IP Library › Granted Patent US 12,631,557
Granted Patent B2
US 12,631,557 · App. 18/071,597 · Granted May 19, 2026

Equilibrium plasmonic analyte sensing apparatus and methods

Inventors: Jay James (Berkeley, CA); Jeffrey Scott Crosby (Richmond, CA)
Assignee: Picoyune, LLC
G01N21/554G01N33/0045
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 12,631,557
App. No.
18/071,597
Granted
May 19, 2026
Kind
B2
Abstract

Apparatus and methods are provided for quantitative detection of mercury vapor in gas samples using a film of nanoparticles. The localized surface plasmon resonance (LSPR) of an amalgam nanoparticle is sensitive to adsorbed mercury mass. The equilibrium mass of mercury on a gold nanoparticle is a function of the surrounding vapor concentration and the temperature of the gold. A device that introduces a temperature-controlled gold nanoparticle film to a controlled flow of sample gas responds predictably to a given mercury vapor concentration when optically probed in situ. Controlling the temperature of the film allows for control of adsorption and desorption rates. Equilibrium plasmonic mercury detection, described herein, removes the cycling necessary for many gold-based mercury analyses. Methods are given for the operation and analysis of the temperature-stabilized gold nanoparticle mercury sensor. The disclosed mercury-detection apparatus and methods find use in a variety of applications, including, for example, mercury detecting applications.

Claims (35)

1 . An analyte detection system, comprising:

(a) a flow cell comprising a multi-pass plasmonic sensor; wherein the multi-pass plasmonic sensor comprises:

(i) a first transparent substrate comprising a first mirrored surface; and an analyte-sensitive film disposed on a surface region of the first substrate, wherein the analyte-sensitive film comprises a plurality of metallic nanoparticles having an affinity for a selected analyte of interest;

(ii) a second substrate comprising a second mirrored surface in confronting spaced relation, on the order of millimeters, proximate to the first mirrored surface; and

(iii) a cavity region interposing the first and second mirrored surfaces;

(b) a light detector configured for detecting a localized surface plasmon resonance (LSPR) signal from the analyte-sensitive film

(c) a light source for directing a beam of light along a beam path that (i) enters the cavity region, (ii) impinges the analyte-sensitive film on the first substrate and reflects off the first mirrored surface, (iii) impinges and reflects off the second mirrored surface, (iv) again, impinges the analyte-sensitive film on the first substrate and reflects off the first mirrored surface, and (v) exits the cavity region enroute to the detector; and

(d) a temperature-control unit adapted to regulate the temperature of the analyte-sensitive film to a selected temperature;

wherein, the system can determine whether the analyte is present in a sample based on a LSPR signal detected from the analyte-sensitive film.

2 . The system of claim 1 , wherein, following steps (c) (i) and (c) (ii), each of steps (c) (iii) and (c) (iv) occur multiple times before step (c) (v) takes place.

3 . The system of claim 1 , wherein the analyte comprises a heavy metal.

4 . The system of claim 3 , wherein the heavy metal comprises mercury.

5 . The system of claim 1 , wherein the nanoparticles comprise an alloy.

6 . The system of claim 5 , wherein the alloy comprises an amalgam.

7 . The system of claim 1 , wherein the nanoparticles are preconditioned to substantially preclude irreversible analyte adsorption during use with said sample at the selected temperature of the analyte-sensitive film.

8 . The system of claim 1 , further comprising a gas source in communication with the flow cell and configured to provide a flow of a gas through the flow cell; and further wherein the sample is a gaseous sample.

9 . The system of claim 1 , wherein the light source comprises a visible light source.

10 . The system of claim 9 , wherein the system is configured to detect changes in optical absorbance in a single active band of the visible light spectrum.

11 . A method for determining whether a selected analyte is present in a gaseous sample, the method comprising:

(a) contacting a sample to an analyte sensor comprising:

(i) a first transparent substrate comprising a first mirrored surface; and an analyte-sensitive film disposed on a surface region of the first substrate, wherein the analyte-sensitive film comprises a plurality of metallic nanoparticles having an affinity for a selected analyte of interest;

(ii) a second substrate comprising a second mirrored surface in confronting spaced relation, on the order of millimeters, proximate to the first mirrored surface; and

(iii) a cavity region interposing the first and second mirrored surfaces;

(b) regulating the temperature of the analyte-sensitive film to a selected temperature;

(c) while performing step (b):

(i) directing light along a first path extending through the transparent substrate into the cavity region and onto the analyte-sensitive film, then reflecting off the first mirrored surface and extending to the second mirrored surface, reflecting off the second mirrored surface onto the analyte-sensitive film again, and finally exiting the cavity region;

(ii) detecting a localized surface plasmon resonance (LSPR) signal from the analyte-sensitive film; and

(d) determining whether the analyte is present in the sample based on a LSPR signal detected from the analyte-sensitive film.

12 . The method of claim 11 , wherein step (d) includes monitoring changes in transmission through the analyte-sensitive film in a single band or multiple bands of the visible spectrum.

13 . The method of claim 11 , wherein step (d) includes integrating detected steady-state LSPR signal with time.

14 . The method of claim 11 , further comprising the step of preconditioning the nanoparticles of the film to substantially preclude irreversible analyte adsorption during use with said sample at the selected temperature of the analyte-sensitive film.

15 . The method of claim 11 , wherein the analyte comprises a heavy metal.

16 . The method of claim 15 , wherein the heavy metal comprises mercury.

17 . The method of claim 16 , wherein the metallic nanoparticles comprise an amalgam.

18 . The method of claim 11 , wherein the sample comprises at least one of a gas or liquid.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 22, 2026
From: JAMES, JAY; CROSBY, JEFFREY SCOTT
To: PICOYUNE, LLC
Reel/Frame 074445/0381 →
Continuity (6)
Continuation In Part 17197805 · Mar 10, 2021
Continuation 16807374 · Mar 3, 2020
Division 16377124 · Apr 5, 2019
Provisional Application 63283989 · Nov 29, 2021
Provisional Application 62653555 · Apr 5, 2018
Related Publication 20240159671A1 · May 16, 2024
References Cited (20)
US 7456972B2 · Ke · 2008 [cited by examiner]
US 7486400B2 · Saito · 2009 [cited by examiner]
US 9291557B2 · James · 2016 [cited by examiner]
US 9322823B2 · Denomme · 2016 [cited by examiner]
US 10620122B2 · James · 2020 [cited by examiner]
US 10794904B2 · Denomme · 2020 [cited by examiner]
US 20060197952A1 · Chen · 2006 [cited by examiner]
US 20060197953A1 · Perez · 2006 [cited by examiner]
US 20080037022A1 · Nishikawa · 2008 [cited by examiner]
US 20110267621A1 · Nakatani · 2011 [cited by examiner]
US 20120021524A1 · Van Hal · 2012 [cited by examiner]
US 20120188551A1 · Langhammar · 2012 [cited by examiner]
US 20120257198A1 · Yamada · 2012 [cited by examiner]
US 20120257204A1 · Walters · 2012 [cited by examiner]
US 20120327417A1 · Amako · 2012 [cited by examiner]
US 20130182258A1 · Amako · 2013 [cited by examiner]
US 20140333933A1 · James · 2014 [cited by examiner]
US 20150124258A1 · Amako · 2015 [cited by examiner]
US 20190310192A1 · James · 2019 [cited by examiner]
EP 3121587A1 · 2017 [cited by examiner]