scholarly journals Layered Double Hydroxide (LDH) Based Photocatalysts: An Outstanding Strategy for Efficient Photocatalytic CO2 Conversion

Catalysts ◽  
2020 ◽  
Vol 10 (10) ◽  
pp. 1185 ◽  
Author(s):  
Abdul Razzaq ◽  
Shahzad Ali ◽  
Muhammad Asif ◽  
Su-Il In
Keyword(s):  
Low Cost ◽  
High Surface ◽  
High Surface Area ◽  
Co2 Concentration ◽  
Co2 Conversion ◽  
Critical Issues ◽  
Fuels And Chemicals ◽  
Double Hydroxide ◽  
Double Hydroxides ◽  
Photocatalytic Co2 Conversion

CO2 conversion to solar fuels/chemicals is an alluring approach for narrowing critical issues of global warming, environmental pollution, and climate change, caused by excess atmospheric CO2 concentration. Amongst various CO2 conversion strategies, photocatalytic CO2 conversion (PCC) is considered as a promising approach, which utilizes inexpensive sunlight and water with a photocatalyst material. Hence, development of an efficient and a stable photocatalyst is an essential activity for the respective scientific community to upscale the PCC research domain. Until today, metal oxides, such as TiO2, ZnO, etc., are categorized as standard photocatalysts because of their relative stability, abundant availability and low cost. However, their performance is tethered by limited light absorption and somewhat physical properties. Recently, layered double hydroxides (LDHs) have offered an exciting and efficient way for PCC due to their superb CO2 adsorption and moderate photocatalytic properties. The LDH based photocatalysts show marvelous physiochemical and electrical properties like high surface area, stability, and excellent conductivity. In the present review article, a summarized survey is portrayed regarding latest development for LDH based photocatalysts with a focus on synthesis strategies employing various photocatalyst materials, influencing parameters and possible mechanism involved in PCC to useful fuels and chemicals like CO, CH4, CH3OH, and H2.

Synthesis and characterisation of aqueous miscible organic-layered double hydroxides

2014 ◽  
Vol 2 (36) ◽  
pp. 15102-15110 ◽  
Author(s):  
Chunping Chen ◽  
Miaosen Yang ◽  
Qiang Wang ◽  
Jean-Charles Buffet ◽  
Dermot O'Hare
Keyword(s):  
Surface Area ◽  
Layered Double Hydroxide ◽  
Layered Double Hydroxides ◽  
High Surface ◽  
High Surface Area ◽  
New Family ◽  
Double Hydroxide ◽  
Double Hydroxides

We report the synthesis and characterisation of a new family of high surface area and dispersible layered double hydroxides entitled Aqueous Miscible Organic Layered Double Hydroxide (AMO-LDH).

scholarly journals Synthesis of catalysts with fine platinum particles supported by high-surface-area activated carbons and optimization of their catalytic activities for polymer electrolyte fuel cells

RSC Advances ◽  
2021 ◽  
Vol 11 (33) ◽  
pp. 20601-20611
Author(s):  
Md. Mijanur Rahman ◽  
Kenta Inaba ◽  
Garavdorj Batnyagt ◽  
Masato Saikawa ◽  
Yoshiki Kato ◽  
...  
Keyword(s):  
Fuel Cells ◽  
Polymer Electrolyte ◽  
High Performance ◽  
Activated Carbons ◽  
Low Cost ◽  
High Surface ◽  
High Surface Area ◽  
Polymer Electrolyte Fuel Cells ◽  
Supported Platinum ◽  
Platinum Particles

Herein, we demonstrated that carbon-supported platinum (Pt/C) is a low-cost and high-performance electrocatalyst for polymer electrolyte fuel cells (PEFCs).

scholarly journals Effects of Annealing Temperature on the Oxygen Evolution Reaction Activity of Copper–Cobalt Oxide Nanosheets

Nanomaterials ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 657
Author(s):  
Geul Han Kim ◽  
Yoo Sei Park ◽  
Juchan Yang ◽  
Myeong Je Jang ◽  
Jaehoon Jeong ◽  
...  
Keyword(s):  
High Activity ◽  
Cobalt Oxide ◽  
Oxygen Evolution ◽  
Oxygen Evolution Reaction ◽  
Low Cost ◽  
High Surface ◽  
High Surface Area ◽  
Cobalt Hydroxide ◽  
Ni Foam ◽  
Electron Conduction

