Archive for the ‘Hot Articles’ Category

An enzymatic Rube Goldberg machine: a bioluminescent switch for the detection of uracil DNA-glycosylase

A team of researchers from Shandong Normal University in Jinan, China, have developed a highly sensitive and label-free assay for the detection of uracil-DNA glycosylase, a DNA repair enzyme that removes uracil from DNA molecules. Uracil is an RNA base, and when uracil appears in DNA through deamination of cytosine or misincorporation during DNA synthesis, the error can have mutagenic consequences.

Diminished activity of uracil-DNA glycosylase has been linked to a number of disease states including human immunodeficiency and Bloom syndrome, an inherited disorder associated with an increased risk of cancer (among other symptoms). Developing sensitive methods to quantify uracil-DNA glycosylase would enable early diagnosis of such conditions and improve understanding of the DNA-repair machinery. As a proof-of-concept, the researchers showed that this method could quantify the enzyme in the cell lysate of HeLa cancer cells.

Their method reminds me of Rube Goldberg machines, which achieve a task via a series of connected, mechanical steps. Completion of one step triggers the start of another: such as a line of falling dominos hitting a marble that, in turn, rolls down a track. In this work the action of one enzyme returns a product that is the preferred substrate of another enzyme. At the risk of deviating slightly, one of the more spectacular examples of a Rube Goldberg machine is seen in the music video for OK GO’s ‘this too shall pass’, a single-take shoot of a warehouse sized machine, featuring rolling cars, swinging pianos, flowing water and rolling billiard balls, all to perform the task of (spoiler alert) blasting the band members in the face with coloured paint.

The label-free strategy for detecting uracil-DNA glycosylase results in a bioluminescent signal via tricyclic signal amplification

The strategy starts with the action of uracil-DNA glycosylase and ends with a bioluminescent signal via a cascade of enzymatic reactions

The authors’ strategy involves a series of sequential steps employing seven different enzymes and three nucleic acid probes. It begins with a double stranded DNA probe containing one rogue uracil base: the perfect bait for uracil-DNA glycosylase. The action of this enzyme and two others, in a process involving base excision, DNA backbone cleavage and the addition of thymine-rich sequences, produces a large quantity of single-stranded DNA molecules with long thymine-rich tails. These molecules hybridise with adenine-rich RNA probes to generate RNA-DNA duplexes. An enzyme digests the RNA portion, releasing adenosine monophosphate monomers, which are converted to adenosine triphosphate (ATP), a required energy input to activate firefly luciferase. Luciferase catalyses the oxidation of luciferin to form oxyluciferin, accompanied by a large bioluminescent signal. Thus, uracil-DNA glycosylase is detected with 1-2 orders of magnitude more sensitivity than state-of-the-art fluorescent and luminescent assays.

Unlike conventional Rube Goldberg machines, which are characterised by unnecessary complexity, in this ‘enzymatic Rube Goldberg machine’ each step has a specific purpose and serves to amplify the signal of the last. This is dubbed ‘tricyclic cascade signal amplification’ and it enables highly sensitive detection of the enzyme.

To find out more please read:

Label-free and high-throughput bioluminescence detection of uracil-DNA glycosylase in cancer cells through tricyclic cascade signal amplification

Yan Zhang, Qing-nan Li, Chen-chen Li, Chen-yang Zhang.
Chem. Commun., 2018, 54, 6991-6994
DOI: 10.1039/c8cc03769h

About the author

Zoë Hearne is a PhD candidate in chemistry at McGill University in Montréal, Canada, under the supervision of Professor Chao-Jun Li. She hails from Canberra, Australia, where she completed her undergraduate degree. Her current research focuses on transition metal catalysis to effect novel transformations, and out of the lab she is an enthusiastic chemistry tutor and science communicator.

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

HOT ChemComm articles for June

All of the referee-recommended articles below are free to access until 3rd August 2018.

