Superior performance of 3 D Co-Ni bimetallic oxides for catalytic degradation of organic dye: Investigation on the effect of catalyst morphology and catalytic mechanism

2016 ◽  
Vol 186 ◽  
pp. 193-203 ◽  
Author(s):  
Xueyan Liu ◽  
Dan Xu ◽  
Danfeng Zhang ◽  
Guozhen Zhang ◽  
Lei Zhang
2009 ◽  
Vol 92 (3-4) ◽  
pp. 333-340 ◽  
Author(s):  
Wei Li ◽  
Shun Zhao ◽  
Bin Qi ◽  
Yang Du ◽  
Xiaohong Wang ◽  
...  

2020 ◽  
Author(s):  
Jie Yang ◽  
Wenzhao Fu ◽  
Chaoqiu Chen ◽  
Wenyao Chen ◽  
Wugen Huang ◽  
...  

Abstract Rational synthesis of sub-nanocatalysts with controllable electronic and atomic structures remains a challenge to break the limits of traditional catalysts for superior performance. Here we report the atomic-level precise synthesis of Pt/graphene sub-nanocatalysts (from single atom, dimer, and to cluster) by atomic layer deposition, achieved by a novel high temperature pulsed ozone strategy to controllably pre-create abundant in-plane epoxy groups on graphene as anchoring sites. The specific in-plane epoxy structure endows the deposited Pt species with outstanding uniformity, controllability and stability. Their size-depended electronic and geometric effects have been observed for ammonia borane hydrolysis, revealing a volcano-type dependence of intrinsic activity on their sizes. Their active site structures have been identified based on extensive characterizations, dynamic compensation effect, kinetic isotope experiments and density function theory simulation. The Pt dimers show the highest catalytic activity and good durability than Pt single atoms and nanoparticles, ascribed to the unique C-Pt-Pt-O (C5Pt2O, metal-metal bond dimer) active site structure. Our work provides new insights into the precise tailoring and catalytic mechanism in sub-nanometer level.


2014 ◽  
Vol 139 ◽  
pp. 244-249 ◽  
Author(s):  
Tamanna Ishrat Farhana ◽  
M. Yousuf Ali Mollah ◽  
Md. Abu Bin Hasan Susan ◽  
Md. Mominul Islam

RSC Advances ◽  
2015 ◽  
Vol 5 (7) ◽  
pp. 5123-5130 ◽  
Author(s):  
Junying Tian ◽  
Peng Tian ◽  
Guiling Ning ◽  
Hongchang Pang ◽  
Qiang Song ◽  
...  

Hierarchical and porous MgAl2O4 spinel with excellent absorption performance has been synthesized via a facile hard template process.


2021 ◽  
Author(s):  
Dingguo Xia ◽  
Guang Feng ◽  
Fanghua Ning ◽  
Jin Song ◽  
Huaifang Shang ◽  
...  

Abstract The development of intrinsically effective and low-cost catalysts is critical for the large-scale commercial applications of electrocatalytic hydrogen production. Although various electrocatalysts have demonstrated high activities for hydrogen evolution reaction (HER), it remains a formidable challenge to develop an extremely efficient and durable catalyst for practical use, especially in acidic media. Here, we report quinary ultrasmall NiCoFePtRh high-entropy alloy (us-HEA) nanoparticles (NPs) with extremely superior performance for HER. The us-HEA NPs are well dispersed on the carbon supports, with an average diameter of 1.68 nm, which is the smallest size in the reported HEAs. The us-HEA/C achieves an ultrahigh mass activity of 28.3 A mg-1noble metals (much higher than that of other reported advanced catalysts) at -0.05 V (vs the reversible hydrogen electrode, RHE) for HER in 0.5 M H2SO4 solution, which is 40.4 and 74.5 times higher than those of the commercial Pt/C and Rh/C catalysts, respectively. Moreover, the us-HEA/C demonstrates the highest reported turnover frequency of 30.1 s−1 at 50 mV overpotential (41.8 times higher than that of the Pt/C catalyst) and excellent stability with no decay after 10,000 cycles. Both operando X-ray absorption spectroscopy and theoretical calculations reveal the true active sites and a synergistic effect among five elements, which endow us-HEA/C with significantly enhanced HER activity. This work not only provides a general and facile strategy for synthesizing us-HEA NPs, highlights HEAs as sufficiently advanced materials in energy electrocatalysis, but also acts as a guidance for elucidating the actual reaction process and catalytic mechanism of complex multi-element systems.


2019 ◽  
Vol 6 (5) ◽  
pp. 055801 ◽  
Author(s):  
A Rafiq ◽  
M Imran ◽  
M Ikram ◽  
M Naz ◽  
M Aqeel ◽  
...  

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