75°C and ~99% in the temperature range from 100 to 250°C. X-ray diffraction (XRD) results showed that Mn(2)Ni(1)Ox-CP and Mn(2)Ni(1)Ox-UH catalysts crystallized in the form of Mn2NiO4 and MnO2-Mn2NiO4 spinel, respectively. The latter gave relatively good selectivity to N2, which might be due to the presence of the MnO2 phase and high metal-O binding energy, resulting in low dehydrogenation ability. According to the results of various characterization methods, it was found that a high density of surface chemisorbed oxygen species and efficient electron transfer between Mn and Ni in the crystal structure of Mn2NiO4 spinel played important roles in the high-efficiency SCR activity of these catalysts. Mn(2)Ni(1)Ox catalysts presented good resistance to H2O or/and SO2 with stable activity, which benefited from the Mn2NiO4 spinel structure and Eley-Rideal mechanism, with only slight effects from SO2.

Facile fabrication of nanosheet-assembled MnCoOx hollow flower-like microspheres as highly effective catalysts for the low-temperature selective catalytic reduction of NOx by NH3.

A series of MnCoOx flower-like hollow microspheres with various molecular proportions of reactant were prepared through simple solvothermal method for the ammonia selective catalytic reduction (SCR) at low temperatures. The as-prepared samples have been applied by various characterization techniques to explore the formation process of the morphology and physicochemical properties. The Mn(1)Co(1)Ox presented the optimal intrinsic catalytic performance (95% NOx conversion at 75 °C), favorable thermal stability, and strong SO2 resistance. The excellent properties mainly related to its higher specific surface area and abundant active sites originated from hollow microsphere special structure consists of abundant nanosheets, robust redox properties beneficial for the strong interaction between the manganese and cobalt, larger number of acidic sites and stronger acid strength, etc., which collaboratively dominate its catalytic properties of NH3-SCR at low temperatures.

Fe-modified Ce-MnOx/ACFN catalysts for selective catalytic reduction of NOx by NH3 at low-middle temperature.

A series of MnOx/ACFN, Ce-MnOx/ACFN, and Fe-Ce-MnOx/ACFN catalysts on selective catalytic reduction (SCR) of NOx with NH3 at low-middle temperature had been successfully prepared through ultrasonic impregnation method, and the catalysts were characterized by SEM, XRD, BET, H2-TPR, NH3-TPD, XPS, and FT-IR spectroscopy, respectively. The results demonstrated that the 15 wt% Fe(1)-Ce(3)-MnOx(7)/ACFN catalyst achieved 90% NOx conversion (100~300 °C), good water resistance, and stability (175 °C). The excellent catalytic performance of the Fe(1)-Ce(3)-MnOx(7)/ACFN catalyst was mainly attributed to the interaction among Mn, Ce, and Fe. The doping of Fe promoted the dispersion of Ce and Mn and the formation of more Mn4+ and chemisorbed oxygen on the surface of a catalyst. This work laid a foundation for the successful application of active carbon fiber in the field of industrial denitrification, especially in the aspect of denitrification moving bed. Graphic abstract.

Study of reaction mechanism based on further promotion of low temperature degradation of toluene using nano-CeO2/Co3O4 under microwave radiation for cleaner production in spraying processing.

Cleaner production in spraying processing was presented by advanced low temperature oxidation technology using combined methods of microwave radiation and nano-composites. Activities of samples for oxidation of toluene were estimated and the result exhibited that application of microwave radiation and nano-materials greatly promoted activities of catalysts. Moreover, the doping of Ce further enhanced catalytic activities. Samples of 5% Ce-Co showed optimal activity with conversion rate of 70% and CO2 selection of 96% at 120 ℃ and 210 ℃, respectively. The lowest Ea (33.45 kJ/mol) was obtained calculating from kinetics process under microwave radiation using 5% Ce-Co indicating that the degradation of toluene might proceed more readily. Microwave absorption properties were first used tentatively to study the effect of "hot spots" induced by microwave radiation on catalytic oxidation of VOCs. Further, physicochemical properties of samples were also showed by XRD, SEM and XPS profiles to study oxidation activities of toluene. The maximum difference of toluene oxidation between no water and in water using 5% Ce-Co at 210 ℃ was only 3.06% manifesting that effects of moisture on activities were weak under microwave radiation. A possible degradation track using microwave heating was presented by the analysis of reaction byproducts using the GC-MS.

