Electrostatic charge transfer for boosting the photocatalytic CO2 reduction on metal centers of 2D MOF/rGO heterostructure

2020 ◽  
Vol 262 ◽  
pp. 118144 ◽  
Author(s):  
Qiaoqiao Mu ◽  
Wei Zhu ◽  
Xian Li ◽  
Chufeng Zhang ◽  
Yanhui Su ◽  
...  
2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Mingzi Sun ◽  
Qiuyang Lu ◽  
Zhong Lin Wang ◽  
Bolong Huang

AbstractThe charge transfer phenomenon of contact electrification even exists in the liquid–solid interface by a tiny droplet on the solid surface. In this work, we have investigated the contact electrification mechanism at the liquid–solid interface from the electronic structures at the atomic level. The electronic structures display stronger modulations by the outmost shell charge transfer via surface electrostatic charge perturbation than the inter-bonding-orbital charge transfer at the liquid–solid interface, supporting more factors being involved in charge transfer via contact electrification. Meanwhile, we introduce the electrochemical cell model to quantify the charge transfer based on the pinning factor to linearly correlate the charge transfer and the electronic structures. The pinning factor exhibits a more direct visualization of the charge transfer at the liquid–solid interface. This work supplies critical guidance for describing, quantifying, and modulating the contact electrification induced charge transfer systems in triboelectric nanogenerators in future works.


Author(s):  
Zhenxin Lou ◽  
Wenjing Li ◽  
Haiyang Yuan ◽  
Yu Hou ◽  
Huagui Yang ◽  
...  

Metal single-atom catalysts (SACs) on nitrogen-doped carbons exhibit an attractive prospect in catalysis. However, how to quickly collocate various metal centers with diversified N-coordination topologic structures to maximize the catalytic...


2021 ◽  
Author(s):  
Qinying Pan ◽  
Mohamed Abdellah ◽  
Yuehan Cao ◽  
Yang Liu ◽  
Weihua Lin ◽  
...  

Abstract Rhenium(I)-carbonyl-diimine complexes are promising photocatalysts for CO2 reduction. Covalent organic frameworks (COFs) can be perfect sensitizers to enhance the reduction activities. Here we investigated the excited state dynamics of COF (TpBpy) with 2,2'-bipyridine incorporating Re(CO)5Cl (Re-TpBpy) to rationalize the underlying mechanism. The time-dependent DFT calculation first clarified excited state structure of the hybrid catalyst. The studies from transient visible and infrared spectroscopies revealed the excitation energy-dependent photo-induced charge transfer pathways in Re-TpBpy. Under low energy excitation, the electrons at the LUMO level are quickly injected from Bpy into ReI center (1–2 ps) followed by backward recombination (13 ps). Under high energy excitation, the hot-electrons are first injected into the higher unoccupied level of ReI center (1–2 ps) and then slowly relax back to the HOMO in COF (24 ps). There also remains long-lived free electrons in the COF moiety. This explained the excitation energy-dependent CO2 reduction performance in our system.


2020 ◽  
Vol 44 (39) ◽  
pp. 16795-16809 ◽  
Author(s):  
Zambaga Otgonbayar ◽  
Kwang Youn Cho ◽  
Won-Chun Oh

Effective charge transfer is a key factor in enhancing the catalytic activity of photocatalytic nanocomposite materials.


ACS Nano ◽  
2020 ◽  
Vol 14 (11) ◽  
pp. 15841-15852
Author(s):  
Peng Chen ◽  
Ben Lei ◽  
Xing’an Dong ◽  
Hong Wang ◽  
Jianping Sheng ◽  
...  

Langmuir ◽  
2012 ◽  
Vol 28 (32) ◽  
pp. 11656-11661 ◽  
Author(s):  
Do Jin Im ◽  
Myung Mo Ahn ◽  
Byeong Sun Yoo ◽  
Dustin Moon ◽  
Dong Woog Lee ◽  
...  

2021 ◽  
Vol 9 ◽  
Author(s):  
Dongsheng Li ◽  
Bichen Zhu ◽  
Zhongti Sun ◽  
Qinqin Liu ◽  
Lele Wang ◽  
...  

One of the basic challenges of CO2 photoreduction is to develop efficient photocatalysts, and the construction of heterostructure photocatalysts with intimate interfaces is an effective strategy to enhance interfacial charge transfer for realizing high photocatalytic activity. Herein, a novel UiO-66/Bi4O5Br2 heterostructure photocatalyst was constructed by depositing UiO-66 nanoparticles with octahedral morphology over the Bi4O5Br2 nanoflowers assembled from the Bi4O5Br2 nanosheets via an electrostatic self-assembly method. A tight contact interface and a built-in electric field were formed between the UiO-66 and the Bi4O5Br2, which was conducive to the photo-electrons transfer from the Bi4O5Br2 to the UiO-66 and the formation of a type-II heterojunction with highly efficient charge separation. As a result, the UiO-66/Bi4O5Br2 exhibited improved photocatalytic CO2 reduction performance with a CO generation rate of 8.35 μmol h−1 g−1 without using any sacrificial agents or noble co-catalysts. This work illustrates an applicable tactic to develop potent photocatalysts for clean energy conversion.


Author(s):  
Michele Melchionna ◽  
Paolo Fornasiero ◽  
Maurizio Prato ◽  
Marcella Bonchio

CO2RR is enhanced by the unique role of carbon nanostructures cooperating with metal and metal-oxide active phases to leverage charge transfer, reagent diffusion and structural stability, regulating a successful asset of interfacial interactions.


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