Highly Lewis acidic cationic alkaline earth metal complexes 
Jürgen Pahl, Steffen Brand, Holger Elsen and Sjoerd Harder
Chem. Commun., 2018, Advance Article
DOI: 10.1039/C8CC04083D, Communication

_____________________________________________

Single-site labeling of lysine in proteins through a metal-free multicomponent approach
Maheshwerreddy Chilamari, Neetu Kalra, Sanjeev Shukla and Vishal Rai
Chem. Commun., 2018,54, 7302-7305
DOI: 10.1039/C8CC03311K, Communication

_____________________________________________

Controlling the growth of fullerene C60 cones under continuous flow
Ibrahim K. Alsulami, Thaar M. D. Alharbi, David P. Harvey, Christopher T. Gibson and Colin L. Raston
Chem. Commun., 2018, Advance Article
DOI: 10.1039/C8CC03730B, Communication

_____________________________________________

Formal water oxidation turnover frequencies from MIL-101(Cr) anchored Ru(bda) depend on oxidant concentration
Asamanjoy Bhunia, Ben A. Johnson, Joanna Czapla-Masztafiak, Jacinto Sá and Sascha Ott
Chem. Commun., 2018, Advance Article
DOI: 10.1039/C8CC02300J, Communication

_____________________________________________

Smart urea ionic co-crystals with enhanced urease inhibition activity for improved nitrogen cycle management
Lucia Casali, Luca Mazzei, Oleksii Shemchuk, Kenneth Honer, Fabrizia Grepioni, Stefano Ciurli, Dario Braga and Jonas Baltrusaitis
Chem. Commun., 2018,54, 7637-7640
DOI: 10.1039/C8CC03777A, Communication

_____________________________________________

CO2-Triggered microreactions in liquid marbles
Xinjie Luo, Hongyao Yin, Xian’e Li, Xin Su and Yujun Feng
Chem. Commun., 2018, Advance Article
DOI: 10.1039/C8CC01786G, Communication

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

Better Make It A Double

Synthesizing nanomaterials consisting of two-particle pairs, or dimers, is no longer a headache. Hongyu Chen and coworkers from Nanjing Tech University, China recently developed a protocol that can produce gold dimers with a record high yield. This breakthrough is published in Chem. Commun.

Dimers are suitable platforms to study the effects of particle-particle interactions on the electrical and optical properties of the constituent materials. Unfortunately, no conventional synthesis methods to exclusively produce dimers from single particles have been successful. This is because of the uncontrollable particle-aggregation rate that leads to the formation of multi-particle clusters. Therefore, how to couple single particles into dimers without triggering their further aggregation has become a tough nut to crack.

Chen and coworkers found a solution by developing a polymer-assisted method that generates gold dimers with high yield. Firstly, they encapsulated individual gold nanoparticles with polymer shells made of polystyrene-b-poly(acrylic acid). Under optimized conditions, the gold nanoparticles were mostly coupled into dimers (Figure 1), achieving a dimer yield of 65%. This is the highest dimer yield achieved for one-step synthesis methods.

Figure 1. (a) A transmission electron microscopy (TEM) image of the polymer-encapsulated gold single particles. (b) A TEM image and (c) a scanning electron microscopy image of the synthesized gold dimers. All scale bars are 200 nm.

The key to this success is due to three factors: temperature, solvent composition and acid concentration. All these factors can change the strength of the repulsion force among the polymer shells. The force must be meticulously tuned to a level that is weak enough to induce 1-to-1 coupling, but strong enough to prevent 1-to-multiple or multiple-to-multiple aggregation. Through a set of control experiments, the authors identified the optimal conditions to be 60 oC, dimethylformamide/water (v/v)=6:1 and 5 mM of hydrochloric acid.

The method demonstrated herein could be extended to other particles. It may also inspire versatile synthesis strategies towards complex nanostructures with high selectivity.

 

To find out more please read:

Controllable Oligomerization: Defying Step-Growth Kinetics in the Polymerization of Gold Nanoparticles

Xuejun Cheng, Gui Zhao, Yan Lu, Miao Yan, Hong Wang and Hongyu Chen

Chem. Sci., 2018, DOI: 10.1039/C8CC03424A

 

About the blogger:

Tianyu Liu obtained his Ph.D. (2017) in Physical Chemistry from University of California, Santa Cruz in the United States. He is passionate about scientific communication to introduce cutting-edge research to both the general public and scientists with diverse research expertise. He is a blog writer for Chem. Commun. and Chem. Sci. More information about him can be found at http://liutianyuresearch.weebly.com/.

