Topic
Noble metal
About: Noble metal is a research topic. Over the lifetime, 15113 publications have been published within this topic receiving 337947 citations.
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TL;DR: In this paper, a series of nickel hydroxide-modified COF composite materials Ni(OH)2-X%/TpPa-2 (X: molar fraction of Ni)2 was designed and constructed by in-situ adding TpPa2 into the reaction system of Ni(O)2 and the resulting materials exhibit a novel sandwich-like morphology.
105 citations
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104 citations
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TL;DR: It is demonstrated here that the electrochemical generation of hydroxyl ions and hydrogen bubbles can be used to induce the synthesis of enzyme- or protein-encapsulated 3D porous silica structure on the surface of noble metal electrodes to fabricate biosensors and bioelectronic devices in situ.
Abstract: We demonstrate here that the electrochemical generation of hydroxyl ions and hydrogen bubbles can be used to induce the synthesis of enzyme- or protein-encapsulated 3D porous silica structure on the surface of noble metal electrodes. In the present work, the one-step synthesis of a glucose oxidase (GOD)-encapsulated silica matrix on a platinum electrode is presented. In this process, glucose oxidase was mixed with ethanol and TEOS to form a doped precursory sol solution. The electrochemically generated hydrogen bubbles at negative potentials assisted the formation of the porous structure of a GOD-encapsulated silica gel, and then the one-step immobilization of enzyme into the silica matrix was achieved. Scanning electron microscopy (SEM) and scanning electrochemical microscopy (SECM) characterizations showed that the GOD-encapsulated silica matrix adhered to the electrode surface effectively and had an interconnected porous structure. Because the pores started at the electrode surface, their sizes increased gradually along the distance away from the electrode and reached maximum at the solution side, and effective mass transport to the electrode surface could be achieved. The entrapped enzyme in the silica matrix retained its activity. The present glucose biosensor had a short response time of 2 s and showed a linear response to glucose from 0 to 10 mM with a correlation coefficient of 0.9932. The detection limit was estimated to be 0.01 mM at a signal-to-noise ratio of 3. The apparent Michaelis-Menten constant (K m app) and the maximum current density were determined to be 20.3 mM and 112.4 microA cm-2, respectively. The present method offers a facile way to fabricate biosensors and bioelectronic devices in situ.
104 citations
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TL;DR: A short review of the ALD growth of first-row transition metal films is given in this paper, where the current state of precursor and reducing co-reagent development is discussed and key future challenges are outlined.
104 citations
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TL;DR: In this article, a hollow porous Ag-Pt alloy nanoparticles with Pt coating are prepared via a facile controlled galvanic replacement reaction to reduce the dosage of noble metal Pt and improve the catalytic activity of the catalyst in fuel cells.
Abstract: Aiming to reduce the dosage of the noble metal Pt and improve the catalytic activity of the catalyst in fuel cells, hollow porous Ag–Pt alloy nanoparticles with Pt coating are prepared via a facile controlled galvanic replacement reaction. Ag is used as the substrate to build a hollow porous structure and alloyed with Pt to minimize the tensile effect of the Ag on the deposited Pt skin which would significantly lower the catalytic performance of the Ag–Pt bimetallic catalyst. This hollow porous Ag/Pt bimetallic catalyst exhibits a long catalytic durability and a mass activity of 0.438 A mgPt−1 at 0.9 V (vs. RHE) towards the oxygen reduction reaction (ORR), which is ca. 3 times higher than that of the commercial Pt/C catalyst. The significant enhancement over the state-of-the-art Pt catalysts can be attributed to (1) the high surface area of the nanoparticles, (2) the more suitable d-band center of the Pt skin deposited on the Ag–Pt alloy substrate, and (3) the high thermal stability of the Ag–Pt alloy. Therefore, this work provides a new strategy for designing high-performance catalysts with low cost. In addition, the synthetic chemistry involved can possibly be extended for fabricating versatile catalysts with a similar structure.
104 citations