CO2 Reduction on Single-Atom Ir Catalysts with Chemical Functionalization

Author(s):  
Zheng-Zhe Lin ◽  
Xi-Mei Li ◽  
Xin-Wei Chen ◽  
Xi Chen

As promising catalytic systems, single-atom catalysts (SACs) demonstrate improved catalytic performance for electrochemical reactions. However, the pinning of metal atoms on surfaces usually depends on the adsorption on defects. In...

Catalysts ◽  
2021 ◽  
Vol 11 (12) ◽  
pp. 1470
Author(s):  
Nurul Asikin-Mijan ◽  
Haslinda Mohd Sidek ◽  
Abdulkareem G. AlSultan ◽  
Nurul Ahtirah Azman ◽  
Nur Athirah Adzahar ◽  
...  

Biofuels have been derived from various feedstocks by using thermochemical or biochemical procedures. In order to synthesise liquid and gas biofuel efficiently, single-atom catalysts (SACs) and single-atom alloys (SAAs) have been used in the reaction to promote it. SACs are made up of single metal atoms that are anchored or confined to a suitable support to keep them stable, while SAAs are materials generated by bi- and multi-metallic complexes, where one of these metals is atomically distributed in such a material. The structure of SACs and SAAs influences their catalytic performance. The challenge to practically using SACs in biofuel production is to design SACs and SAAs that are stable and able to operate efficiently during reaction. Hence, the present study reviews the system and configuration of SACs and SAAs, stabilisation strategies such as mutual metal support interaction and geometric coordination, and the synthesis strategies. This paper aims to provide useful and informative knowledge about the current synthesis strategies of SACs and SAAs for future development in the field of biofuel production.


2021 ◽  
Author(s):  
Youzhi Li ◽  
Bo Wei ◽  
Zhongjian Li ◽  
Lei Fan ◽  
Qike Jiang ◽  
...  

Abstract Although single-atom catalysts (SACs) have been widely employed in the CO2 reduction reaction (CO2RR), the understanding regarding the effect of morphological attributes on catalytic performance are still lacking, which prevents the rational design of high-performance catalysts for electrochemical CO2RR. Here, we developed a novel catalyst with axial Co-N5 sites embedded on controllable mesoporous carbon nanosphere with different graded pore structures. Benefiting from the precise control of porosity, the influence of morphological attributes on catalytic performance was well revealed. In situ characterization combined with density functional theory (DFT) calculations revealed that axial N-coordination induced local d-p orbitals coupling enhancement of Co with oxides and the optimal pore size of 27 nm promoted the interfacial bonding characteristics, which facilitate both the COOH* generation and CO desorption. Consequently, A superior selectivity of nearly 100% at -0.8 V vs. RHE and commercially relevant current densities of >150 mA cm−2 could be achieved, and a strikingly high turnover frequency of 1.136*104 h−1 at -1.0 V has been obtained, superior to the most of Co-based catalysts.


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Lin Ju ◽  
Xin Tan ◽  
Xin Mao ◽  
Yuantong Gu ◽  
Sean Smith ◽  
...  

AbstractEfficient and selective CO2 electroreduction into chemical fuels promises to alleviate environmental pollution and energy crisis, but it relies on catalysts with controllable product selectivity and reaction path. Here, by means of first-principles calculations, we identify six ferroelectric catalysts comprising transition-metal atoms anchored on In2Se3 monolayer, whose catalytic performance can be controlled by ferroelectric switching based on adjusted d-band center and occupation of supported metal atoms. The polarization dependent activation allows effective control of the limiting potential of CO2 reduction on TM@In2Se3 (TM = Ni, Pd, Rh, Nb, and Re) as well as the reaction paths and final products on Nb@In2Se3 and Re@In2Se3. Interestingly, the ferroelectric switching can even reactivate the stuck catalytic CO2 reduction on Zr@In2Se3. The fairly low limiting potential and the unique ferroelectric controllable CO2 catalytic performance on atomically dispersed transition-metals on In2Se3 clearly distinguish them from traditional single atom catalysts, and open an avenue toward improving catalytic activity and selectivity for efficient and controllable electrochemical CO2 reduction reaction.


2021 ◽  
Author(s):  
Hai-Long Jiang ◽  
Yan Zhang ◽  
Long Jiao ◽  
Weijie Yang ◽  
Chenfan Xie
Keyword(s):  

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Xiaowen Chen ◽  
Mi Peng ◽  
Xiangbin Cai ◽  
Yunlei Chen ◽  
Zhimin Jia ◽  
...  

AbstractMetal nanoparticle (NP), cluster and isolated metal atom (or single atom, SA) exhibit different catalytic performance in heterogeneous catalysis originating from their distinct nanostructures. To maximize atom efficiency and boost activity for catalysis, the construction of structure–performance relationship provides an effective way at the atomic level. Here, we successfully fabricate fully exposed Pt3 clusters on the defective nanodiamond@graphene (ND@G) by the assistance of atomically dispersed Sn promoters, and correlated the n-butane direct dehydrogenation (DDH) activity with the average coordination number (CN) of Pt-Pt bond in Pt NP, Pt3 cluster and Pt SA for fundamentally understanding structure (especially the sub-nano structure) effects on n-butane DDH reaction at the atomic level. The as-prepared fully exposed Pt3 cluster catalyst shows higher conversion (35.4%) and remarkable alkene selectivity (99.0%) for n-butane direct DDH reaction at 450 °C, compared to typical Pt NP and Pt SA catalysts supported on ND@G. Density functional theory calculation (DFT) reveal that the fully exposed Pt3 clusters possess favorable dehydrogenation activation barrier of n-butane and reasonable desorption barrier of butene in the DDH reaction.


Author(s):  
Simran Kumari ◽  
Philippe Sautet

Supported single-atom and small cluster catalysts have become highly popular in heterogeneous catalysis. These catalysts can maximize the metal atom utilization while still showcasing superior catalytic performance. One of the...


2022 ◽  
Vol 300 ◽  
pp. 120695 ◽  
Author(s):  
Minzhi Ma ◽  
Zeai Huang ◽  
Dmitry E. Doronkin ◽  
Wenjun Fa ◽  
Zhiqiang Rao ◽  
...  

2021 ◽  
Vol 23 (14) ◽  
pp. 8784-8791
Author(s):  
Qingling Meng ◽  
Ling Zhang ◽  
Jinge Wu ◽  
Shuwei Zhai ◽  
Xiamin Hao ◽  
...  

Theoretical screening of transition metal atoms anchored on monolayer C9N4 as highly stable, catalytically active and selective single-atom catalysts for nitrogen fixation.


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