Spatially Resolved and Quantitatively Revealed Charge Transfer between Single Atoms and Catalyst Supports

2021 ◽  
Author(s):  
Bin Di ◽  
Zhantao Peng ◽  
Zhongyi Wu ◽  
Xiong Zhou ◽  
Kai Wu
Keyword(s):  
Charge Transfer ◽  
Charge State ◽  
Catalytic Performance ◽  
Single Atom ◽  
Catalyst Supports ◽  
Single Atoms ◽  
Spatially Resolved

The charge state of supported single atoms is one of the most significant aspects determining the catalytic performance of single atom catalysts (SACs) which have drawn tremendous attention in recent...

scholarly journals Unraveling the coordination structure-performance relationship in Pt1/Fe2O3 single-atom catalyst

2019 ◽  
Vol 10 (1) ◽  
Author(s):  
Yujing Ren ◽  
Yan Tang ◽  
Leilei Zhang ◽  
Xiaoyan Liu ◽  
Lin Li ◽  
...  
Keyword(s):  
Coordination Chemistry ◽  
Homogeneous Catalysis ◽  
Catalytic Performance ◽  
Inert Atmosphere ◽  
Single Atom ◽  
Unique Role ◽  
Local Coordination ◽  
Single Atoms ◽  
Heterogeneous And Homogeneous Catalysis

Abstract Heterogeneous single-atom catalyst (SAC) opens a unique entry to establishing structure–performance relationship at the molecular level similar to that in homogeneous catalysis. The challenge lies in manipulating the coordination chemistry of single atoms without changing single-atom dispersion. Here, we develop an efficient synthetic method for SACs by using ethanediamine to chelate Pt cations and then removing the ethanediamine by a rapid thermal treatment (RTT) in inert atmosphere. The coordination chemistry of Pt single atoms on a Fe2O3 support is finely tuned by merely adjusting the RTT temperature. With the decrease in Pt-O coordination number, the oxidation state of Pt decreases, and consequently the hydrogenation activity increases to a record level without loss of chemoselectivity. The tunability of the local coordination chemistry, oxidation states of the metal, and the catalytic performance of single atoms reveals the unique role of SACs as a bridge between heterogeneous and homogeneous catalysis.

Highly Efficient Catalytic Properties of Sc and Fe Single Atoms Stabilized on Honeycomb Borophene/Al(111) heterostructure via a Dual Charge transfer effect

Nanoscale ◽  
2021 ◽  
Author(s):  
Mengru Ren ◽  
Lili Zhang ◽  
Yan Di Zhu ◽  
Jin Lei Shi ◽  
Xing Ju Zhao ◽  
...  
Keyword(s):  
Charge Transfer ◽  
Heterogeneous Catalysis ◽  
Catalytic Properties ◽  
Transfer Effect ◽  
Single Atom ◽  
Single Atoms ◽  
Highly Efficient ◽  
Theoretical Design ◽  
Metal Atoms

Theoretical design and experimental fabrication of highly efficient single-atom catalysts (SACs) containing isolated metal atoms monodispersed on appropriate substrates have surged to the forefront of heterogeneous catalysis in recent years....

scholarly journals Ligand-Metal Charge Transfer Induced via Adjustment of Textural Properties Controls the Performance of Single-Atom Catalysts During Photocatalytic Degradation

2021 ◽  
Author(s):  
Jiaxu Liu ◽  
Yajun Zou ◽  
Daniel Cruz ◽  
Aleksandr Savateev ◽  
Markus Antonietti ◽  
...  
Keyword(s):  
Charge Transfer ◽  
Heterogeneous Catalysts ◽  
Photophysical Properties ◽  
Organic Pollutant ◽  
Textural Properties ◽  
Single Atom ◽  
Single Atoms ◽  
Ligand Charge Transfer ◽  
Kinetic Investigations

Because of their peculiar nitrogen-rich structure, carbon nitrides are convenient polydentate ligands for designing single-atom-dispersed photocatalysts. However, the relation of catalysts textural properties with their photophysical properties and as a result activity in photocatalytic applications is rarely elaborated. Herein we report the preparation and characterization of a series of single-atom heterogeneous catalysts featuring highly-dispersed Ag and Cu species on mesoporous graphitic C<sub>3</sub>N<sub>4</sub>. We show that adjustment of materials textural properties and thereby metal single atoms coordination mode enables ligand-to-metal (LMCT) or ligand-to-metal-to-ligand charge transfer (LMLCT), a property tha was long speculated in single-atom catalysis but never observed. We employ the developed materials in the degradation of organic pollutant under irradiation with visible light. Kinetic investigations under flow conditions show that single atoms of Ag and Cu decrease the amount of toxic organic fragmentation products, while leading to a higher selectivity towards full calcination. The results correlate with the selected mode of charge transfer in the designed photocatalysts and provide a new understanding of the surface state of single-atom catalysts. The concepts can be exploited further to rationally design and optimize other single-atom materials.

