BEGIN:VCALENDAR
VERSION:2.0
PRODID:-//UCLA - ECPv5.14.1//NONSGML v1.0//EN
CALSCALE:GREGORIAN
METHOD:PUBLISH
X-WR-CALNAME:UCLA
X-ORIGINAL-URL:https://www.chemistry.ucla.edu
X-WR-CALDESC:Events for UCLA
REFRESH-INTERVAL;VALUE=DURATION:PT1H
X-Robots-Tag:noindex
X-PUBLISHED-TTL:PT1H
BEGIN:VTIMEZONE
TZID:America/Los_Angeles
BEGIN:DAYLIGHT
TZOFFSETFROM:-0800
TZOFFSETTO:-0700
TZNAME:PDT
DTSTART:20240310T100000
END:DAYLIGHT
BEGIN:STANDARD
TZOFFSETFROM:-0700
TZOFFSETTO:-0800
TZNAME:PST
DTSTART:20241103T090000
END:STANDARD
END:VTIMEZONE
BEGIN:VEVENT
DTSTART;TZID=America/Los_Angeles:20240110T160000
DTEND;TZID=America/Los_Angeles:20240110T170000
DTSTAMP:20260614T144139
CREATED:20240108T175429Z
LAST-MODIFIED:20240108T175506Z
UID:31984-1704902400-1704906000@www.chemistry.ucla.edu
SUMMARY:Inorganic Chemistry Student Exit Talk: Aamir Shah
DESCRIPTION:Flyer: Aamir Shah Flyer \nTitle: Fundamental Understanding of Electrode-Electrolyte Interface in Hydrogen Evolution Reaction (HER) Kinetics \nAbstract: Abstract: The hydrogen evolution reaction (HER) is one of the most fundamental and critical reactions in renewable energy conversion. The recent advancement in various platinum (Pt) nanocatalyst designs has led to greatly improved HER activity. Identification of the exact active sites and understanding the structure-activity relationship are critical for rational catalyst design but remain elusive due to the lack of methods robustly resolving the role of different surface sites. Moreover\, it is well recognized that the HER kinetics is drastically slower in alkaline media compared to acidic media\, but the descriptors of the HER kinetics are still elusive. Specifically\, in the presence of alkali metal cations and hydroxyl anions\, the electrode–electrolyte (platinum–water) interface in an alkaline electrolyte is far more complex than that in an acidic electrolyte. The effects of different alkali metal cations (AM+) and pH on these reactions are poorly understood due to a lack of suitable experimental methods. We are combining surface-sensitive electrical transport spectroscopy (ETS) with other electrochemistry techniques and computational studies to probe and understand the fundamental role of different AM+ and pH on the reaction kinetics of HER. Our study provides fundamental insights into how and why AM+ and pH influence the HER in alkaline media. We expect that this research will provide the molecular-level understanding that will shed new insights into electrolyte engineering as an alternative pathway to control electrochemical reaction kinetics.
URL:https://www.chemistry.ucla.edu/events/inorganic-chemistry-student-exit-talk-aamir-shah/
LOCATION:Mani L. Bhaumik Centennial Collaboratory\, 607 Charles E. Young Dr.\, East\, Los Angeles\, CA\, 90095\, United States
CATEGORIES:Inorganic Chemistry
END:VEVENT
END:VCALENDAR