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

HOT ChemComm articles for May

All of the referee-recommended articles below are free to access until 6th July 2018.

A quasi-solid-state and self-powered biosupercapacitor based on flexible nanoporous gold electrodes
Xinxin Xiao and Edmond Magner
Chem. Commun., 2018, 54, 5823-5826
DOI: 10.1039/C8CC02555J, Communication

_______________________________________________________________

Late stage modifications of P-containing ligands using transition-metal-catalysed C–H bond functionalisation
Zhuan Zhang, Pierre H. Dixneuf and Jean-François Soulé
Chem. Commun., 2018, Advance Article
DOI: 10.1039/C8CC02821D, Feature Article

_______________________________________________________________

A novel three-fluorophore system as a ratiometric sensor for multiple protease detection
Yana Okorochenkova, Martin Porubský, Sandra Benická and Jan Hlaváč
Chem. Commun., 2018, Advance Article
DOI: 10.1039/C8CC01731J, Communication

_______________________________________________________________

The environmental-sensitivity of a fluorescent ZTRS–Cd(II) complex was applied to discriminate different types of surfactants and determine their CMC values
Fei Deng, Shuangshuang Long, Qinglong Qiao and Zhaochao Xu
Chem. Commun., 2018, Advance Article
DOI: 10.1039/C8CC03888K, Communication

_______________________________________________________________

An intrinsically compressible and stretchable all-in-one configured supercapacitor
Mengmeng Hu, Jiaqi Wang, Jie Liu, Jiaheng Zhang, Xing Ma and Yan Huang
Chem. Commun., 2018, Advance Article
DOI: 10.1039/C8CC03375G, Communication

_______________________________________________________________

Paraffinic metal–organic polyhedrons: solution-processable porous modules exhibiting three-dimensional molecular order
Kenichiro Omoto, Nobuhiko Hosono, Mika Gochomori and Susumu Kitagawa
Chem. Commun., 2018, Advance Article
DOI: 10.1039/C8CC03705A, Communication

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

Come for the colour changing crystals, stay for the science

Synthesis of copper bimetallic complexes from imidazolyl ligands, and the solvatochromic materials formed upon crystallization and solvent guest-exchange. The solvatochromic behaviour was quantified with visible-region diffuse reflectance spectra.

Synthesis of copper bimetallic complexes from imidazolyl ligands, and the solvatochromic materials formed upon crystallization and solvent guest-exchange. The solvatochromic behaviour was quantified with visible-region diffuse reflectance spectra.

During the first inorganic chemistry course I took during my undergraduate degree, our professor started the class by passing around some mineral samples, promising us that if we pursued the chemistry of metals we could work with beautifully coloured crystals every day. At the time, colour seemed like such a trite detail amongst the complexity of the subject. Why would you choose a field of study based on something so simple? Well, after a PhD dominated by pale yellow oils, I think I get it now.

Nikolayenko and Barbour at the University of Stellenbosch in South Africa bring us colour! The authors synthesised organometallic copper complexes, which crystallise to form porous single crystals that drastically change colour upon absorption of various solvents. The authors investigated the solvatochromic mechanism using X-ray crystallography, EPR, UV-visible spectroscopy and DFT calculations. Solvatochromic materials are not just made to look pretty; they have potential to be used as sensitive, selective and recyclable sensors to detect solvent vapours with useful applications in industrial process risk management, chemical threat detection and environmental monitoring.

The researchers synthesised a series of complexes comprised of a bidentate ligand with 2-methylimidazolyl groups coordinated to copper(II) ions. The complexes stack to form channels in the crystal, capable of trapping solvent molecules to give different coloured crystals: DMSO and THF-containing crystals are green (λmax = 574 nm and 540 nm, respectively), those containing acetonitrile are red (λmax = 624 nm), and crystals trapping acetone, ether and pentane are yellow (λmax = 588), orange (λmax = 598 nm) and red/brown (λmax = 592 nm), respectively.