Developing high performance, highly stable, and low-cost electrodes for the oxygen evolution reaction (OER) is challenging in water electrolysis technology. However, Ir- and Ru-based OER catalysts with high OER efficiency are difficult to commercialize as precious metal-based catalysts. Therefore, the study of OER catalysts, which are replaced by non-precious metals and have high activity and stability, are necessary. In this study, a copper–cobalt oxide nanosheet (CCO) electrode was synthesized by the electrodeposition of copper–cobalt hydroxide (CCOH) on Ni foam followed by annealing. The CCOH was annealed at various temperatures, and the structure changed to that of CCO at temperatures above 250 °C. In addition, it was observed that the nanosheets agglomerated when annealed at 300 °C. The CCO electrode annealed at 250 °C had a high surface area and efficient electron conduction pathways as a result of the direct growth on the Ni foam. Thus, the prepared CCO electrode exhibited enhanced OER activity (1.6 V at 261 mA/cm2) compared to those of CCOH (1.6 V at 144 mA/cm2), Co3O4 (1.6 V at 39 mA/cm2), and commercial IrO2 (1.6 V at 14 mA/cm2) electrodes. The optimized catalyst also showed high activity and stability under high pH conditions, demonstrating its potential as a low cost, highly efficient OER electrode material.

scholarly journals A new biocompatible ternary Layered Double Hydroxide Adsorbent for ultrafast removal of anionic organic dyes

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Garima Rathee ◽  
Amardeep Awasthi ◽  
Damini Sood ◽  
Ravi Tomar ◽  
Vartika Tomar ◽  
...  
Keyword(s):  
Waste Water ◽  
Methyl Orange ◽  
Surface Area ◽  
Layered Double Hydroxide ◽  
Removal Efficiency ◽  
Organic Dyes ◽  
High Surface ◽  
High Surface Area ◽  
Morphological Studies ◽  
Double Hydroxide

Abstract It would be of great significance to introduce a new biocompatible Layered Double Hydroxide (LDH) for the efficient remediation of wastewater. Herein, we designed a facile, biocompatible and environmental friendly layered double hydroxide (LDH) of NiFeTi for the very first time by the hydrothermal route. The materialization of NiFeTi LDH was confirmed by FTIR, XRD and Raman studies. BET results revealed the high surface area (106 m2/g) and the morphological studies (FESEM and TEM) portrayed the sheets-like structure of NiFeTi nanoparticles. The material so obtained was employed as an efficient adsorbent for the removal of organic dyes from synthetic waste water. The dye removal study showed >96% efficiency for the removal of methyl orange, congo red, methyl blue and orange G, which revealed the superiority of material for decontamination of waste water. The maximum removal (90%) of dyes was attained within 2 min of initiation of the adsorption process which supported the ultrafast removal efficiency. This ultrafast removal efficiency was attributed to high surface area and large concentration of -OH and CO32− groups present in NiFeTi LDH. In addition, the reusability was also performed up to three cycles with 96, 90 and 88% efficiency for methyl orange. Furthermore, the biocompatibility test on MHS cell lines were also carried which revealed the non-toxic nature of NiFeTi LDH at lower concentration (100% cell viability at 15.6 μg/ml). Overall, we offer a facile surfactant free method for the synthesis of NiFeTi LDH which is efficient for decontamination of anionic dyes from water and also non-toxic.

scholarly journals Bifunctional acid–base mesoporous silica@aqueous miscible organic-layered double hydroxides

RSC Advances ◽  
2019 ◽  
Vol 9 (7) ◽  
pp. 3749-3754 ◽  
Author(s):  
Hongri Suo ◽  
Haohong Duan ◽  
Chunping Chen ◽  
Jean-Charles Buffet ◽  
Dermot O'Hare
Keyword(s):  
Mesoporous Silica ◽  
Pore Size ◽  
Layered Double Hydroxides ◽  
High Surface ◽  
High Surface Area ◽  
Core Shell ◽  
Acid Base ◽  
Double Hydroxides ◽  
Hierarchical Morphology ◽  
Size And Structure

Core@shell materials which exhibit hierarchical morphology with ultra high surface area and controllable pore size and structure have been synthesised.