Mn-CeOx/MeOx(Ti, Al)/cordierite preparation with ultrasound-assisted for non-methane hydrocarbon removal from cooking oil fumes.

Cooking oil fumes (COFs) which contains a variety of volatile organic compounds (VOCs) is noxious not only to the environment but also to human health. Among COFs, the Non-methane Hydrocarbon (NMHC) removal rate is an index of the removal rate of COFs in the latest COFs purification standard (DB 11/1488-2018). Ultrasonic treatment can assist the synthesis of catalysts by creating "cavitation", which can improve the surface microtopography of catalysts. The research results in this paper revealed that the NMHC conversion of catalysts with ultrasonic treatment increased significantly. Besides, the samples that coated TiO2 had a higher conversion of NMHC than that coated Al2O3 because TiO2 has better oxidation performance than Al2O3. According to the XPS, SEM, EDS and BET data, because of the enhancement of interaction of the active components of catalysts caused by ultrasonic intervention, T-UU-CTAB exhibited the best catalytic performance, which attributed to the high levels of Mn4+/Mn3+, Ce4+/Ce3+ and Oads/Olatt, more developed pore structure owing to the smaller particle size, higher dispersion of active components, larger specific surface area and larger total pore volume produced by the ultrasonic treatment. Moreover, the conversion of NMHC over T-UU-CTAB is 93.6% at 400 °C.

Cordierite-supported metal oxide for non-methane hydrocarbon oxidation in cooking oil fumes.

Cooking emission is an important reason for the air quality deterioration in the metropolitan area in China. Transition metal oxide and different loading of manganese oxide supported on cordierite were prepared by incipient wetness impregnation method and were used for non-methane hydrocarbon (NMHC) oxidation in cooking oil fumes (COFs). The effects of different calcination temperature and different Mn content were also studied. The SEM photographs and CO2 temperature-programmed desorption revealed 5 wt% Mn/cordierite had the best pore structure and the largest number of the weak and moderate basic sites so it showed the best performance for NMHC oxidation. XRD analysis exhibited 5 wt% Mn/cordierite had the best dispersion of active phase and the active phase was MnO2 when the calcination temperature was 400℃ which were good for the catalytic oxidation of NMHC.

Atomically Dispersed Molybdenum Catalysts for Efficient Ambient Nitrogen Fixation.

NH3 synthesis by the electrocatalytic N2 reduction reaction (NRR) under ambient conditions is an appealing alternative to the currently employed industrial method-the Haber-Bosch process-that requires high temperature and pressure. We report single Mo atoms anchored to nitrogen-doped porous carbon as a cost-effective catalyst for the NRR. Benefiting from the optimally high density of active sites and hierarchically porous carbon frameworks, this catalyst achieves a high NH3 yield rate (34.0±3.6 µg NH 3 h-1 mgcat. -1 ) and a high Faradaic efficiency (14.6±1.6 %) in 0.1 m KOH at room temperature. These values are considerably higher compared to previously reported non-precious-metal electrocatalysts. Moreover, this catalyst displays no obvious current drop during a 50 000 s NRR, and high activity and durability are achieved in 0.1 m HCl. The findings provide a promising lead for the design of efficient and robust single-atom non-precious-metal catalysts for the electrocatalytic NRR.

Self-powered H2 production with bifunctional hydrazine as sole consumable.

Splitting hydrazine into H2 and N2 by electro-catalyzing hydrogen evolution and hydrazine oxidation reactions is promising for replacing fossil energy with H2. However, current hydrazine splitting is achieved using external powers to drive the two reactions, which is inapplicable to outdoor use. Here, Fe-doped CoS2 nanosheets are developed as a bifunctional electrocatalyst for the two reactions, by which direct hydrazine fuel cells and overall-hydrazine-splitting units are realized and integrated to form a self-powered H2 production system. Without external powers, this system employs hydrazine bifunctionally as the fuel of direct hydrazine fuel cell and the splitting target, namely a sole consumable, and exhibits an H2 evolution rate of 9.95 mmol h-1, a 98% Faradaic efficiency and a 20-h stability, all comparable to the best reported for self-powered water splitting. These performances are due to that Fe doping decreases the free-energy changes of H adsorption and adsorbed NH2NH2 dehydrogenation on CoS2.