In situ exsolution of Ag from AgBiS2 nanocrystal anode boosting high-performance potassium-ion batteries

2020 ◽  
Vol 8 (30) ◽  
pp. 15058-15065
Author(s):  
Xiaoru Ren ◽  
Dongxu Yu ◽  
Long Yuan ◽  
Yaocai Bai ◽  
Keke Huang ◽  
...  
Keyword(s):  
High Performance ◽  
Potassium Ion

In situ Ag exsolution from AgBiS2 nanocrystals as an intermediate charge transmitter assists cycling for K+ intercalation in anode reactions.

Precise Synthesis of Pillared Graphene Nanosheets with Superior Potassium Storage via In-situ Growth Strategy

2021 ◽  
Author(s):  
Xiaohua Qiao ◽  
Lixia Sun ◽  
Jianhua Sun ◽  
chaoyang Hou ◽  
shuaijuan Bian ◽  
...  
Keyword(s):  
High Performance ◽  
Graphene Nanosheets ◽  
Reversible Capacity ◽  
Potassium Ion ◽  
Growth Strategy ◽  
Electrochemical Potential ◽  
In Situ Growth ◽  
Resource Abundance

Potassium ion batteries (PIBs) have been drawn much interest because of the resource-abundance and tempting electrochemical potential of potassium. However, developing high-performance anodes for PIBs with superior reversible capacity and...

High performance Nanogold™-in situ hybridzation and its use in the detection of hybridized and PCR-amplified microscopical preparations

1996 ◽  
Vol 54 ◽  
pp. 896-897
Author(s):  
G. W. Hacker ◽  
I. Zehbe ◽  
J. Hainfeld ◽  
A.-H. Graf ◽  
C. Hauser-Kronberger ◽  
...  
Keyword(s):  
Polymerase Chain Reaction ◽  
Messenger Rna ◽  
High Performance ◽  
Detection System ◽  
Direct Methods ◽  
Genetic Alterations ◽  
Chain Reaction ◽  
Protein Encoding ◽  
Polymerase Chain

In situ hybridization (ISH) with biotin-labeled probes is increasingly used in histology, histopathology and molecular biology, to detect genetic nucleic acid sequences of interest, such as viruses, genetic alterations and peptide-/protein-encoding messenger RNA (mRNA). In situ polymerase chain reaction (PCR) (PCR in situ hybridization = PISH) and the new in situ self-sustained sequence replication-based amplification (3SR) method even allow the detection of single copies of DNA or RNA in cytological and histological material. However, there is a number of considerable problems with the in situ PCR methods available today: False positives due to mis-priming of DNA breakdown products contained in several types of cells causing non-specific incorporation of label in direct methods, and re-diffusion artefacts of amplicons into previously negative cells have been observed. To avoid these problems, super-sensitive ISH procedures can be used, and it is well known that the sensitivity and outcome of these methods partially depend on the detection system used.

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