scholarly journals Tuning the Covering on Gold Surfaces by Grafting Amino-Aryl Films Functionalized with Fe(II) Phthalocyanine: Performance on the Electrocatalysis of Oxygen Reduction

Molecules ◽  
2021 ◽  
Vol 26 (6) ◽  
pp. 1631
Author(s):  
Camila F. Olguín ◽  
Nicolás Agurto ◽  
Carlos P. Silva ◽  
Carolina P. Candia ◽  
Mireya Santander-Nelli ◽  
...  

Current selective modification methods, coupled with functionalization through organic or inorganic molecules, are crucial for designing and constructing custom-made molecular materials that act as electroactive interfaces. A versatile method for derivatizing surfaces is through an aryl diazonium salt reduction reaction (DSRR). A prominent feature of this strategy is that it can be carried out on various materials. Using the DSRR, we modified gold surface electrodes with 4-aminebenzene from 4-nitrobenzenediazonium tetrafluoroborate (NBTF), regulating the deposited mass of the aryl film to achieve covering control on the electrode surface. We got different degrees of covering: monolayer, intermediate, and multilayer. Afterwards, the ArNO2 end groups were electrochemically reduced to ArNH2 and functionalized with Fe(II)-Phthalocyanine to study the catalytic performance for the oxygen reduction reaction (ORR). The thickness of the electrode covering determines its response in front of ORR. Interestingly, the experimental results showed that an intermediate covering film presents a better electrocatalytic response for ORR, driving the reaction by a four-electron pathway.

Nanomaterials ◽  
2018 ◽  
Vol 8 (11) ◽  
pp. 955 ◽  
Author(s):  
Jing Liu ◽  
Jiao Yin ◽  
Bo Feng ◽  
Tao Xu ◽  
Fu Wang

The Pt particles within diameters of 1–3 nm known as Pt nanoclusters (NCs) are widely considered to be satisfactory oxygen reduction reaction (ORR) catalysts due to higher electrocatalytic performance and cost effectiveness. However, the utilization of such smaller Pt NCs is always limited by the synthesis strategies, stability and methanol tolerance of Pt. Herein, unprotected Pt NCs (~2.2 nm) dispersed on carbon nanotubes (CNTs) were prepared via a modified top-down approach using liquid Li as a solvent to break down the bulk Pt. Compared with the commercial Pt/C, the resultant Pt NCs/CNTs catalyst (Pt loading: 10 wt.%) exhibited more desirable ORR catalytic performance in 0.1 M HClO4. The specific activity (SA) and mass activity (MA) at 0.9 V for ORR over Pt NCs/CNTs were 2.5 and 3.2 times higher than those over the commercial Pt/C (Pt loading: 20 wt.%). Meanwhile, the Pt NCs/CNTs catalyst demonstrated more satisfactory stability and methanol tolerance. Compared with the obvious loss (~69%) of commercial Pt/C, only a slight current decrease (~10%) was observed for Pt NCs/CNTs after the chronoamperometric measurement for 2 × 104 s. Hence, the as-prepared Pt NCs/CNTs material displays great potential as a practical ORR catalyst.


ACS Catalysis ◽  
2013 ◽  
Vol 3 (6) ◽  
pp. 1263-1271 ◽  
Author(s):  
Yuanyuan Jiang ◽  
Yizhong Lu ◽  
Xiangyu Lv ◽  
Dongxue Han ◽  
Qixian Zhang ◽  
...  

2020 ◽  
Vol 12 (1) ◽  
Author(s):  
Yin Jia ◽  
Xuya Xiong ◽  
Danni Wang ◽  
Xinxuan Duan ◽  
Kai Sun ◽  
...  

AbstractImmobilizing metal atoms by multiple nitrogen atoms has triggered exceptional catalytic activity toward many critical electrochemical reactions due to their merits of highly unsaturated coordination and strong metal-substrate interaction. Herein, atomically dispersed Fe-NC material with precise sulfur modification to Fe periphery (termed as Fe-NSC) was synthesized, X-ray absorption near edge structure analysis confirmed the central Fe atom being stabilized in a specific configuration of Fe(N3)(N–C–S). By enabling precisely localized S doping, the electronic structure of Fe-N4 moiety could be mediated, leading to the beneficial adjustment of absorption/desorption properties of reactant/intermediate on Fe center. Density functional theory simulation suggested that more negative charge density would be localized over Fe-N4 moiety after S doping, allowing weakened binding capability to *OH intermediates and faster charge transfer from Fe center to O species. Electrochemical measurements revealed that the Fe-NSC sample exhibited significantly enhanced oxygen reduction reaction performance compared to the S-free Fe-NC material (termed as Fe-NC), showing an excellent onset potential of 1.09 V and half-wave potential of 0.92 V in 0.1 M KOH. Our work may enlighten relevant studies regarding to accessing improvement on the catalytic performance of atomically dispersed M-NC materials by managing precisely tuned local environments of M-Nx moiety.


2019 ◽  
Vol 7 (27) ◽  
pp. 16508-16515 ◽  
Author(s):  
Guanying Ye ◽  
Qian He ◽  
Suqin Liu ◽  
Kuangmin Zhao ◽  
Yuke Su ◽  
...  

Atomically dispersed iron doped-MOF-derived carbon with high iron loading and nitrogen content for the oxygen reduction reaction via a cage-confinement strategy shows excellent catalytic performance.


Nano Energy ◽  
2016 ◽  
Vol 20 ◽  
pp. 134-143 ◽  
Author(s):  
Li An ◽  
Huijun Yan ◽  
Xin Chen ◽  
Biao Li ◽  
Zhonghong Xia ◽  
...  

ChemCatChem ◽  
2015 ◽  
Vol 7 (18) ◽  
pp. 2937-2944 ◽  
Author(s):  
Shiping Wang ◽  
Minglei Zhu ◽  
Xiaobing Bao ◽  
Jing Wang ◽  
Chunhong Chen ◽  
...  

2016 ◽  
Vol 4 (22) ◽  
pp. 8803-8811 ◽  
Author(s):  
Tao Fu ◽  
Jun Fang ◽  
Chunsheng Wang ◽  
Jinbao Zhao

Novel hollow porous Ag–Pt bimetallic nanoparticles with better ORR catalytic performance than commercial Pt/C and Ag@Pt nanoparticles.


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