The authors revealed a correlation between the size of the solvent guest, coordination geometry of the copper complex, and the ligand field splitting. Small guests such as acetonitrile minimally perturb the metallocyclic framework, preserving a rhombic ligand field geometry (large δxy of g values in the EPR spectrum), small ligand d-orbital splitting and red-shifted optical spectra. Large guests such as THF have the opposite effect, giving ligand field geometries approaching tetragonal (small δxy), large ligand field d-orbital splitting and blue-shifted optical spectra.

By delving into the complexity beneath a seemingly simple phenomenon, Nikolayenko, Barbour and their co-workers have shown using a series of single-crystal complexes that there is nothing simple about colour (and nothing trite about detail).

To find out more please read:

Supramolecular solvatochromism: mechanistic insight from crystallography, spectroscopy, and theory

Varvara I. Nikolayenko, Lisa M. van Wyk, Orde Q. Munro, Leonard J. Barbour.
Chem. Commun., 2018, Advance Article
DOI: 10.1039/c8cc02197j

About the author

Zoë Hearne is a PhD candidate in chemistry at McGill University in Montréal, Canada, under the supervision of Professor Chao-Jun Li. She hails from Canberra, Australia, where she completed her undergraduate degree. Her current research focuses on transition metal catalysis to effect novel transformations, and out of the lab she is an enthusiastic chemistry tutor and science communicator.

 

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

Pt3Ni-Coated Palladium Nano-branches Outperformed Pt in Catalyzing Ethanol Oxidation

Researchers in China recently developed a new Pd-based catalyst that outperformed Pt, the benchmark catalyst for electrochemical oxidation of ethanol. This catalyst, synthesized by a one-pot chemical reduction method, consists of branched Pd nanocrystals coated with thin Pt3Ni shells.

The ethanol oxidation reaction (EOR) is a typical anode reaction that drives the energy output from fuel cells. Due to its intrinsically slow kinetics, the reaction requires proper EOR catalysts to facilitate the oxidation. Pt-based materials are highly active in promoting EOR, but the scarcity of Pt leads to high costs and demands efficient methods to recycle these materials. In addition, the instable catalytic activity of Pt significantly reduces the lifetime of EOR catalysts containing Pt. Clearly, developing inexpensive EOR catalysts with comparable performance to Pt is meaningful for the affordability and durability of fuel cells.

A research team led by Shuifen Xie at Huaqiao University and Shenzhen Research Institute of Xiamen University in China, have demonstrated a one-pot chemical reduction method of a novel EOR catalyst. This catalyst is made of Pt3Ni-coated Pd nanocrystals as shown in Figure 1. There are three main advantages for this catalyst over the benchmark Pt: Firstly, the core material Pd is more affordable. Secondly, the ultrathin Pt-alloy coating, Pt3Ni, contains relatively less Pt and is reported to exhibit high EOR catalytic activity. Thirdly, the little lattice mismatch between Pt and Pd allows seamless integration of the two metals that is beneficial to preserve the structural integrity and ensure excellent durability.

Figure 1. (a) The schematic illustration showing the key steps of the one-pot chemical reduction method. The catalyst is formed via consecutive reduction of Pd2+, Pt2+ and Ni2+ to Pd nano-branches, Pt nanoparticles and Pt3Ni coatings, respectively. (b) A TEM image of a representative morphology of a branched nanocrystal. (c) Elemental mappings depict that Pt and Ni elements exist mainly in the shell while Pd is in the core.

Electrochemical characterizations revealed that the catalytic performance of the Pt3Ni-coated Pd nanocrystals outperformed those of two commercial catalysts: Pt/C (Pt particles supported on activated carbon) and Pd black (a fine powder elemental Pd). Figure 2a compares the linear-sweep voltammograms of the three samples. The synthesized catalyst showed appreciably enhanced oxidation current at potentials beyond 0.4 V vs. RHE. The histograms in Figure 2b clearly display that the mass activity and the specific activity of the synthesized nanocrystals are the highest. The authors ascribed the superior performance to the high surface area (42.50 m2 g-1), the ultrathin Pt3Ni coating with its {111} crystal planes exposed, and the core-shell configuration.

