<?xml version="1.0" encoding="UTF-8"?><rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcq="http://purl.org/dc/terms/"><records count="1" morepages="false" start="1" end="1"><record rownumber="1"><dc:product_type>Journal Article</dc:product_type><dc:title>Single-atomic platinum on fullerene C60 surfaces for accelerated alkaline hydrogen evolution</dc:title><dc:creator>Zhang, Ruiling; Li, Yaozhou; Zhou, Xuan; Yu, Ao; Huang, Qi; Xu, Tingting; Zhu, Longtao; Peng, Ping; Song, Shuyan; Echegoyen, Luis; Li, Fang-Fang</dc:creator><dc:corporate_author/><dc:editor/><dc:description>&lt;title&gt;Abstract&lt;/title&gt; &lt;p&gt;The electrocatalytic hydrogen evolution reaction (HER) is one of the most studied and promising processes for hydrogen fuel generation. Single-atom catalysts have been shown to exhibit ultra-high HER catalytic activity, but the harsh preparation conditions and the low single-atom loading hinder their practical applications. Furthermore, promoting hydrogen evolution reaction kinetics, especially in alkaline electrolytes, remains as an important challenge. Herein, Pt/C&lt;sub&gt;60&lt;/sub&gt;catalysts with high-loading, high-dispersion single-atomic platinum anchored on C&lt;sub&gt;60&lt;/sub&gt;are achieved through a room-temperature synthetic strategy. Pt/C&lt;sub&gt;60&lt;/sub&gt;-2 exhibits high HER catalytic performance with a low overpotential (η&lt;sub&gt;10&lt;/sub&gt;) of 25 mV at 10 mA cm&lt;sup&gt;−2&lt;/sup&gt;. Density functional theory calculations reveal that the Pt-C&lt;sub&gt;60&lt;/sub&gt;polymeric structures in Pt/C&lt;sub&gt;60&lt;/sub&gt;-2 favors water adsorption, and the shell-like charge redistribution around the Pt-bonding region induced by the curved surfaces of two adjacent C&lt;sub&gt;60&lt;/sub&gt;facilitates the desorption of hydrogen, thus favoring fast reaction kinetics for hydrogen evolution.&lt;/p&gt;</dc:description><dc:publisher>Nature</dc:publisher><dc:date>2023-12-01</dc:date><dc:nsf_par_id>10481623</dc:nsf_par_id><dc:journal_name>Nature Communications</dc:journal_name><dc:journal_volume>14</dc:journal_volume><dc:journal_issue>1</dc:journal_issue><dc:page_range_or_elocation/><dc:issn>2041-1723</dc:issn><dc:isbn/><dc:doi>https://doi.org/10.1038/s41467-023-38126-z</dc:doi><dcq:identifierAwardId>1801317</dcq:identifierAwardId><dc:subject/><dc:version_number/><dc:location/><dc:rights/><dc:institution/><dc:sponsoring_org>National Science Foundation</dc:sponsoring_org></record></records></rdf:RDF>