scholarly journals Porous Materials Confining Single Atoms for Catalysis

2021 ◽  
Vol 9 ◽  
Author(s):  
Tao Zhu ◽  
Yiwei Han ◽  
Shuai Liu ◽  
Bo Yuan ◽  
Yatao Liu ◽  
...  
Keyword(s):  
Porous Material ◽  
Porous Materials ◽  
Shape Selectivity ◽  
Catalytic Performance ◽  
High Specific Surface Area ◽  
Single Atom ◽  
Research Progress ◽  
Porous Support ◽  
Support Materials ◽  
Single Atoms

In recent years, single-atom catalysts (SACs) have received extensive attention due to their unique structure and excellent performance. Currently, a variety of porous materials are used as confined single-atom catalysts, such as zeolites, metal-organic frameworks (MOFs), or carbon nitride (CN). The support plays a key role in determining the coordination structure of the catalytic metal center and its catalytic performance. For example, the strong interaction between the metal and the carrier induces the charge transfer between the metal and the carrier, and ultimately affects the catalytic behavior of the single-atom catalyst. Porous materials have unique chemical and physical properties including high specific surface area, adjustable acidity and shape selectivity (such as zeolites), and are rational support materials for confined single atoms, which arouse research interest in this field. This review surveys the latest research progress of confined single-atom catalysts for porous materials, which mainly include zeolites, CN and MOFs. The preparation methods, characterizations, application fields, and the interaction between metal atoms and porous support materials of porous material confined single-atom catalysts are discussed. And we prospect for the application prospects and challenges of porous material confined single-atom catalysts.

Synergetic role of charge transfer and strain engineering in improving the catalysis of Pd single-atom-thick motifs stabilized on a defect-free MoS2/Ag(Au)(111) heterostructure

2020 ◽  
Vol 8 (33) ◽  
pp. 17238-17247
Author(s):  
Zhixin Su ◽  
Rui Pang ◽  
Xiaoyan Ren ◽  
Shunfang Li
Keyword(s):  
Charge Transfer ◽  
Active Sites ◽  
Catalytic Performance ◽  
Strain Engineering ◽  
Single Atom

Single-atom-thick-PdN magic nanomotifs are demonstrated to be stabilized on defect-free MoS2 overlayer supported on Ag(111) via the synergetic role of charge transfer among the Pd active sites, leading to superior catalytic performance to SAC-Pd1.

scholarly journals Hydroxyl improving the activity, selectivity and stability of supported Ni single atoms for selective semi-hydrogenation

2021 ◽  
Author(s):  
Minzhen Jian ◽  
Jin-Xun Liu ◽  
Wei-Xue Li
Keyword(s):  
Catalytic Performance ◽  
Single Atom ◽  
Hydroxyl Group ◽  
Single Atoms ◽  
Supported Ni

Hydroxyl group can stabilize significantly Ni single atom by forming Ni1(OH)2 complexes on anatase TiO2(101), which displays high catalytic performance in acetylene semi-hydrogenation.

scholarly journals Ligand-Metal Charge Transfer Induced via Adjustment of Textural Properties Controls the Performance of Single-Atom Catalysts During Photocatalytic Degradation

2021 ◽  
Author(s):  
Jiaxu Liu ◽  
Yajun Zou ◽  
Daniel Cruz ◽  
Aleksandr Savateev ◽  
Markus Antonietti ◽  
...  
Keyword(s):  
Charge Transfer ◽  
Heterogeneous Catalysts ◽  
Photophysical Properties ◽  
Organic Pollutant ◽  
Textural Properties ◽  
Single Atom ◽  
Single Atoms ◽  
Ligand Charge Transfer ◽  
Kinetic Investigations

Because of their peculiar nitrogen-rich structure, carbon nitrides are convenient polydentate ligands for designing single-atom-dispersed photocatalysts. However, the relation of catalysts textural properties with their photophysical properties and as a result activity in photocatalytic applications is rarely elaborated. Herein we report the preparation and characterization of a series of single-atom heterogeneous catalysts featuring highly-dispersed Ag and Cu species on mesoporous graphitic C<sub>3</sub>N<sub>4</sub>. We show that adjustment of materials textural properties and thereby metal single atoms coordination mode enables ligand-to-metal (LMCT) or ligand-to-metal-to-ligand charge transfer (LMLCT), a property tha was long speculated in single-atom catalysis but never observed. We employ the developed materials in the degradation of organic pollutant under irradiation with visible light. Kinetic investigations under flow conditions show that single atoms of Ag and Cu decrease the amount of toxic organic fragmentation products, while leading to a higher selectivity towards full calcination. The results correlate with the selected mode of charge transfer in the designed photocatalysts and provide a new understanding of the surface state of single-atom catalysts. The concepts can be exploited further to rationally design and optimize other single-atom materials.