Figure 2. (a) Linear-sweep voltammograms of the synthesized catalyst (Pd@Pt3Ni/C), Pt/C and Pd black. (b) The comparison of mass activity (i.e. oxidation current normalized to the masses of the catalysts) and specific activity (i.e. oxidation current normalized to the areas of the catalysts) of Pd@Pt3Ni/C, Pt/C and Pd black.

This work signifies the feasibility of Pd-based nano-catalysts as alternatives to Pt towards catalyzing EOR. It is also expected to encourage the effort in developing a diverse array of inexpensive and high-performance catalysts for other reactions pertaining to fuel cells, including but not limited to oxidation of fuels other than ethanol and oxygen reduction reactions.

To find out more please read:

One-Pot Synthesis of Pd@Pt3Ni Core-Shell Nanobranches with Ultrathin Pt3Ni{111} Skins for Efficient Ethanol Electrooxidation

Yuanyuan Wang, Wei Wang, Fei Xue, Yong Cheng, Kai Liu, Qiaobao Zhang, Maochang Liu and Shuifen Xie

Chem. Commun., 2018, DOI: 10.1039/c8cc02816h

About the blogger:

Tianyu Liu obtained his Ph.D. (2017) in Physical Chemistry from University of California, Santa Cruz in the United States. He is passionate about scientific communication to introduce cutting-edge research to both the general public and scientists with diverse research expertise. He is a blog writer for Chem. Commun. and Chem. Sci. More information about him can be found at http://liutianyuresearch.weebly.com/.

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

The CO2-Capturing Mechanism of Quaternary Nitrogen-Containing Polymers Revealed Experimentally

A group of scientists from Washington University at St. Louis, USA have disclosed experimentally how CO2 is captured by polymers with quaternary nitrogen cations. Using solid-state nuclear magnetic resonance (NMR), the authors established that CO2 molecules were absorbed as bicarbonate anions (HCO3).

The increasing amount of CO2 has posed a number of concerning environmental issues such as climate change, rising sea level and ocean acidification. Capturing CO2 from the atmosphere is an effective way to lower the CO2 concentration. Recently, a family of polymer absorbents containing quaternary nitrogen functional groups, termed humidity-swing polymers, have been identified as promising absorbents to absorb CO2 directly from air. However, the limited understanding of the chemical mechanism related to their CO2-capturing capability hindered the development of these promising absorbents.

In ChemComm, Yang et al. used solid-state 13C NMR to explore how CO2 molecules were captured and released. Figure 1a presents the NMR spectra of a humidity-swing polymer absorbent itself (top), upon contacting with CO2 (middle) and after releasing CO2 (bottom). The most striking feature is the appearance of an additional sharp peak at a chemical shift of 161 ppm in the middle spectrum, which did not show up in the other two spectra. The authors further studied the shape evolution of the additional peak, with respect to temperature, and concluded that the peak was due to HCO3 anions. Additionally, the authors also identified the presence of hydroxide anions in the absorbent after CO2 was released.

Figure 1. (a) The solid-state 13C NMR spectra of the humidity-swing polymeric absorbent (structure shown in the inset of the middle spectrum) itself (top), upon contacting with CO2 (middle) and after releasing CO2 (bottom). (b) The proposed pathways of how CO2 molecules interact with the quaternary-N anions of the absorbent.

The researchers then proposed the CO2 adsorption-desorption mechanism (illustrated in Figure 1b) based on the experimental results. The storage and release of CO2 depend on the humidity level of the surroundings: When the humidity is low, the polymer absorbs CO2 and forms HCO3 anions; the negative charge of HCO3 is counter-balanced by the neighboring quaternary N cations. When the humidity is increased, HCO3 anions combine with water and decompose to CO2 and hydroxide anions. This proposed pathway does not involve CO32- anions, which differs from the previously-reported mechanisms derived from theoretical simulations.

The published results represent the first set of experimental evidence elucidating how CO2 molecules interact with humidity-swing polymeric absorbents. The acquired mechanistic insight could provide valuable guidelines for the design of CO2 absorbents with ultrahigh absorption capacity.