Morphology dependent adsorption of methylene blue on trititanate nanoplates and nanotubes prepared by the hydrothermal treatment of TiO2

2016 ◽  
Vol 75 (2) ◽  
pp. 350-357
Author(s):  
Graham Dawson ◽  
Wei Chen ◽  
Luhua Lu ◽  
Kai Dai
Keyword(s):  
Methylene Blue ◽  
Adsorption Capacity ◽  
Surface Area ◽  
Pore Volume ◽  
Hydrothermal Reaction ◽  
Low Cost ◽  
High Surface ◽  
High Surface Area ◽  
High Capacity ◽  
Adsorption Properties

The adsorption properties of two nanomorphologies of trititanate, nanotubes (TiNT) and plates (TiNP), prepared by the hydrothermal reaction of concentrated NaOH with different phases of TiO2, were examined. It was found that the capacity for both morphologies towards methylene blue (MB), an ideal pollutant, was extremely high, with the TiNP having a capacity of 130 mg/g, higher than the TiNT, whose capacity was 120 mg/g at 10 mg/L MB concentration. At capacity, the well-dispersed powders deposit on the floor of the reaction vessel. The two morphologies had very different structural and adsorption properties. TiNT with high surface area and pore volume exhibited exothermic monolayer adsorption of MB. TiNP with low surface area and pore volume yielded a higher adsorption capacity through endothermic multilayer adsorption governed by pore diffusion. TiNP exhibited a higher negative surface charge of −23 mV, compared to −12 mV for TiNT. The adsorption process appears to be an electrostatic interaction, with the cationic dye attracted more strongly to the nanoplates, resulting in a higher adsorption capacity and different adsorption modes. We believe this simple, low cost production of high capacity nanostructured adsorbent material has potential uses in wastewater treatment.

Highly active mixed-valent MnOxspheres constructed by nanocrystals as efficient catalysts for long-cycle Li–O2batteries

2016 ◽  
Vol 4 (43) ◽  
pp. 17129-17137 ◽  
Author(s):  
Sanpei Zhang ◽  
Zhaoyin Wen ◽  
Yang Lu ◽  
Xiangwei Wu ◽  
Jianhua Yang
Keyword(s):  
Surface Area ◽  
Low Cost ◽  
High Surface ◽  
High Surface Area ◽  
Long Cycle ◽  
Highly Active

We demonstrate a low-cost and facile strategy to synthesize mixed-valent MnOxspheres constructed from nanocrystals (~5 nm), containing MnII, MnIII, and MnIVspecies. Such highly active mixed-valent MnOxspheres with high surface area greatly improve the performance of Li–O2batteries.

Influence of nanoparticles on the polymer-conditioned dewatering of wastewater sludges

2013 ◽  
Vol 67 (9) ◽  
pp. 2117-2123
Author(s):  
N. J. Boyle ◽  
G. M. Evans
Keyword(s):  
Activated Sludge ◽  
Titanium Dioxide Nanoparticles ◽  
Low Cost ◽  
High Surface ◽  
High Surface Area ◽  
Wastewater Sludge ◽  
Small Scale ◽  
Sludge Dewatering ◽  
Solids Content ◽  
The Impact

The effect of using small-scale, high surface area, nanoparticles to supplement polymer-conditioned wastewater sludge dewatering was investigated. Aerobically digested sludge and waste activated sludge sourced from the Hunter Valley, NSW, Australia, were tested with titanium dioxide nanoparticles. The sludge samples were dosed with the nanoparticles in an attempt to adsorb a component of the charged biopolymer surfactants present naturally in sludge. The sludge was conditioned with a cationic polymer. The dewatering characteristics were assessed by measuring the specific resistance to filtration through a modified time-to-filter testing apparatus. The solids content of the dosed samples was determined by a mass balance and compared to the original solids content in the activated sludge. Test results indicated that nanoparticle addition modified the structure of the sludge and provided benefits in terms of the dewatering rate. The samples dosed with nanoparticles exhibited faster water removal, indicating a more permeable filter cake and hence more permeable sludge. A concentration of 2–4% nanoparticles was required to achieve a noticeable benefit. As a comparison, the sludge samples were also tested with a larger particle size, powdered activated carbon (PAC). It was found that the PAC did provide some minor benefits to sludge dewatering but was outperformed by the nanoparticles. The solids content of the final sludge was increased by a maximum of up to 0.6%. The impact of the order sequence of particles and polymer was also investigated. It was found that nanoparticles added before polymer addition provided the best dewatering performance. This outcome was consistent with current theories and previous research through the literature. An economic analysis was undertaken to confirm the viability of the technology for implementation at a full-scale plant. It was found that, currently, this technology is unlikely to be favourable unless the nanoparticles can be sourced for a low cost.