scholarly journals Reversing the charge transfer between platinum and sulfur-doped carbon support for electrocatalytic hydrogen evolution

2019 ◽  
Vol 10 (1) ◽  
Author(s):  
Qiang-Qiang Yan ◽  
Dao-Xiong Wu ◽  
Sheng-Qi Chu ◽  
Zhi-Qin Chen ◽  
Yue Lin ◽  
...  
Keyword(s):  
Charge Transfer ◽  
Hydrogen Evolution ◽  
Carbon Support ◽  
Catalytic Performance ◽  
High Mass ◽  
Carbon Supports ◽  
Pt Nanoclusters ◽  
Size Dependent ◽  
Single Atoms ◽  
Metal Support Interaction

Abstract Metal–support interaction is of great significance for catalysis as it can induce charge transfer between metal and support, tame electronic structure of supported metals, impact adsorption energy of reaction intermediates, and eventually change the catalytic performance. Here, we report the metal size-dependent charge transfer reversal, that is, electrons transfer from platinum single atoms to sulfur-doped carbons and the carbon supports conversely donate electrons to Pt when their size is expanded to ~1.5 nm cluster. The electron-enriched Pt nanoclusters are far more active than electron-deficient Pt single atoms for catalyzing hydrogen evolution reaction, exhibiting only 11 mV overpotential at 10 mA cm−2 and a high mass activity of 26.1 A mg−1 at 20 mV, which is 38 times greater than that of commercial Pt/C. Our work manifests that the manipulation of metal size-dependent charge transfer between metal and support opens new avenues for developing high-active catalysts.

Theoretical study of the electrochemical reduction of CO2 on cerium dioxide supported palladium single atoms and nanoparticles

2021 ◽  
Author(s):  
Yan nv Guo ◽  
haiyan zhu ◽  
He Zhao ◽  
Qinfu Zhao ◽  
Caihua Zhou ◽  
...  
Keyword(s):  
Electrochemical Reduction ◽  
Cerium Dioxide ◽  
Theoretical Study ◽  
Catalytic Performance ◽  
Single Atom ◽  
Pd Nanoparticle ◽  
Single Atoms ◽  
Nanoparticle Clusters ◽  
Supported Palladium ◽  
Reduction Of Co2

Pd/CeO2 catalysts show superior catalytic performance owing to their optimal cycling activity and stability. In this study, single-atom Pd and eight-atoms Pd nanoparticle clusters were supported on the surface of...

scholarly journals Ligand-Metal Charge Transfer Induced via Adjustment of Textural Properties Controls the Performance of Single-Atom Catalysts During Photocatalytic Degradation

2021 ◽  
Author(s):  
Jiaxu Liu ◽  
Yajun Zou ◽  
Daniel Cruz ◽  
Aleksandr Savateev ◽  
Markus Antonietti ◽  
...  
Keyword(s):  
Charge Transfer ◽  
Heterogeneous Catalysts ◽  
Photophysical Properties ◽  
Organic Pollutant ◽  
Textural Properties ◽  
Single Atom ◽  
Single Atoms ◽  
Ligand Charge Transfer ◽  
Kinetic Investigations

Because of their peculiar nitrogen-rich structure, carbon nitrides are convenient polydentate ligands for designing single-atom-dispersed photocatalysts. However, the relation of catalysts textural properties with their photophysical properties and as a result activity in photocatalytic applications is rarely elaborated. Herein we report the preparation and characterization of a series of single-atom heterogeneous catalysts featuring highly-dispersed Ag and Cu species on mesoporous graphitic C<sub>3</sub>N<sub>4</sub>. We show that adjustment of materials textural properties and thereby metal single atoms coordination mode enables ligand-to-metal (LMCT) or ligand-to-metal-to-ligand charge transfer (LMLCT), a property tha was long speculated in single-atom catalysis but never observed. We employ the developed materials in the degradation of organic pollutant under irradiation with visible light. Kinetic investigations under flow conditions show that single atoms of Ag and Cu decrease the amount of toxic organic fragmentation products, while leading to a higher selectivity towards full calcination. The results correlate with the selected mode of charge transfer in the designed photocatalysts and provide a new understanding of the surface state of single-atom catalysts. The concepts can be exploited further to rationally design and optimize other single-atom materials.

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