 

To find out more please read:

Humidity-Swing Mechanism for CO2 Capture from Ambient Air
Hao Yang, Manmilan Singh and Jacob Schaefer
Chem. Commun., 2018, DOI: 10.1039/c8cc02109k

About the blogger:

Tianyu Liu obtained his Ph.D. (2017) in Physical Chemistry from University of California, Santa Cruz in United States. He is passionate about scientific communication to introduce cutting-edge research to both the general public and scientists with diverse research expertise. He is a blog writer for Chem. Commun. and Chem. Sci. More information about him can be found at http://liutianyuresearch.weebly.com/.

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

Read our most cited ChemComm Features from 2016 and 2017

We are showcasing our 20 most cited ChemComm Feature articles from 2016 and from 2017. This collection provides an easy way to access some of the most exciting topics of research across the chemical sciences – from materials and supramolecular chemistry through to physical chemistry and catalysis.

ALL articles are FREE to read and download until 11 June!

We hope you enjoy reading this collection! Some of the highlights are given below:

 

C6CC05568K graphical abstract, Atomic and molecular layer deposition: off the beaten track, van Ommen et al.Atomic and molecular layer deposition: off the beaten track

 

Van Bui, F. Grillo and J. R. van Ommen

Chem. Commun., 2017, 53, 45-71

DOI: 10.1039/C6CC05568K
 

 

 


C6CC08967D Graphical Abstract, Biological and related applications of pillar[n]arenes, Wang et al.

Biological and related applications of pillar[n]arenes

 

CuhaWijay Sathiyajith, Rafik Rajjak Shaikh, Qian Han, Yue Zhang, Kamel Meguellati and Ying-Wei Yang

Chem. Commun., 2017, 53, 677-696

DOI: 10.1039/C6CC08967D

 

 


C5CC08213G Graphical Abstract, Boron clusters in luminescent materials, Mukherjee and ThilagarBoron clusters in luminescent materials

 

Sanjoy Mukherjee and Pakkirisamy Thilagar

Chem. Commun., 2016, 52, 1070-1093

DOI: 10.1039/C5CC08213G

 

 

 


Fluorescent glycoprobes: a sweet addition for improved sensing

C6CC06875H Graphical Abstract, Fluorescent glycoprobes: a sweet addition for improved sensing, Xie et al.

 

Xiao-Peng He, Yi Zang, Tony D. James, Jia Li, Guo-Rong Chen
and Juan Xie

Chem. Commun., 2017, 53, 82-90

DOI: 10.1039/C6CC06875H

 

 

 


C6CC03638D Graphical Abstract, Halogen bonding anion recognition, Brown and Beer

Halogen bonding anion recognition

 

Asha Brown and Paul D. Beer

Chem. Commun., 2016, 52, 8645-8658

DOI: 10.1039/C6CC03638D

 

 

 


C6CC08820A Graphical Abstract, Long range electrostatic forces in ionic liquids, Atkin et al.Long range electrostatic forces in ionic liquids

 

Matthew A. Gebbie, Alexander M. Smith, Howard A. Dobbs, Alpha A. Lee,
Gregory G. Warr, Xavier Banquy, Markus Valtiner, Mark W. Rutland, Jacob N. Israelachvili,
Susan Perkin and Rob Atkin

Chem. Commun., 2017, 53, 1214-1224

DOI: 10.1039/C6CC08820A

 

 


C5CC08216A Graphical Abstract, Pharmaceutical cocrystals: along the path to improved medicines, Zaworotko et al.Pharmaceutical cocrystals: along the path to improved medicines

 

Naga K. Duggirala, Miranda L. Perry, Örn Almarsson and Michael J. Zaworotko

Chem. Commun., 2016, 52, 640-655

DOI: 10.1039/C5CC08216A

 

 

 


C6CC00336B Graphical Abstract, Rational control of nano-scale metal-catalysts for biomass conversion, Yan et al.Rational control of nano-scale metal-catalysts for biomass conversion

 

Yunzhu Wang,  Sudipta De  and  Ning Yan

Chem. Commun., 2016, 52, 6210-6224

DOI: 10.1039/C6CC00336B

 

 

ChemComm is renowned as the fastest publisher of articles providing information on new avenues of research, drawn from all the world’s major areas of chemical research. ChemComm is the ideal place to publish your research.