scholarly journals Green and facile synthesis of cerium doped Ni3Fe electrocatalyst for efficient oxygen evolution reaction

2020 ◽  
Vol 34 (2) ◽  
pp. 353-363
Author(s):  
F. Kanwal ◽  
A. Batool ◽  
R. Akbar ◽  
S. Asim ◽  
M. Saleem
Keyword(s):  
Oxygen Evolution ◽  
Oxygen Evolution Reaction ◽  
Large Scale ◽  
Low Cost ◽  
High Surface ◽  
High Surface Area ◽  
Three Dimensional ◽  
Alkaline Electrolyte ◽  
Hydrogen Electrode ◽  
Molar Ratios

Electrochemical water splitting is the most promising pathway to produce high-purity hydrogen to alleviate global energy crisis. This reaction demands inexpensive, efficient and robust electrocatalyst for its commercial use. Herein, we demonstrate an effective, facile and scalable method for the synthesis of cerium doped Ni3Fe nanostructures as an electrocatalyst for oxygen evolution reaction (OER) by following simple chemical bath deposition route. The different molar ratios (3, 6 and 12 mM) of cerium in the chemical bath were used to study its effect on the structural and the electrochemical properties of the Ni3Fe nanostructured films. Doping of cerium contents induced variations in the morphology of deposited Ni3Fe nanostructures. The optimized electrocatalyst Ni3Fe/Ce-6 yielded high surface area catalyst nanosheets uniformly deposited on three-dimensional conductive scaffold to ensure increase in the exposure of doped Ni3Fe catalytic sites with high electrical conductivity. As a result, this earth-abundant electrocatalyst affords high OER performance with a small overpotential of 310 mV versus reversible hydrogen electrode (RHE) at 10 mA cm-2 and retains good stability up to ~ 10 h in alkaline electrolyte. This scalable strategy has great potential in future advancement of efficient and low-cost electrocatalysts for their large-scale application in energy conversion systems.                     KEY WORDS: Oxygen evolution, Electrocatalyst, Ni3Fe nanostructures, Cerium, Alkaline electrolyte   Bull. Chem. Soc. Ethiop. 2020, 34(2), 353-363 DOI: https://dx.doi.org/10.4314/bcse.v34i2.12

scholarly journals Recent Advances in Oxygen Electrocatalysts Based on Perovskite Oxides

Nanomaterials ◽  
2019 ◽  
Vol 9 (8) ◽  
pp. 1161 ◽  
Author(s):  
Jun Xu ◽  
Chan Chen ◽  
Zhifei Han ◽  
Yuanyuan Yang ◽  
Junsheng Li ◽  
...  
Keyword(s):  
High Performance ◽  
Low Cost ◽  
High Surface ◽  
High Surface Area ◽  
Precious Metals ◽  
Perovskite Oxides ◽  
Air Battery ◽  
Energy Conversion Devices ◽  
Further Development ◽  
Electrochemical Oxygen

Electrochemical oxygen reduction and oxygen evolution are two key processes that limit the efficiency of important energy conversion devices such as metal–air battery and electrolysis. Perovskite oxides are receiving discernable attention as potential bifunctional oxygen electrocatalysts to replace precious metals because of their low cost, good activity, and versatility. In this review, we provide a brief summary on the fundamentals of perovskite oxygen electrocatalysts and a detailed discussion on emerging high-performance oxygen electrocatalysts based on perovskite, which include perovskite with a controlled composition, perovskite with high surface area, and perovskite composites. Challenges and outlooks in the further development of perovskite oxygen electrocatalysts are also presented.

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