Selection of Negative Charged Acidic Polar Additives to Regulate Electric Double Layer for Stable Zinc Ion Battery

Zinc-ion batteries are promising for large-scale electrochemical energy storage systems,which still suffer from interfacial issues,e.g.,hydrogen evolution side reaction(HER),self-corrosion,and uncontrollable dendritic Zn electrodeposition.Although the regulation of electric double layer(EDL)has been verified for interfacial issues,the principle to select the additive as the regulator is still misted.Here,several typical amino acids with different characteristics were examined to reveal the interfacial behaviors in regulated EDL on the Zn anode.Negative charged acidic polarity(NCAP)has been unveiled as the guideline for selecting additive to reconstruct EDL with an inner zincophilic H_(2)O-poor layer and to replace H_(2)O molecules of hydrated Zn^(2+)with NCAP glutamate.Taking the synergistic effects of EDL regulation,the uncontrollable interface is significantly stabilized from the suppressed HER and anti-self-corrosion with uniform electrodeposition.Consequently,by adding NCAP glutamate,a high average Coulombic efficiency of 99.83%of Zn metal is achieved in Zn|Cu asymmetrical cell for over 2000 cycles,and NH4V4O10|Zn full cell exhibits a high-capacity retention of 82.1%after 3000 cycles at 2 A g^(-1).Recapitulating,the NCAP principle posted here can quicken the design of trailblazing electrolyte additives for aqueous Zn-based electrochemical energy storage systems.

The Existence of the Negative Charge of Gold in Sulphide Minerals and Its Formation Mechanism

Through a study, particularly an X-ray photoelectron spectroscopy (XPS or ESCA) analysis, of gold-bearing arsenopyrite and pyrite in Carlin-type gold deposits of Guangxi, China, and hydrothermally synthesized gold-bearing pyrite and marcasite, the authors have found that these minerals contain 'invisible gold' whose binding energy is lower than that of native gold (Au°). Therefore they suggest that gold occurs in a negative charge state in these sulphide minerals as it replaces some sulphur and is combined with sulphur with the covalent bond. This paper also preliminarily discusses the possibility of its formation from the chemistry and geochemistry of gold, crystal chemistry of arsenopyrite, pyrite and marcasite and geochemical environment.

Interaction Between Charge Characteristics and Cu^(2+) Adsorption-Desorption of Soils with Variable or Permanent Charge

Charge characteristics and Cu2+ adsorption-desorption of soils with variable charge (latosol) and permanent charge (brown soil) and the relationship between them were studied by means of back-titration and adsorption equilibrium respectively. The amount of variable negative charge was much less in variable-charge soil than in permanent-charge soil and increased with the pH in the system, but the opposite trend occurred in the points of zero charge (PZCs). The amount of Cu2+ ions sorbed by permanent-charge soil was more than that by variable-charge soil and increased with the increase of Cu2+ concentration within a certain range in the equilibrium solution. The amount of Cu2+ ions desorbed with KC1 from permanent-charge soil was more than that from variable-charge soil, but the amount of Cu2+ ions desorbed with de-ionized water from permanent-charge soil was extremely low whereas there was still a certain amount of desorption from variable-charge soil. The increase of PZC of soils with variable or permanent charge varied with the increment of Cu2+ ions added. When the same amount of Cu2+ ions was added, the increments of PZC and variable negative surface charge of permanent-charge soil were different from those of variable-charge soil.

AlO_x prepared by atomic layer deposition for high efficiency-type crystalline silicon solar cell

The influence of atomic layer deposition parameters on the negative charge density in AlOx film is investigated by the corona-charge measurement. Results show that the charge density can reach up to -1.56×10^12 cm%-2 when the thickness of the film is 2.4 nm. The influence of charge density on cell conversion efficiency is further simulated using solar cell analyzing software （PC1D）. With AlOx passivating the rear surface of the silicon, the cell efficiency of 20.66% can be obtained.

Ultra-small nanodots coated with oligopeptides providing highly negative charges to enhance osteogenic differentiation of hBMSCs better than osteogenic induction medium

For bone regenerative engineering,it is a promising method to form skeletal tissues differentiating from human bone morrow mesenchyme stem cells(hBMSCs).However,it is still a critical challenge to efficiently control ostogenesis and clearly reveal the influence factor.To this end,the fluorescent gold nanodots(Au NDs) with highly negative charges as osteogenic induction reagent are successfully synthesized,which display better than commercial osteogenic induction medium through the investigations of ALP activity(2.5 folds) and cytoskeleton staining(1.5 folds).Two kinds of oligopeptides with different bio-structures(cysteine,Cys and glutathione,GSH) are selected for providing surficial charges on Au NDs.It is revealed that Au-Cys with more negative charges(-51 mV) play better role than Au-GSH(-19 mV) in osteogenic differentiation,when both of them have same size(~2 nm),sphere shape and show similar cell uptake amount.To explore deeply,osteogenesis related signaling pathways are monitored,revealing that the enhancement of osteogenic differentiation was through autophagy signaling pathway triggered by Au-Cys.And the promotion of highly negative charges in osteogenic diffe rentiation was further proved via sliver nanodots(Ag NDs,Ag-Cys and Ag-GSH) and carbon nanodots(CDs,Cys-CDs and GSH-CDs).This work indicates part of insights during hBMSCs differentiation and provides a novel strategy in osteogenic differentiation process.

Interfacial high-concentration electrolyte for stable lithium metal anode:Theory,design,and demonstration

Lithium metal anodes hold great potential for high-energy-density secondary batteries.However,the uncontrollable lithium dendrite growth causes poor cycling efficiency and severe safety concerns,hindering lithium metal anode from practical application.Electrolyte components play important roles in suppressing lithium dendrite growth and improving the electrochemical performance of long-life lithium metal anode,and it is still challenging to effectively compromise the advantages of the conventional electrolyte(1 mol·L^(−1)salts)and high-concentration electrolyte(>3 mol·L^(−1)salts)for the optimizing electrochemical performance.Herein,we propose and design an interfacial high-concentration electrolyte induced by the nitrogen-and oxygen-doped carbon nanosheets(NO-CNS)for stable Li metal anodes.The NO-CNS with abundant surface negative charges not only creates an interfacial high-concentration of lithium ions near the electrode surface to promote chargetransfer kinetics but also enables a high ionic conductivity in the bulk electrolyte to improve ionic mass-transfer.Benefitting from the interfacial high-concentration electrolyte,the NO-CNS@Ni foam host presents outstanding electrochemical cycling performances over 600 cycles at 1 mA·cm^(−2) and an improved cycling lifespan of 1,500 h for symmetric cells.