 

Submit your urgent research to ChemComm today!

 

Stay up to date with ChemComm
Be among the first to hear about the newest articles being published – Sign-up to our journal news alert to receive information about most read articles, themed issues, journal news, as well as calls for papers and invitations.

 

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

Ruthenium Currency for a Hydrogen Fuel Economy

A group of researchers at the Chinese Academy of Sciences and Southwest University want us to kick the fossil fuels habit. Their research comes to us from China, a country using roughly one quarter of the world’s yearly energy consumption, and where the finite nature of fossil fuels is a very real threat to energy supply security. Leading in energy use, China also leads the world in electricity production from renewable sources and investment in clean energy projects.

Hydrogen is considered a viable alternative to fossil fuels as it is energy rich, more so than petrol or ethanol at 39 kWh/kg (petrol: 13 kWh/kg, ethanol: 8.2 kWh/kg), and upon combustion emits only water vapour. However, hydrogen is often obtained from fossil fuels, and it will only be a practical option for the world’s future energy needs if it can be produced from a renewable source.

Preparation of the Ru2P/reduced graphene oxide electrocatalyst for the hydrogen evolution reaction

Preparation of the Ru2P/reduced graphene oxide catalyst

To this end, water splitting offers a solution. In a water electrolysis cell, hydrogen is produced at the cathode via the hydrogen evolution reaction (HER, 2H+ + 2e –> H2), and molecular oxygen is produced at the anode (2H2O –> O2 + 4H+ + 4e). It is ideal in theory, but high energy efficiencies are required to make water splitting viable, and this relies on the development of catalytic electrodes to minimize overpotentials required to drive the reaction. Currently, state of the art HER electrocatalysts use platinum, which is expensive and rare. Furthermore, platinum catalysts are most efficient in an acidic electrolyte and proceed 2-3 times slower in alkaline solutions. On the other hand, the best oxygen evolution catalysts perform better in alkaline environments. Using an alkaline electrolyte has overall advantages as it is less corrosive, thus increasing the stability and lifetime of the electrolytic cell.

The authors have developed a HER catalyst, using ruthenium, with overpotentials and current densities superior to Pt/C in both alkaline and acidic conditions.

DFT calculation to probe the hydrogen adsorption energies on the active catalytic surface of the Ru2P on reduced graphene oxide catalyst.

DFT calculation to probe the hydrogen adsorption energies on the active catalytic surface of the Ru2P catalyst. a) and b) front and side views of the calculated Ru2P/reduced graphene oxide surface. c) free energy diagram for the HER with different catalysts.

The electrocatalyst is comprised of small, uniform Ru2P nanoparticles (~2-4 nm) evenly distributed on reduced graphene oxide sheets. The activity of the prepared catalyst (1.0 mg cm-2) for the HER was measured in an acidic medium (0.5 M H2SO4) and the overpotential to achieve a current density of -10 mA cm-2 was -22 mV, superior to Pt/C (-27 mV). In an alkaline environment (1.0 M KOH) catalyst performance was enhanced, with an overpotential of -13 mV (29 mV lower than Pt/C). High Faradaic efficiencies of more than 98% were measured in both acidic and alkaline solutions. Additionally, analysis was undertaken to further understand how the structure and composition of the catalyst influences its activity. Double layer capacitance measurements gave clues about the catalyst surface, while theoretical DFT calculations were used to study H-adsorption energies.

There is no way to avoid the reality that ruthenium is also a rare and costly metal, and for this reason may not hold the key to solving our energy woes. However, of real value are the insights gained from probing the structure function relationship of this highly active catalyst, which may guide the synthesis of rationally-designed catalysts using inexpensive and abundant materials.

To find out more please read:

Ultrasmall Ru2P nanoparticles on graphene: a highly efficient hydrogen evolution reaction electrocatalyst in both acidic and alkaline media

Tingting Liu, Shuo Wang, Qiuju Zhang, Liang Chen, Weihua Hu, Chang Ming Li.
Chem. Commun., 2018, 54, 3343-3346
DOI: 10.1039/c8cc01166d

About the author:

Zoë Hearne is a PhD candidate in chemistry at McGill University in Montréal, Canada, under the supervision of Professor Chao-Jun Li. She hails from Canberra, Australia, where she completed her undergraduate degree. Her current research focuses on transition metal catalysis to effect novel transformations, and out of the lab she is an enthusiastic chemistry tutor and science communicator.

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

In-Situ Electron Paramagnetic Resonance Spectroscopy Revealed the Charge Storage Behavior of Activated Carbon

Recently in Chem. Commun., Wang et al. from University of Manchester and Liverpool John Moores University, U.K. demonstrated that in-situ electron paramagnetic resonance (EPR) spectroscopy was a powerful tool to study the charge storage mechanism of activated carbon.

Activated carbon is a type of microporous carbon used for electrodes of supercapacitors (a family of charge-storage devices similar to batteries). Conventional electrochemical testing techniques (e.g. cyclic voltammetry) are able to evaluate the overall performance of electrode materials but are unable to reveal the charge storage mechanism at the atomic level. Understanding the charge storage mechanism is crucial to guide the design and synthesis of electrode materials with improved performance. During the past decade, the development of numerous in-situ probing techniques has allowed materials researchers to explore the microscopic charge-discharge behaviour of supercapacitor electrodes.

In the published paper, in-situ EPR spectroscopy was used to study the electrochemical properties of activated carbon under different external potentials. EPR is very sensitive to electron spins originating from unpaired electrons that are generated upon charging or discharging electrode materials. This characteristic makes EPR a suitable technique for in-situ studies. To carry out the experiments, the authors designed and constructed a capillary three-electrode testing cell (Figure 1a). This cell was placed in an EPR spectrometer and its activated carbon electrode was connected to an external power source (to apply external potentials to the activated carbon electrode). The authors collected the spectra of the activated carbon electrode at selected applied potentials, an example of which is shown in Figure 1b.

Analysis of the obtained spectra offered important information about how the surface of activated carbon changed at different potentials. Specifically, the authors deconvoluted the signal into two components: the narrow signal and the broad signal corresponding to the blue and red curves in Figure 1b, respectively. The peak intensity of the narrow signal increased drastically when charging the electrode, but remained almost unchanged when altering the testing temperature. This observation suggests that the origin of the narrow peaks was the surface-localized electrons. These localized electrons were likely from the oxidized products (i.e. radicals) of carboxylate and alkoxide groups on the surface of the activated carbon, evolved during the charging process. The broad signal was ascribed to electrons located on aromatic units (e.g. graphene domains) and its intensity was found to be proportional to the number of ions electrically adsorbed on the activated carbon surface.

Figure 1. (a) The structure of the self-built capillary three-electrode cell: CE – counter electrode (Pt wire); RE – reference electrode (Ag/AgCl); WE – working electrode (activated carbon). (b) A typical EPR signal (black) that can be deconvoluted into narrow peaks (blue) and broad peaks (red).

This work highlights EPR spectroscopy as a novel tool for in-situ investigation of the charge-storage mechanism of carbon-based supercapacitor electrodes, and could be potentially extended to study other types of materials. The availability of diverse in-situ techniques is expected to provide more in-depth fundamental understanding that will guide researchers to rationally develop electrodes with optimized performance.

 

To find out more please read:

In-Situ Electrochemical Electron Paramagnetic Resonance Spectroscopy as A Tool to Probe Electric Double Layer Capacitance

Bin Wang, Alistair J. Fielding and Robert A. W. Dryfe

Chem. Commun. 2018, DOI: 10.1039/c8cc00450a

About the blogger:

Tianyu Liu obtained his Ph.D. (2017) in Physical Chemistry from University of California, Santa Cruz in United States. He is passionate about scientific communication to introduce cutting-edge research to both the general public and scientists with diverse research expertise. He is an online blog writer for Chem. Commun. and Chem. Sci. More information about him can be found at http://liutianyuresearch.weebly.com/.

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)